CA2244204C - A plant nuclear scaffold attachment region which increases gene expression - Google Patents

Abstract

A nuclear scaffold attachment region isolated from a tobacco gene, and a method of making recombinant cells having increased levels of expression of foreign genes therein, are described. The method comprises transforming the cell with a DNA construct comprising in the 5' to 3' direction, a transcription initiation region, a structural gene positioned downstream from the transcription initiation region and operatively associated therewith, and a scaffold attachment region of the nucleotide sequence provided herein, positioned either 5' to the transcription initiation region or 3' to the structural gene. DNA constructs and vectors employed in carrying out the foregoing method are also discussed.

Description

"A PLANT NUCLEAR SCAFFOLD ATTACHMENT REGION WHICH INCREASES GENE
EXPRESSION"
This invention was made with Government support under USDA research grants #91-37301-6377 and 92-37301-7710. The Government may have certain rights to this invention.
Field of the Invention The present invention relates to a plant nuclear scaffold attachment region and to methods for increasing the expression of foreign genes in cells, along with DNA constructs for carrying out such methods.
Backcrround of the Invention The proteinaceous nuclear 'matrix' or 'scaffold' of cells plays a role in determining chromatin structure. Electron micrographs show that nuclear DNA is attached to this scaffold at intervals to produce a series of loops (Zlatanova and Van Holde, J. Cell Sci_ 103:889 (1992)). Scaffold Attachment Regions (SARs) are AT-rich genomic DNA sequences which bind specifically to components of the nuclear scaffold. See Boulikas, J.
Cell. Biochem. 52:14 (1993)_ These sequences are thought to define independent chromatin domains through their attachment to the nuclear scaffold. Both transcription and replication are thought to occur at the nuclear scaffold.
It has been shown that when SARs are included on both sides of a transgene the expression level in stably transfected cell lines may become proportional to transgene copy number, indicating that gene activity is independent of position in the chromosome (Bonifer et al., EMBO J. 9:2843 (1990); McKnight et al., Proc. Natl.
Acad. Sci. USA 89:6943 (1992); Phi-Van et al., Nol. Cell.

CA 02'244204 2005-O1-07 Biol. 10:2303 (1990)). Flanking a GUS reporter gene with yeast SARs has been reported to result in higher and less variable transgene expression in plant ceils. Allen et al. Plant Cell 5:603 (1993). However, variation between different transformants was not dramatically reduced, and high levels of expression were not seen in transformants containing many copies of the transgene.
Summary of the Invention In view of the foregoing, a first aspect of the present invention is an isolated DNA molecule having a nucleotide sequence of SEQ ID NO: 1.
A further aspect of the present invention is a DNA construct comprising a transcription initiation region, a structural gene, and a scaffold attachment region of SEQ ID NO:1.
A further aspect of the present invention is a DNA construct comprising, in the 5' to 3' direction, a transcription initiation region, at least one structural gene positioned downstream from the transcription initiation region and operatively associated therewith, and a scaffold attachment region having SEQ ID NO:1 positioned either 5' to the transcription initiation region or 3' to the structural gene.
A further aspect of the present invention is a plant cell containing a DNA construct as described in the preceeding paragraph.
Further aspects of the present invention are transformed plant cells containing a DNA construct as described above, and recombinant plants comprising such transformed plant cells.
A further aspect of the present invention is a method of making transgenic plant cells with increased CA 02f244204 2005-O1-07 -2a-expression of foreign genes. The method includes transforming a plant cell capable of regeneration with a DNA construct of the present invention.
A further aspect of the present invention is a method of making transgenic plant cells having increased expression of foreign genes therein, the method comprising:
providing a plant cell capable of regeneration;
and transforming the plant cell with a DNA
construct comprising, in the 5' to 3' direction, a transcription initiation region, at least one structural gene positioned downstream from the transcription initiation region and operatively associated therewith, and a scaffold attachment region of SEQ ID NO:1 positioned either 5' to the transcription initiation region or 3' to the structural gene.
A further aspect of the present invention is a method of making recombinant tobacco plant cells having increased expression of foreign genes. The method includes transforming a tobacco plant cell with a DNA
construct according to the present invention.
A further aspect of the present invention is a method of making a recombinant tobacco plant cells having increased expression of foreign genes therein, the method comprising:
providing a tobacco plant cell capable of regeneration; and transforming the tobacco plant cell with a DNA
construct comprising, in the 5' to 3' direction, a transcription initiation region functional in plant cells, at least one structural gene positioned downstream from the transcription initiation region and operatively -2b-associated therewith, and a scaffold attachment region of SEQ ID NO:1 positioned either 5' to the transcription initiation region or 3' to the structural gene.
A further aspect of the present invention is a DNA construct comprising, in the 5' to 3' direction, a transcription initiation region, at least one structural gene positioned downstream from the transcription initiation region and operatively associated therewith, and a scaffold attachment region of SEQ ID NO:1 positioned either 5' to the transcription initiation region or 3' to the structural gene;
which DNA construct is carried by a plant transformation vector.
A further aspect of the present invention is a transformed tobacco plant cell containing a heterologous DNA construct comprising, in the 5' to 3' direction, a transcription initiation region functional in plant cells, at least one structural gene positioned downstream from the transcription initiation region and operatively associated therewith, and a scaffold attachment region of SEQ ID NO:1 positioned either 5' to the transcription initiation region or 3' to the structural gene.
A further aspect of the present invention is a plant transformation vector carrying a DNA construct which includes a transcription initiation region, a structural gene, and a scaffold attachment region of SEQ
ID NO:1.

Brief Description of the Drawings Figure 1 provides a schematic comparison of SAR
sequence motifs in the 1167 base pair tobacco SAR (RB7 SAR) of the present invention (SEQ ID NO:1) and the 838 base pair yeast SAR (ARS-1), showing A boxes (A), T boxes (T), Drosophila topoisomerase II sites (O), ARS consensus sequences (R), and G exclusion regions (ATC tract of 30 bp) represented by the black side bars. Local AT-rich regions (>20 bp) are indicated by the dark hatched boxes (regions of 95% AT) or lighter hatched boxes (90-95% AT).
Figure 2A is a schematic of the selection plasmid pGHNCIO, where NPTII is the nptll gene from TnS, ocs T is the polyadenylation site/terminator from octopine synthase gene, and arrows P1 and P2 indicate the locations of the PCR primers used in the estimation of copy numbers.
Figure 2B is a schematic of the control expression plasmid pGHNCI2, where CaMV 35S is the cauliflower mosaic virus 35S promoter, GUS is the coding region of the E. coli ~i-glucuronidase gene, nos T is the poiyadenylation site/terminator from the nopaline synthase (nos) gene, and arrows P1 and P2 indicate the locations of the PCR primers used in the estimation of copy numbers.
Figure 2C is a schematic of the (+)SAR
expression plasmid pGHNCI1, where CaMV 35S is the cauliflower mosaic virus 35S promoter, GUS is the coding region of the E. coli ,C3-glucuronidase gene, nos T is the polyadenylation site/terminator from the nopaline synthase (nos) gene, Rb7 SAR is the tobacco SAR.of SEQ ID
NO:l, and arrows P1 and P2 indicate the locations of the PCR primers used in the estimation of copy numbers.
' Figure 3A is a restriction map showing the GATC
sites (vertical lines) for RB7 SAR(+) plasmid pGHNCI1 and ' 35 the SARI-) control plasmid pGHNCI2. A 501 base pair probe fragment from the CaMV 35S promoter is indicated below the restriction maps.

Figure 3B provides DNA gel blots of selected RB7 SAR(+) lines (left panel) and a control of plasmid pGHNCI2 (right panel), indicating DpnI, DpnII and Sau3A
digests. Arrows indicate molecular weights estimated from 1 kb markers.
Figure 3C is a DNA gel blot of selected SARI-) control lines showing Dpnl, DpnII and Sau3A digests.
Molecular weight estimates are indicated by arrows.
Fa.gure 4 plots GUS expression versus gene copy number for individual cell lines, where open squares represent RB7 SAR(+) transformants and closed triangles represent controls.
Figure 5 is a plot of NPT protein against gene copy number, where open squares represent RB7 SAR(+) transformants and closed triangles represent control lines.
Figure 6 incorporates data from Figures 4 and 5, re-plotted to compare the expression levels for each introduced gene. Open squares represent double RB7 SAR
transformants; closed triangles represent control lines.
Detailed Descript3.on of the 2nventa.on The present inventors have found that a SAR
(RB7 SAR) isolated from tobacco (SEQ ID N0:1) used in conjunction with a transgene can increase average expression pergene copy by more than 100-fold in stably transformed cell lines. The present tobacco SAR effect was found to be maximal at relatively low transgene copy number-s _ The loop domain model of chromatin organization predicts that SARs act as boundary elements, limiting the spread of condensed chromatin structures and blocking the influence of cis-regulatory elements in neighboring chromatin. Thus, if variation in transgene expression is mainly attributable to genomic position effects, the ' presence of flanking SARs should normalize expression per gene copy and substantially reduce variability among WO 97127207 PCT/LTS97l01278 _ _5_ independent transformants. Total gene expression should then vary in direct proportion to gene copy number.
Experiments with animal cell systems have supported this prediction. Grosveld et al. Cell 51:975 (1987); Stief et al. Nature 341:343 (1989); Bonifer et al., EMBO J. 9:2843 (1990); McKnight et al., Proc. Natl. Acad. Sci. USA
89:6943 (1992); Phi-Van et al., Mol. Cell. Biol. 10:2303 (1990) .
Recent evidence indicates that one or more 'gene silencing' phenomena also contribute to overall variability, especially in fungal and higher plant systems. Assaad et al., Plant Mol. Biol. 22:1067 (1993);
Finnegan and McElroy, Bio/Technology 12:883 (1994);
Flavell, Proc. Natl. Acad. Sci USA 91:3490 (1994) . In principle, position effects on transgene expression reflect pre-existing features of the insertion site, such as proximity to genomic enhancers and degree of chromatin condensation, while gene silencing results from homology-dependent interactions involving the transgene itself, although chromosomal location may influence the severity of these interactions.
While not wishing to be held to a single theory, the present inventors propose that a portion of the large SAR effects seen with the SARof the present invention reflect a reduction in the severity of gene silencing under conditions in which control transformants are severely affected. Homology-dependent gene silencing must be considered whenever multiple transgenes are present. Although best known in fungi and higher plants, silencing of multicopy insertions has recently been reported in Drosophila as well (borer and Henikoff, Cell 77:993 (1994)).
The predominance of multicopy insertions in the transformants reported herein may be one reason the ° 35 presently reported RB7 SAR effects vary from those reported by laboratories using Agrobacterium vectors for transformation. In four reports, a moderate increase in expression was reported along with a decrease in variation between transformants (Mlynarova et al., Plant Cell 7:599 (1995); Mlynarova et al, Plant Cell 6:417 (1994); Schoffl et al., Transgenic Res. 2:93 (1993); van der Geest et al, Plant J. 6:413 (1994)). Breyne et al., Plant Cell 4:463 (1992) reported a decrease in average gene expression. Direct DNA-mediated transformation frequently produces complex loci in which multiple transgene copies are integrated at a single genomic site.
Interactions among homologous sequences at a single locus are thought to increase the frequency of silencing, thus it would be expected that the transformants reported in the Examples herein would be more affected by silencing than those obtained with Agro.bacterium vectors that only occasionally produce multicopy events.
The present invention may be used to transform cells from a variety of organisms, including plants (i.e., vascular plants). As used herein, plants includes both gymnosperms and angiosperms (i.e_, mon.ocots and dicots). Transformation according to the present invention may be used to increase expression levels of transgenes in stably transformed cells.
The term "operatively associated," as used herein, refers to DNA sequences on a single DNA molecule which are associated so that the function of one is affected by the other. Thus, a transcription initiation region is operatively associated with a structural gene when it is capable of affecting the expression of that structural gene (i.e., the structural gene is under the transcriptional control of the transcription initiation region). The transcription initiation region is said to be "upstream" from the structural gene, which is in turn said to be "downstream" from the transcription initiation region.
DNA constructs, or "expression cassettes," of the present invention preferably include, 5' to 3' in the direction of transcription, a first scaffold attachment _7_ region, a transcription initiation region, a structural gene operatively associated with the transcription initiation region, a termination sequence including a stop signal for RNA polymerase and a polyadenylation signal for polyadenylation (e. g., the nos terminator), and a second scaffold attachment region. All of these regions should be capable of operating in the cells to be transformed. The termination region may be derived from the same gene as the transcription initiation or promoter region, or may be derived from a different gene. DNA
constructs of the present invention as described above may include either a single structural gene or more than one structural gene operatively associated with the transcription initiation region. A particular DNA
construct of the present invention includes, 5' to 3' in the direction of transcription, a first scaffold attachment region, a transcription initiation region, a first structural gene operatively associated with the transcription initiation region, a second structural gene operatively associated with the transcription initiation region, a termination sequence including a stop signal for RNA polymerase and a polyadenylation signal for polyadenylation (e. g., the nos terminator), and a second scaffold attachment region.
The scaffold attachment regions (or "SARs") used to carry out the present invention have the nucleotide sequence of SEQ ID NO: 1 provided herein (RB7 SAR). The RB7 SAR may be isolated from natural sources or may be chemically synthesized.
SARs are known to act in an orientation-independent manner. Poljak et al., Nucleic Acids Res.
22:4386 (1994). Genetic constructs of the present ' invention may contain RB7 SARs oriented as direct repeats in a single orientation (~ ~), direct repeats in the ' 35 opposite orientation (~ ~), or either of two possible indirect repeats (-~ <- or E -j) .

_g-The transcription initiation region, which preferably includes the RNA polymerase binding site (promoter), may be native to the host organism to be transformed or may be derived from an alternative source, where the region is functional in the host. Other sources include the Agrobacterium T-DNA genes, such as the transcriptional initiation regions for the biosynthesis of nopaline, octapine, mannopine, or other opine transcriptional initiation regions, transcriptional initiation regions from plants, transcriptional initiation regions from viruses (including host specific viruses), or partially or wholly synthetic transcription initiation regions. Transcriptional initiation and termination regions are well known. See, e_g., dGreve, J. Mol. Appl. Genet. 1, 499-511 (1983); Salomon et al., EMBO J. 3, 141-146 (1984); Garfinkel et al., Cell 27, 143-153 (1983); and Barker et al., Plant Mol. Biol. 2, 235-350 (1983).
The transcriptional initiation regions may, in addition to the RNA polymerase binding site, include regions which regulate transcription, where the regulation involves, for example, chemical or physical repression or induction (e.g., regulation based on metabolites or light) or regulation based on cell differentiation (such as associated with leaves, roots, seed, or the like in plants). Thus, the transcriptional initiation region, or the regulatory portion of such region, is obtained from an appropriate gene which is so regulated. For example, the 1,5-ribulose biphosphate carboxylase gene is light-induced and may be used for transcriptional initiation. Other genes are known which are induced by stress, temperature, wounding, pathogen effects, etc. ' Structural genes are those portions of genes which comprise a DNA segment coding for a protein, ' polypeptide, or portion thereof, possibly including a ribosome binding site and/or a translational start codon, _g_ but lacking a transcription initiation region. The term can also refer to introduced copies of a structural gene where that gene is also naturally found within the cell being transformed. The structural gene may' encode a protein not normally found in the cell in which the gene is introduced or in combination with the transcription initiation region to which it is operationally associated, in which case it is termed a heterologous structural gene. Genes which may be operationally associated with a transcription initiation region of the present invention for expression in a plant species may be derived from a chromosomal gene, cDNA, a synthetic gene, or combinations thereof. Any structural gene may be employed. Where plant cells are transformed, the 25 structural gene may encode an enzyme to introduce a desired trait, such as glyphosphate resistance; a protein such as a Bacillus thuringiensis protein (or fragment thereof) to impart insect resistance; or a plant virus protein or fragment thereof .to impart virus resistance.
The expression cassette may be provided in a DNA construct which also has at least one replication system. For convenience, it is common to have a replication system functional in Escherichia call, such as ColEl, pSC101, pACYC184, or the like. In this manner, at each stage after each manipulation, the resulting construct may be cloned, sequenced, and the correctness of the manipulation determined. In addition, or in place of the E. coli replication system, a broad host range replication system may be employed, such as the replication systems of the P-1 incompatibility plasmids, e.g., pRK290_ In addition to the replication system, there will frequently be at least one marker present, which may be useful in one or more hosts, or ' different markers for individual hosts. That is, one marker may be employed for selection in a prokaryotic host, while another marker may be employed for selection in a eukaryotic host, particularly a plant host_ The markers may be protection against a biocide, such as antibiotics, toxins, heavy metals, or the like; provide _ complementation, for example by imparting prototrophy to an auxotrophic host; or provide a visible phenotype through the production of a novel compound. Exemplary genes which may be employed include neomycin phosphotransferase (NPTII), hygromycin phosphotransferase (HPT), chloramphenicol acetyltransferase (CAT), nitrilase, and the gentamicin resistance gene. For plant host selection, non-limiting examples of suitable markers are ~-glucuronidase, providing indigo production, luciferase, providing visible light production, NPTII, providing kanamycin resistance or G4I8 resistance, HPT, providing hygromycin resistance, and the mutated aroA
gene, providing glyphosate resistance-.
The various fragments comprising the various constructs, expression cassettes, markers, and the like may be introduced consecutively by restriction enzyme cleavage of an appropriate replication system, and insertion of the particular construct or fragment into the available site. After ligation anal cloning the DNA
construct may be isolated for further manipulation. All of these techniques are amply exemplified ir_ the literature and find particularexemplification in Sambrook et al., Molecular Cloning: A Laboratory Manual, (2d Ed. 1989)(Cold Spring Harbor Laboratory, Cold Spring Harbor, NY).
Vectors which may be used to transform plant tissue with DNA constructs of the present invention include non-Agrohacterium vectors, particularly ballistic vectors, as well as vectors suitable for DNA-mediated transformation.
Microparticles carrying a DNA construct of the present invention, which microparticles are suitable for the ballistic transformation of a cell, are also useful for transforming cells according to the present invention. The microparticle is propelled into a cell to produce a transformed cell. Where the transformed cell is a plant cell, a plant may be regenerated from the transformed cell according to techniques known in the art. Any suitable ballistic cell transformation methodology and apparatus can be used in practicing the present invention. Exemplary apparatus and procedures are disclosed in Stomp et al., U.S. Patent No. 5,122,466;
and Sanford and Wolf, U.S. Patent No. 4,945,050. When using ballistic transformation procedures, the expression cassette may be incorporated into a plasmid capable of replicating in the cell to be transformed. Examples of microparticles suitable for use in such systems include 1 to 5 ~m gold spheres. The DNA construct may be deposited on the microparticle by any suitable technique, such as by precipitation.
Agrobacterium tumefaciens mediated transformation methods, as are known in the art, may also be used to transform plant tissue with DNA constructs of the present invention.
Plant species may be transformed with the DNA
construct of the present invention by the DNA-mediated transformation of plant cell protoplasts and subsequent regeneration of the plant from the transformed protoplasts in accordance with procedures well known in the art.
Any plant tissue capable of subsequent clonal propagation, whether by organogenesis or embryogenesis, may be transformed with a vector of the present invention. The term "organogenesis," as used herein, means a process by which shoots and roots are developed sequentially from meristematic centers; the term "embryogenesis," as used herein, means a process by which -lla-shoots and roots develop together in a concertea fashion (not sequentially) , whether from somatic cells or gametes. The particular tissue chosen will vary depending on the clonal propagation systems available for, and best suited to, the particular species being transformed. Exemplary tissue targets include leaf disks, pollen, embryos, cotyledons, hypocotyls, megagametophytes, callus tissue, existing meristematic tissue (e. g., apical meristems, axillary buds, and root meristems), and induced meristem tissue (e.g.,'cotyledon meristem and hypocotyl meristem).
Plants of the present invention may take a variety of forms. The plants may be chimeras of transformed cells and non-transformed cells; the plants may be clonal transformants (e. g., all cells transformed to contain the expression cassette); the plants may comprise grafts of transformed and untransformed tissues (e.g., a transformed root stock grafted to an untransformed scion in citrus species). The transformed plants may be propagated by a variety of means, such as by clonal propagation or classical breeding techniques.
For example, first generation (or T1) transformed plants may be selfed to give homozygous second generation (or T2) transformed plants, and the T2 plants further propagated through classical breeding techniques. A
dominant selectable marker (such as npt II) can be associated with the expression cassette to assist in breeding.
Plants which may be employed in practicing the present invention include (but are not limited to) tobacco (Nicotiana tabacum), rapeseed (Brassica napus), potato (Solanum tuberosum), soybean (glycine max), peanuts (Arachis hypogaea), cotton (Gossypium hirsutum), sweet potato (Tpomoea batatus), cassava (Manihot esculenta), coffee (Cofea spp.}, coconut (Cocos nucifera), pineapple (Ananas comosus), citrus trees (Citrus spp.), cocoa (Theobroma cacao), tea (Camellia sinensis), banana (Musa spp.), avocado (Persea americana), fig (Ficus casica), guava (Psidium guajava), mango (Mangifera indica), olive (Olea europaea), papaya (Carica papaya), cashew (Anacardium occidentale), macadamia (Macadamia integrifolia), almond (Prunes amygdalus), sugar beets (Beta vulgaris), corn (Zea mays), wheat, oats, rye, barley, rice, vegetables, ornamentals, and conifers. Vegetables include tomatoes (Lycopersicon esculentum) , lettuce (e.g. , Lactuea sativa) , green beans (Phaseolus vulgaris), lima beans (Phaseolus Iimensis), peas (Pisum spp.) and members of the genus Cucumis such as cucumber (C. sativus), cantaloupe (C. cantalupensis), and musk melon (C. melo). Ornamentals include azalea (Rhododendron spp.), hydrangea (Macrophylla hydrangea), hibiscus (Hibiscus rosasanensis), roses (Rosa spp.), tulips (Tulipa spp.), daffodils (Narcissus spp.), petunias (Petunia hybrida), carnation (dianthus caryophyllus), poinsettia (Euphorbia pulcherima), and chrysanthemum. Gymnosperms which may be employed to variy i ng -~h° p Sent -- ~~'l~i~~'l~~~i1 -~~~1~~-~o111fCr5 V ut L11G r a including pines such as loblolly pine (Pines taeda), slash pine (Pines elliotii), ponderosa pine (Pines ponderosa), lodgepole pine (Pines contorta), and Monterey pine (Pines radiata); Douglas-fir (Pseudotsuga menziesii); Western hemlock (Tsuga canadensis); Sitka spruce (Picea glauca); redwood (Sequoia sempervirens);
true firs such as salver fir (Abies amabilis) and balsam fir (Abies balsamea); and cedars such as Western red cedar (Thuja plicata) and Alaska yellow-cedar (Chamaecyparis nootJcatensis) .
- The examples which follow are set forth to illustrate the present invention, and are not to be construed as limiting thereof.
' EXAMPLE 1 METHODS
1. Plasmid Constructs A GUS reporter plasmid was made by using a Klenow filled-in blunt-ended 1.1 kb ClaI/ScaI SAR

fragment (SEQ ID NO:1) from pRB7-6 (Hall et al., Proc.
Natl. Acad. Sci. USA 88:9320 (1991)), which was inserted into Klenow filled-in blunt-ended XbaI site in pBluescriptT"' II SK+ (Stratagene), resulting in plasmid pGHNCl. Similarly, the l.lkb ClaI/ScaI SAR fragment (SEQ
ID N0:1) was also inserted into the Klenow filled-in blunt-ended XhoI site in pBluescript II SK+ (Stratagene) resulting in pGHNC4. The l.lkb ApaI/HindIII fragment from pGHNC4 was then inserted into the ApaI/HindIII sites of pGHNCl to give pGHNC5. The 2.8 kb HindIII/EcoRI
fragment from pBI221 (Clonetech), containing the 35S
promoter/GUS reading frame/Nos terminator, was inserted into the HindIII/EcoRI sites of pGHNC5 or pBluescript II
SK+ to yield pGHNCll (+SARs) or pGHNCI2 (-SARs), respectively.
The selection plasmid (pGHNCIO) was created by ligating the HindIII/EcoRI fragment containing the nos promoter/NPT II reading frame/Ocs terminator from pUCNKl (Herrera-Estrella et al., IN: Gelvin et al. (Eds.), Plant Molecular Biology Manual, Kluwer Academic Publishers, Dordrecht, The Netherlands, pp. 1-22 (1988)) into the Hind III/EcoRI sites of pBluescript II SK+.
2. Microprojectile Transformation The Nicotiana tabacum cell line NT-1 was obtained from G. An, Washington State University.
Suspension cultures were grown in a medium containing Murashige and Skoog salts (GIBCO Laboratories, Grand Island, NY) supplemented with 100 mg/L inositol, 1 mg/L
thiamine HC1, 180 mg/L KHzP04, 30 g/L sucrose, and 2 mg/L
2,4-dichlorophenoxyacetic acid. The pH was adjusted to 5.7 before autoclaving. Cells were subcultured once per week by adding 3 ml of inoculum to 100 ml of fresh medium -14a-in 500 ml Erlenmeyer flasks. The flasks were placed on a rotary shaker at 125 rpm and 27'C with a light intensity of 47 ~,mol m zsec-1.

Four-day-old cells, in early log phase, were transformed by microprojectile bombardment. Aliquots of 50 ml were centrifuged and the pellet resuspended in fresh culture medium at a concentration of 0.1 g/ml.
Aliquots of 0.5 ml were spread as monolayers onto sterile lens paper which had been placed on culture medium solidified with 0.8% agar in_60 mm petri plates. Plated cells were kept at 23°C for 3h prior to bombardment.
Microprojectile bombardment was carried out with a DuPont PDS-1000 Particle Accelerator using a normal rupture disk valve of 1500 psi with the sample positioned 5.5 cm from the launch assembly.
Each batch of cells was co-transformed with a mixture of "expression" and "selection" plasmids . A ,Ci glucuronidase (GUS) gene driven by the CaMV 35S promoter (Benfey and Chua, Science 244:174 (1989)} was used to measure expression, while a neomycin phosphotransferase gene (nptl2) driven by the nopaline synthase promoter (Depicker et al., 1982) was used to select for cells which had stably integrated exogenous DNA. All plasmids were amplified in Escherichia co~i strain DHScx and isolated using a Quiagen plasmid maxiprep kit (Quiagen, Inc. Chatsworth, CA). Co-transformation mixtures contained a 4:1 molar ratio of GUS reporter plasmid to nptll selection plasmid. Therefore, each 500 ng SAR
transformation mixture consisted of 432 ng pGHNCll and 68 ng pGHNCIO, whereas control mixtures contained 314 ng pGHNCI2 and 68 ng pGHNCIO. Each DNA preparation (in 5 /.c.L
TE buffer) was mixed and precipitated with 50 /r.L of 2.5M
3 0 CaCl2 and 2-0 /.~.L of 0 . 1M spermidine onto 1 . 0 /~.m gold microprojectiles.
After bombardment, the petri plates were sealed with parafilm and incubated for 24 h at 27°C under constant light. Using the lens paper, cells were then transferred to fresh plates containing medium supplemented with 100 ~cg per ml kanamycin_ Isolated kanamycin resistant microcalli began to appear in approximately 3 weeks, at which time they were transferred to fresh plates containing kanamycin medium.
After 1 week's growth on plates, a suspension culture was started for each callus by inoculating 1 ml broth supplemented with 50 ~,g kanamycin per ml. Once established, the suspension cultures were transferred weekly using 3~ (v/v) inocula in 5 ml broth supplemented with 50 ~,g per ml kanamycin.
3. Gene Copy Number Analysis DNA was isolated as previously described (Allen et al., Plant Cell 5:603 (1993)). Estimates of GUS and nptll gene copy number were obtained for all cell lines by quantitative polymerase chain reaction (PCR) procedure, and confirmed for representative lines by genomic Southern analysis. The PCR procedure for GUS
gene copy number analysis used primers located in the CaMV35S promoter (5'-TCAAGATGCC TCTGCCGACA-3') (SEQ ID
N0:2) and in the translated region of the GUS gene (5'-TCACGGGTTG GGGTTTCTAC-3') (SEQ ID N0:3) and for nptll gene copy analysis used primers located in the nos promoter (5'-GGAACTGACA GAACCGCAAC-3') (SEQ ID N0:4) and in the translated region of the nptll gene (5'-GGACAGGTCG
GTCTTGACAA-3') (SEQ ID N0:5). A Hot Start PCR procedure using AmpliWaxT"" beads (Perkin Elmer) was used according to the manufacturer's instructions. The lower reaction mixture (25 ~,L) contained 0.8 mM dNTPs, 6 mM MgCl2, 0.4 mM
of each oligonucleotide primer, 50 mM KC1, 10 mM Tris-HC1 (pH 8.8). The upper reaction mixture (75 ~,1) contained 50 mM KC1, 10 mM Tris-HC1. (pH 8.8), 2.5U Tag Polymerase, and 100 ng genomic DNA in 10 ~.1 TE. Each cycle consisted of 2 min at 94'C, 2.5 min at 50'C, and 3 min at ?2'C.

-16a-Reactions were terminated following a final extension step of 7 min at 72'C.
PCR was limited to eighteen cycles for both the GUS and nptll copy number analysis to avoid substrate exhaustion, and amplification products were visualized by WO 97!27207 PCTIUS97/01278 blotting and hybridization with 32P-labeled DNA probe.
Reconstruction standards were prepared by serially diluting DNA from the pGHNCI1 (+SARs) into wild-type NT-1 genomic DNA so as to introduce between 1 and 150 GUS
genes per 1C (5 pg) equivalent of tobacco DNA
(Arumuganathan and Earle, 1991). PCR reactions were done simultaneously for standards and unknowns. Similarly, the nptll reconstruction standards were prepared by serially diluting DNA from the pGHNCIO into wild-type NT-1 genomic DNA so as to introduce between 1 and 40 nptll genes per 1C. Hybridization signals were quantified on an Ambis radioanalytical scanner (Ambis, San Diego, CA), and a final copy number estimates were calculated using linear regression analysis_ 4. DNA Gel Blot Analysis Southern analysis was done as described by Murray et al_ Plant Mol. Biol. Rep. 10:173 (1992).
Agarose gels were stained with 0.5 mg/ml ethidium bromide and photographed. The top 1/3 of the gels were treated with 0.25N HCl~ for 10 minutes. The gels were then incubated twice for 15 minutes in 150 mM NaOH.3mM EDTA, and twice for 15 minutes in 150mM NaPO~ pH 7.4, and blotted to Genescreen Plus (New England Nuclear) by the method of Southern (Sambrook et al., Molecular Cloning:
A Laboratory Manual, (2d Ed. 1989} Cold Spring Harbor Laboratory, Cold Spring Harbor, NY}.1989) using 25 mM
sodium pyrophosphate. The membranes were blocked by incubating in 2% SDS, 0.5% BSA, 1mM EDTA, 1mM 1,10-phenanthroline and hybridized in 100 mM NaP04 pH 7.8, 20mM
Na pyrophosphate, 5mM EDTA, 1mM 1,10-phenanthroline, 0.1%
SDS, 10 % dextran sulfate, 500 ~,cg/ml heparin sulfate, 50 ~.cg/ml yeast RNA, 50 /.cg/ml herring sperm DNA. Probes were prepared with the Random Prime DNA Labeling kit from United States Biochemical Co. Washing conditions included one wash at room temperature with 2X SSC, 0.5%
SDS for 5 minutes, one wash at room temperature with 2X

SSC, 0.1% SDS for 15 minutes, two washes at room temperature with O.1X SSC, 0.5% SDS for 15 minutes, and two washes at 37'C with O.1X SSC, 0.5% SDS for 30 minutes.
5. NPTII and GUS assays For NPTII protein assays cells were ground in liquid nitrogen and suspended in 100 JCL of 0.25M TrisCl, pH 7.8. The mixture was centrifuged and the supernatant was used for ELISA analysis using an NPTII ELISA kit (5'->3') according to the instructions of the manufacturer.
For GUS fluorometric analysis, frozen cells were ground in liquid nitrogen as described for the NPTII
and DNA extraction. Approximately 50 mg of the resulting powder was resuspended in 600 ~1 of GUS extraction buffer containing 50mM NaP04, pH 7.0, 10 mM ~i-mercaptoethanol, 10 mM Na2EDTA, 0.1% sodium lauryl sarcosine (w/v), and 0.1%
Triton X-1001"" (w/v) and sonicated twice for 10 sec. The extract was clarified by treatment with insoluble polyvinyl polypyrrolidone and centrifuged. GUS activity was determined by means of the fluorometric assay described by Jefferson, Plant Mol. Biol. Rep. 5:387 (1987); Jefferson et al., EMBO J. 6:3901 (1987), using methylumbelliferone glucuronide (MUG) as substrate.
Total protein was measured using the BioRad Protein assay kit (BioRad Laboratories, Melville, N.Y.) and GUS
specific activity reported as nmols 4-methyl umbelliferone (4-MU) formed ~min-1~mg protein-1 from the initial velocity of the reaction.

6. Transient Expression Protoplasts for electroporation were prepared from 4-day-old NT-1 suspension cultures by a procedure -18a-similar to that of Hall et al., Proc. Natl. Acad. Sci.
USA 88:9320 (1991). Cells from 100 ml of culture were harvested by centrifugation (300 X g for 2 min), washed twice in 100 ml of 0.4M mannitol, and resuspended in an equal volume of protoplasting solution containing 0.4M
mannitol, 20mM MES, pH 5.5, 1% cellulase (Onozuka RS) and 0.1°s pectolyase Y23 (Onozuka). They were then incubated at 25°C for 30-60 min with shaking at 150 rpm. The resulting protoplasts were washed twice in protoplast buffer containing 0.4M mannitol by centrifuging at 300 X
g for 5 min in a Beckman GPR centrifuge equipped with GH3.7 rotor. A protoplast concentration of 4 X 106 per ml was obtained by diluting the mixture with 0.4M mannitol.
The resulting suspension was then diluted by adding an equal volume of 2X electroporation buffer to a final concentration of 2 X 106 protoplasts per ml. The 2X
electroporation buffer contained 273mM NaCl, 5.36mM KCl, 2 . 94 mM KH2P04 , 15 . 5mM Na2HP04 , 0 . 4M mannitol , pH 6 . 5 .
Each electroporation used 80 fcg sheared E.coli carrier DNA and 20 ~.g of the plasmid DNA mixture to be tested. One ml of protoplast was added to the electroporation cuvette (BRL), mixed with 100 ~.L DNA
mixture in TE buffer, and left on ice fo.r 5 min.
Electroporation was done in a BRL Cell-Porator at 250V
and 1180 /.cF. Cuvettes were placed on ice for 15 min immediately after treatment. Aliquots (400 /.cl) of electroporated protoplasts were then transferred to 60 mm Petri plates containing 4 ml of culture medium with 0.4M
mannitol. After incubation for various time periods, protoplasts were collected by centrifugation at 300 X g for 5 min. at 4°C. Each pellet was suspended in 600 E.~.l GUS extraction buffer, and GUS activity was assayed by the fluorogenic procedure described above.
7. Isolation of Plant Nuclear Scaffold and Bindinct Assavs Nuclei and nuclear scaffolds from NT-1 cells were isolated as previously described (Hall et al., Proc.
Nat1_ Acad. Sci. USA 88:9320 (1991); Hall and Spiker, IN:
Gelvin et al. (Eds), Plant Molecular Biology Manual, Kluwer Academic Publishers, Dordrecht, pp. 1-12 (1994)).
The resulting nuclear halos were washed 2 times with WO 97!27207 PCT/US97/01278 Digestion/Binding Buffer (D/BB, pH 6.5) which contains 70mM NaCI; 20mM Tris, pH 8.0; 20mM KC1; O.lo digitonin;
1e thiodiglycol; 50mM spermine; 125 mM spermidine with 0.5mM PMSF and 2 ~.g ml-1 aprotinin (Hall et al., 1991;
Hall and Spiker, 1994). The halos were then washed again in the same buffer containing lOmM MgCla. The halos were then diluted to 4 X 106 ml-' in D/BB containing 0.5mM PMSF;
2 /.r,g ml-1 aprotinin; lOmM phenanthroline; and lOmM MgCl2;
and digested with 500 units ml-1 of the various restriction enzymes (New England Biolabs) at 37°C for 1h.
Fresh enzymes were then added and the incubation was continued for an additional lh. Aliquots (100 /.cl) containing scaffolds representing approximately 8 X 105 nuclei were centrifuged at 2600 X g, the supernatant was removed, and the scaffold pellets resuspended in D/BB
containing 0.5mM PMSF; 2 /.cg ml'1 aprotinin, and lOmM MgCla.
For binding assays, four fcmoles of 32P end labeled fragments previously digested with restriction enzymes (New England Biolabs), were added to the 100 j.cl scaffold aliquot along with appropriate competitor DNA
and incubated at 37°C for 3h with frequent mixings. The scaffold aliquots were centrifuged at 2600 X g and the pellet (containing scaffold-bound DNA fragments) and the supernatant containing non-binding fragments were separated. The pellet fraction was washed in.200 ~.l of D/BB with lOmM MgCl2, re suspended in 100 E.cl TE buffer (representing 1000) containing 0.5o SDS with 0.5 mg mi-1 proteinase K, and incubated at room temperature overnight. Equal fractions (usually 200) of pellet and supernatant fractions were separated on a to agarose gel in TAE buffer (Sambrook et al., 1989). The gel was treated with 7~ trichloroacetic acid for 20 min and dried onto filter paper followed by exposure to X-ray film.

EXAMPLE 2 ' SAR Motifs and Predicted Scaffold Binding Activit~r SARs are highly variable in sequence, however, several loosely defined SAR-related consensus elements or motifs have been identified from sequence comparisons in yeast and animal systems (Dickinson et al., Cell 70:631 (1992); Gasser et al., Int. Rev. Cytol. 119:57 (1989);
Gasser and Laemmli, EMBO J. 5:511 {1986); Mielke et al., Biochem. 29:7475 {1990))_ F=CURE 1 shows the distribution of some of these motifs in the 1186 base pair tobacco RB7 SAR (SEQ ID NO:1), and in an 838 base pair yeast SAR sequence (ARS-1, Allen et al., Plant Cell 5:603 (1993)).
In FIGURE 1, A boxes {A} were scored as an 8/10 or better match with the consensus sequence AATAAAYAAA, where Y=pyrimidine. T boxes (T) were scored as~a 9/10 or better match with the consensus TTWTWTTWTT, where W = A
or T. Drosophila topoisomerase II sites (O) were scored as a 13/15 or better match with the consensus GTNWAYATTN
ATNNG. ARS consensus sequences {WTTTATATTTW) are indicated by (R}. G exclusion regions (ATC tracts of 30 base pairs ) are represented by black side bars . Local AT-rich regions (>20 bp) are indicated by the dark hatched boxes (regions of 95% AT) or lighter hatched boxes (90-95o AT) .
The yeast SAR contains several A boxes and T
boxes. In addition, there is one ARS consensus element, two G-exclusion regions or ATC tracts of 30 bp, and a 20 by tract containing 90o A+T. The plant SAR (SEQ ID N0:1) contains a much higher density of A and T box motifs, AT-rich tracts, and G-exclusion regions, as well' as three elements with homology to the Drosophila topoisomerase II
consensus sequence. A systematic study of randomly cloned plant SARs (unpublished data) has not revealed a close correlation between any one of these motifs and binding activity in an in vitro assay. However, binding activity does correlate loosely with the total number or WO 97!27207 PCT/US97/O1Z78 overall density of SAR-related motifs. From this analysis and the data summarized in FIGURE l, it was predicted that a SAR of SEQ ID NO:l should bind to scaffold preparations much more strongly than the yeast SAR ( ARS - I ) .
EXAMPLE 3 ' Scaffold Binding Activit~r The RB7 SAR (SEQ ID NO:1) consistently showed a The binding activity of the tobacco RB7 SAR (SEQ ID
N0:1) was compared to that of the ARS-1 SAR. End-labeled restriction fragments from plasmids containing the SAR
sequences to be tested were mixed with tobacco nuclear scaffold preparations in the presence of restricted plant genomic DNA as nonspecific competitor. Plasmid pGA-1 contained the yeast SAR (ARS-1) and TRP1, and was digested with EcoRI and HINDIII. Plasmid pB7-5 Sca/Cla contained the RB7 tobacco SAR of SEQ ID N0:1, and was digested with SpeI and XhoI. After incubation with tobacco nuclear scaffold preparations under binding conditions, bound and unbound DNA fragments were separated by centrifugation, and DNA was purified prior to gel analysis.
Equal percentages (20%) of the pellet and supernatant from each reaction using plasmid pGA-1, as well as an equivalent aliquot of the unfractionated probe, were run on adjacent lanes of an agarose gel and visualized by autoradiography (results not shown). This same -procedure was replicated using a 10-fold lower percentage (2%) of the total and supernatant fractions loaded on the gel (results not shown) . A low level of binding by the yeast SAR was discernible in the gels using 20% of the fractions, although a large portion of the total signal was observed in the supernatant fraction when equal fractions were compared (results not shown).
In the more sensitive assay, it was clear that the yeast fragment bound while the TRP1 and vector fragments did not, confirming the specificity of theassociation between the SAR DNA and the isolated scaffold (results not shown) .
Similar autoradiography gels were prepared for plasmid pB7-6 Sca/Cla, containing the RB7 tobacco SAR of SEQ ID NO:l (results not shown). In contrast to the results obtained using the yeast SAR, above, a much larger portion of the tobacco RB7 SAR probe associated with the scaffold fraction (results not shown).
The possibility that elements other than known SARs might contribute to scaffold binding of the constructs used in expression assays was tested.
Scaffold binding assays similar to those described above were conducted on restriction digests designed to separate fragments containing the CaMV 35S promoter, the GUS gene, and the nos polyadenylation signal from the control plasmid, pGHNCI2. These binding assays gave uniformly negative results, even when the gel lanes were heavily overloaded with material from the pellet fraction (data not shown).
These results indicate that the RB7 SAR (SEQ ID
N0:1) has a higher binding activity than that of the yeast SAR (ARS-1).

RB7 SAR Increases Average Expression Levels Earl-ier studies (Allen et al., Plant Cell 5:603 (1993)) showed that flanking a GUS reporter gene with two copies of a yeast SAR element (ARS-1) increased average GUS expression by 12-fold in stably transformed cell lines. In the present Example, the same cell line was transformed with constructs similar to those of Allen et al. , 1993, but using the RB7 SAR (SEQ ID NO:l) . A co-transformation protocol was used to avoid physical linkage between the assayable and selectable markers (Allen et al., 1993). The constructs used are shown in FIGURES 2A, 2B and 2C.

Transformation was achieved by mixing the appropriate reporter test plasmid and the selection plasmid, co-precipitating them onto microprojectiles, and bombarding plates of tobacco suspension culture cells as described previously (Allen et al., 1993). Kanamycin-resistant (Kmr) microcalli were selected and each callus was used to start an independent suspension culture cell line, as described in Example 1. Histochemical staining of segments from the original microcalli showed that the staining intensity was much greater in cell lines transformed with SAR plasmids (data not shown) . After three weeks of growth, with weekly transfers, suspension cells were harvested. DNA was extracted from each cell line for Southern analysis and quantitative PCR assays, and portions of the same cell population were used to measure extractable GUS activity and NPT protein levels, as described in Example ~. Transgene copy number estimates and expression data are summarized in TABLES 1 and 2.
TABLES 1 and 2 also show the mean level of GUS
gene expression; measured as GUS enzyme activity, for the KMr lines. Control GUS activities averaged 8 nmol 4-MU
~min-'-~mg protein''-, well within the range of 1 to 54 nmol 4-MU ~min-'-~mg protein= commonly obtained for tobacco tissue transformed with similar constructs in Agrobacterium vectors (Frisch et al., Plant J_ 7:503 (1995); Hobbs et al., Plant Mol. Biol. 21:17 (1993);
Jefferson et al., EMBO J. 6:3901 (1987)}. When Rb7 SARs were ~.ncluded on both sides of the reporter gene, GUS
activities averaged approximately 60-fold greater than for the control construct lacking SARs. This effect on expression is approximately five-fold greater than that of the yeast SAR previously reported (Allen et al., 1993 ) .
TABLES 1 and 2 also show a comparison of average copy numbers for the GUS and nptll genes. These data were obtained with a quantitative PCR procedure (Allen et .al., 1993). In each case, amplification was carried out with primers corresponding to sequences in the promoter and coding regions, as described in Example 1. Appropriate PCR products were quantitated by counting the radioactivity hybridized to the amplified bands, and gene copy numbers were estimated by comparing the resulting signals with a standard curve obtained in parallel for each experiment. In cell lines transformed with the construct flanked by SARS, the average 35S::GUS
gene copy number was reduced by approximately two-fold compared to cell lines transformed with the control construct. This result is similar to that obtained in a previous study using the yeast SAR (Allen et al., 1993).
The fact that SAR-containing lines have fewer copies of the GUS gene means that the average RB7 SAR effect on expression per gene copy is even greater than the 60-fold increase in overall expression. As shown in TABLES 1 and 2, lines transformed with the RB7 SAR construct average nearly 140-fold more GUS enzyme activity per gene copy than lines transformed with the same construct lacking SARS.

NptII
Plasmid Cell GUS Gene GUS Gene NptII
Line Copy No.a ActivitybCopy No.a protein' Control 12-11 1 0.9 2 nd~
(-) SARS

12-9 1 2.5 2 42.9 12-46 1 0.9 2 18.4 12-48 2 1.4 2 nd I2-2 2 17.0 3 82.8 12-13 4 0.8 3 34.6 I2-23 4 0.3 3 37.5 12-1 5 0.5 3 nd 12-40 6 1.6 4 .108.5 12-36 11 1.2 3 63.6 12-25 12 48.4 8 50.0 12-10 29 0.7 4 80.4 I2-37 33 7.8 3 70.2 I2-I8 63 0.2 34 86.5 12-34 73 I3.0 14 76.4 12-41 77 33.5 10 46.1 Mean 20.2 8.2 6.2 6I.4 (+/- +/- 6.8 +/- 3.5 +/- 2.1 +/- 7.1 SE) Standard 27 14 8.I 25.5 Deviation Coeff. I.3 1.7 1.3 0.4 of Variation Gene copy numbers for GUS and Npt I I and expressi on 1 evel s for the individual transgenic tobacco lines derived from co-transformations of selection plasmid with control plasmid (-SAR).
a = Samples were analyzed for GUS and NptII gene copy number PCR assay (Example 1).
b = Samples were analyzed for GUS specific activity by fluorometric assay (Example 1).
c = The same samples used for GUS and gene copy numbers were analyzed for NptII protein by ELISA (Example 1).
d = not determined Coefficient of l7ariation = standard deviation/mean.

WO 97/27207 PCT/LTS97l01278 NptII
Plasmid Cell GUS Gene GUS Gene NptII
Line Co y No.a ActivitybCopy No.a protein' ' (+) SARS 11-36 1 0.8 2 2 Il-13 1 15.8 2 35.2 11-8 1 818.0 2 121.3 11-12 2 3.8 3 12.1 11-19 3 732.0 3 17.3 11-43 3 3109.0 4 53.9 11-1 5 341.0 3 40.2 lI-2 7 110.0 4 19.5 11-51 7 1241.0 8 124 lI-37 8 1006.0 5 90.9 11-7 9 189.0 3 46.6 11-41 10 113.0 3 24.8 11-38 I4 348.0 5 65.5 11-18 15 378.0 28 117 11-39 16 7.6 12 272.9 11-23 20 4.6 3 49.5 11-44 31 67.0 25 33.4 Mean 9 499 +/- 6.8 66.2 (+i- SE) +/- 2.0 188.2 +/- 1.9 +/- 15.9 Standard 8.1 776 - 7.8 65.7 Deviation Coeff. 0.9 1.6 l.I 1.0 of Variation ene copy m ers r U and pt I and xpression ve s for he i nu o N e e t of s ndividual ansgenictobacco es derivedrom co-transformations tr smid lin f election wit h plasmid AR.
pla +S

a = Samples were analyzed for GUS and NptII gene copy number PCR assay (Example 1).
b = Samples were analyzed for GUS specific activity by - fluorometric assay (Example 1).
c = The same samples used for GUS and gene copy numbers were analyzed for NptII protein by ELISA (Example 1).
Coefficient of Variation = standard deviation/mean.

Transient Expression To distinguish effects that depend on chromosomal integration from general transcriptional enhancer activity, SAR constructs were tested in a , transient expression system. Such assays are widely used in studies of transcriptional enhancers. Transiently transfected DNA is poorly organized into nucleosomes (Archer et al_, Science 255:1573 (1992); Weintraub Cell 42:705 (1985)) and the fact that only a small minority of expressing cells go on to become stably transformed suggests that most transient expression occurs without chromosomal integration (Christou, Plant J. 2:275 (1992);
Davey et al., Plant Mol. Biol. 13:273 (1989); Paszkowski et al., EMBD J. 3:2717 (1984); Saul and Potrykus, Develop. Genet_ 11:176 (1990}). When the plant SAR
plasmid (pGHNCll) was electroporated into NT-1 protoplasts prior to GUS assay 20 hours later, an approximately three-fold increase in GtIS gene expression was observed, from 2.7 to 7.2 nmol - min-1 - mg protein'1, as compared to those transfected with the control plasmid lacking SARs. These results are in sharp contrast to the nearly 60-fold increase :in overall expression, or the nearly 140-fold increase in expression per gene copy in stably transformed cell lines as reported in Example 5.
The effect of the RB7 element in stably transformed lines thus was 20-50 times greater than its effect in'transient transcription assays. These results indicate that the RB7 element is not simply acting as a transcriptional enhancer.

Intec;ration Patterns Direct gene transfer procedures can result in complex integration patterns (Christou Plant J. 2:275 (1992); Koziel et al., Bio/Technology 11:194 (1993);
Mittlesten Scheid et al. MoI. Gen. Geriet. 228:104 (1991) ;

Paszkowski et al., EMBO J. 3:2717 (1984); Tomes et al.
Plant Mol. biol. 14:261. (1990); Wan and Lemaux, Plant . Physiol. 104:37 (1994}). Therefore, multiple cell lines transformed with either the control expression plasmid (pGHNCI.2) or the RB7 SAR(+) expression plasmid (pGHNCIl) were compared by DNA gel blot analysis (according to Example 1) following digestion of isolated genomic DNA
with EcoRI and HindIII, which cut on either side of the 35S::GUS::nos cassette (see FIGURE 2).
Genomic DNA (10 fig) was digested with HindIII/EcoRI was fractionated on a 0.85% agarose gel.
The DNA was blotted to nylon membranes and probed as described in Example 1. Gel lanes contained 10 ~.~.g HindIII/EcoRI digested genomic DNA from the respective cell lines transformed with the SAR(+) or (-)SAR control plasmids. Also probed were copy number reconstruction gel lanes, containing 10 /.cg of non-transformed (control) genomic DNA spiked with the equivalent of 40, 20, 10, 5, 1 and 0 copies of the 2.8 kb 35S::GUS::nos T per 1C
equivalent.
When probed with sequences from the 35S
promoter, digests of the parent plasmids yielded a single band of 2.8 kb (data not shown). After integration into genomic DNA, complex hybridization patterns were observed, indicating extensive rearrangement during the integration process. Integration patterns for the control construct were somewhat more complex, on average, than those for the SAR plasmid. However, this difference may reflect the lower average copy number in the SAR
lines {see above). There was no obvious difference in the complexity of integration patterns for SAR and control lines with similar copy numbers.
Intact 2 . 8 Kb fragments containing the 35S : : GUS
gene were observed in most transformants, suggesting that most cell lines contained some non-rearranged gene copies. However, approximately 20 - 300 of the recovered lines lacked the 2.8 Kb band indicative of intact WO 97!27207 PCT/LTS97/OI278 35S::GUS genes. Generally this band was missing from lines with low overall copy numbers and with few, if any, bands with an intensity equal to or greater than the single copy reconstruction standard. Expression levels were generally very low; most ofthese lines likely contained genes with rearrangements- in the promoter region that reduced or eliminated their activity. One exception was the SAR line 37 (11-37), for which PCR
analysis gave an estimate of eight copies and Southern analysis showed several high molecular weight bands of multicopy intensity. This cell line also had high GUS
expression (TABLE 2), indicating that in this instance the rearrangement did not dramatically affect gene function.
Gel blots of unrestricted DNA samples were also probed (data not shown). Samples were selected to represent a variety of copy numbers and expression levels. Undigested DNA (5 ~cg) from cell lines, selected to include a wide range of gene copy numbers and expression levels, was fractionated on a 0.6a agarose gel and analyzed with a 501 by CaMV35S probe_ The position of high molecular weight chromosomal DNA was determined by ethidium bromide staining. The positions of undigested plasmid (pGHNCI1 and pGNHCI2) were determined.
Also probed were lanes representing 30, 10, 3 and 1 copies of the CaMV 35S::GUS::nos T per 1C, spiked in 5 ,ug of non-transformed genomic DNA.
In each case, all detectable GUS sequences migrated with high molecular weight chromosomal DNA, ruling out the possibility that they were maintained on extrachromosomal elements similar in size to the plasmids used in transformation. Similar results were obtained for lines with low and high overall copy numbers.
Chen et al., Plant J. 5:429 (1994) reported that transgenes in wheat cell lines subjected to direct DNA transfer may sometimes contain N-6-methyladenine, raising the possibility that transformation of an endophyte, such as a mycoplasma-like organism; occurred simultaneously with transformation of the wheat cells.
To exclude this possibility, a methylation analysis was carried out.
High molecular weight DNA from cell lines selected to include a variety of GUS gene copy numbers and expression levels was prepared and digested with the isoschizomers DpnI, DpnII, or Sau3A. DpnI requires N-6-adenine-- methylation; DpnII is inhibited by adenine methylation; Sau3A is unaffected by N-6-adenine methylation but inhibited by cytosine methylation.
FTGURE 3A is a restriction map showing the GATC sites (vertical lines) for SAR (+) plasmid pGHNCll and the SAR (-control plasmid pGHNCI2. The 501 base pair probe fragment from the CaMV~35S promoter is indicated below the restriction maps. FIGURE 3B is a DNA gel blot of selected SAR(+) lines showing DpnI, DpnII and Sau3A
digests. Molecular weights are estimated (arrows) from 1 kb markers (BRL). The control digest of plasmid pGHNCI2 which was produced from a Dam methylase (+) E.
col.i strain is shown in the right panel. F2GURE 3C is a DNA gel blot of selected SARI-) control lines showing DpnI, DpnII and Sau3A digests. Molecular weight estimates are shown by arrows to the left of the panel.
DpnI, which requires N-6-adenine methylation for activity, does not cut transgene DNA but does completely digest the same sequence in E. coli plasmid DNA used for transformation. DpnII, an isoschizomer that differs from DpnI in that it is inhibited by adenine methylation, does not cut the plasmid DNA, but extensively cleaves transgene sequences in all tested cell lines. Another GATC-cleaving isoschizomer, Sau3A
completely digests plasmid DNA, but shows only partial activity on transgene DNA. This enzyme is inhibited by cytosine methylation at the C residue in the GATC target sequence. In plant DNA, cytosine methylation occurs preferentially to CG and CXG sites in plant DNA

WO 97/27207 PCTlUS97/01278 (Gruenbaum et al., Nature 292:860 (1981)), although some methylation of cytosines also occurs in non-symmetrical positions (Meyer et al., Embo J. 13:2084 (1994)).
Failure of Sau3A to fully cleave transgene DNA is thus consistent with the presence of cytosine methylation at some of the GATC sites in the transgene. Taken together, these data indicate that adenine methylation. has been lost and a plant-specific pattern of cytosine methylation has been established during replication of the transgene in the transformed cell lines.

Cony Numbers and Exs~ression Levels GUS specific activity as nmols 4-MU produced ~min-1~mg protein-1 was determined by fluorimetry, and gene copy number was determined by the PCR procedure, for multiple transgenic cell lines eight weeks after transformation, as described in Example 1.
FIGURE 4 plots GUS expression versus gene copy number for individual cell lines (open squares .-- RB7 SAR(+) transformants; closed triangles =-control lines).
The largest RB7 SAR effects were obtained in cell lines with smaller numbers of transgenes (about 20 or fewer copies per cell), and expression of both SAR and control constructs was low in lines with high copy numbers.
Although the overall degree of stimulation was much greater for the plant SAR, the relationship to transgene copy number was quite similar to that previously observed in experiments with a weaker SAR from the yeast ARS-1 element (Allen et al., Plant Cell 5:603 (1993)).
Increased expression of the yeast SAR construct was seen in transformants carrying as many as 30-40 copies of the , transgene. In the present Example, the effects of the RB7 SAR were most evident in lines carrying fewer than about 20 copies.
Three cell lines (11-12, 11-13, and Il-36) containing the SAR construct at low copy number also showed low GUS expression, apparent exceptions to the general rule that low copy numbers are associated with high expression (TABLE 2). These lines were among those lacking the intact 2.8 Kb 35S::GUS::nos T band (see Example 7), and thus may contain only rearranged transgene sequences. These data have only a small effect on the overall data analysis, however. Eliminating data from the SAR and control lines lacking the 2.8 Kb band provides an average GUS activity of 574 nmols 4-MU ~min-=~mg protein-1 for lines containing the SAR construct as compared to 10 _ 4 nmols 4-MU ~min-'-~mg protein'1 for control lines, a 55-fold difference. Corresponding values for the entire data set were 499 and 8.2 nmols 4-MT7 ~min-I~mg protein-1, a 61-fold difference.

Effects of Co-Transformation on ExQression of Selection Gene In the present data, the Rb7 SAR of SEQ ID NO:1 increased expression to a greater degree when low numbers of the transgene were present and, when higher numbers of the transgene are present, expression of both SAR and control constructs fell. to low values. These data indicate that the present SARs were not acting as transcriptional insulators, and/or that variation from sources other than chromosomal position effects dominates transgene expression.
To determine whether co-transformat.i.on with a SAR-containing reporter plasmid resulted in increased expression of the nptT1 gene on the selection plasmid, the NPT protein levels in extracts of the same cell suspensions were measured using an ELISA assay. As shown in TABLE 2, co-transformation with the SAR-containing vector had no effect (1.1-fold) on average NPT protein abundance for all cell lines . NPTI I protein (pg/~.~.g total protein) was determined by ELISA, and gene copy number was determined by the PCR procedure for the transgenic cell lines used for GUS analysis (see F2GURE 4). F2GURE
is a plot of NPT protein against gene copy number (SAR(+) transformants - open squares; control lines closed triangles), showing that NPT2I expression was 5 unaffected by co-transformation with the SAR constructs.
NPTII protein levels vary widely in different transformants, up to about 100 pg/ug cellular protein.
The GUS and NPTII expression data from F=CURES 4 and 5 were re-plotted to compare the expression levels for each introduced gene (FIGURE 6). Open squares represent double SAR transformants; closed triangles represent control lines. Plotting GUS activity against NPT protein level showed that there is only a weak correlation between NPTII and GUS expression. Nearly all the NPT
values for SAR lines fall within the range of variation seen for control lines.
These results indicate that even though co-transformation often results in integration at the same genetic locus (Christou and Swain, Theo~. Appl. Genet.
79:337 (1990); Christou et al., Proc. Natl. ~lcad_ Sci.
USA 86:7500 (1989); McCabe et al., Bio/Technology 6:923 (1988); Christou, Plant J. 2:275 (I992); Saul and Potrykus, Develop_ Genet. 11:176 (1990)), genes on co-transformed plasmids can be substantially independent in their expression. If the reporter and selection plasmids were integrated in a closely interspersed array, SA.Rs on the GUS reporter construct might have also stimulated nptll gene expression. The lack of any such effect implies that the two plasmids normally do not integrate in a closely interspersed pattern, or that intervening plasmid sequences prevent the SARs from affecting other genes at the same chromosomal site. .

Recreneration of Transformed Nicotiana Using the same RB7 SAR constructs as used for suspension cell transformation experiments (Example 1.), Nicotiana tabaczzm has been transformed using microprojectile bombardment (see Example 1), and transformed plants have been regenerated.

Approximately 50 plants have been recovered from Double RB7 SAR transformation (SAR+); approximately 30 plants have been recovered from control transformation (lacking SARs). Primary transformants (mature TQ plants) were analyzed using Gus histochemical staining and using a PCR assay for the 35S GUS transgene. Preliminary data from the primary transformants indicates that:

(a) transformation with the_ SAR+ plasmid results in increased numbers of transformants;

(b) both SAR+ and control primary transformants have equal numbers of plants which contain 35S-GUS genes (as determined by quantitative PCR. assay) but which have no Gus expression (i.e., gene silencing in the primary transformants);

(c) there does not appear to be a difference in the number of transformants that stain positive for Gus;

measurements of Gus activity are in progress to determine whether there is an effect on absolute differences in the magnitude of Gus expression between the two. types of transformants. A comparison of Gus staining patterns suggests that the SAR-transformed plants are less subject to variegated expression in leaf punches.

Backcrosses of the experimental transformants to a wild-type Nicatiana (Petite havana) parent have been made. Tnitial data suggests that BC1 plants containing SAR-less transgene experience gene silencing 5-fold more than the BC1 plants from the SAR-containing transformants (data not shown). These results indicate that SARs may stabilize gene expression in future generations.

W~ 97/27207 PCT/US97/01278 Acarrobacterium tumefaciens mediated transformation of Brassica nanus ~ , Rapeseed (canola) cells were transformed using Agrobacterium tumefaciens mediated transformation. , Agrobacterium tumefaciens strains Z707S and LBA4404 were used. As shown in Table 3; each of the two strains of Agrobacterium was used to transform cells with a construct comprising two structural genes (Ubl/Hpt and 35S/GUS genes) and having either two flanking RB7 SARs or having no SARs. Regenerated plants were obtained. Table 3 summarizes the data obtained during transformation and regeneration, as well as GUS expression data from To plants.
Effect on transformation efficiency: The 27075 strain of Agrobacterium is normally more efficient at transforming rapeseed than the LBA4404 strain (see SAR-less control plasmid results in Table 3; ~42 vs. 2 hygromycin resistant calli for Z707S and LBA4404, respectively). When SARs flank the transgene no effect is seen on the number of hygromycin resistant calli from the Z707S strain (42 for the SAR-less Z707S control and 41 for SAR+ Z707S). However, the less efficient LBA4404 strain yields significantly more hygromycin resistant calli when SARs are present (2 vs. 15). These results indicate that SARs may have a beneficial effect on Agrobacterium mediated transformation of crop plants that have previously proved refractory to Agrobacterium transformation.
Effect on reportersene expression: The Ta SAR+
rapeseed plants yielded a 33-fold higher average GUS
expression compared to the SAR-less control plants. The highest GUS expressing SAR+ plant was 27-fold higher than the highest SAR-less plant. Southern blot analysis of these plants show them to contain high gene copy numbers (data not shown). This was surprising since Agrobacterium normally inserts only a few gene copies.

This effect appears not to be due to the SARs, since both SAR+ and SAR-less constructs were high copy number.
These data show:
(a) the SAR effect is amenable to Agrobacterium transformation;
(b) the SAR effect occurs in regenerated transgenic plants;
(c) SARs can exhibit their effect when flanking two genes (in the present case the Hpt selectable marker and the GUS reporter gene).
(d) RB7 SARs work in plant species other than tobacco.
The foregoing examples are illustrative of the present invention, and are not to be construed as I5 limiting thereof. The invention is described by the following claims, with equivalents of the claims to be included therein.

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SEQUENCE LISTING
(1) GENERAL INFORMATION:
(i) APPLICANT: North Carolina State University (ii) TITLE OF INVENTION: A PLANT NUCLEAR SCAFFOLD ATTACHMENT
WHICH INCREASES GENE EXPRESSION
(iii) NUMBER OF SEQUENCES: 5 (iv) CORRESPONDENCE ADDRESS:
(A) ADDRESSEE: Patricia A. Rae; Sim & McBurney (B) STREET: 330 University Avenue, 6th Floor (C) CITY: Toronto (D) STATE: Ontario (E) COUNTRY: CANADA
(F) ZIP: M5G 1R7 (v) COMPUTER READABLE FORM:
(A) MEDIUM TYPE: Floppy disk (B) COMPUTER: IBM PC compatible (C) OPERATING SYSTEM: PC-DOS/MS-DOS
(D) SOFTWARE: PatentIn Release #1.0, Version #1.30 (vi) CURRENT APPLICATION DATA:
(A) APPLICATION NUMBER: 2244204 (B) FILING DATE: January 24, 1997 (C) CLASSIFICATION:
(viii) PATENT AGENT INFORMATION:
(A) NAME: Rae, Patricia A.
(B) REFERENCE NUMBER: 9399-87 PAR
(ix) TELECOMMUNICATION INFORMATION:
(A) TELEPHONE: 416-595-1155 (B) TELEFAX: 416-595-1163 (2) INFORMATION FOR SEQ ID N0:1:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 1167 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: DNA (genomic) (xi) SEQUENCE
DESCRIPTION:
SEQ ID
N0:1:

(2) INFORMATION FOR SEQ
ID N0:2:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 20 base pai rs (B) TYPE: nucleic acid (C) STRANDEDNESS: singl e (D) TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA

(xi) SEQUENCE DESCRIPTION: SEQ ID N0:2:

(2) INFORMATION FOR SEQ ID N0:3:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:3:

(2) INFORMATION FOR SEQ ID N0:4:
(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 20 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:4:

(2) INFORMATION FOR SEQ ID N0:5:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:5:

Claims (26)

THAT WHICH IS CLAIMED IS:

1. An isolated DNA molecule having a nucleotide sequence of SEQ ID NO:1.

2. A DNA construct comprising, in the 5' to 3' direction, a transcription initiation region, at least one structural gene positioned downstream from said transcription initiation region and operatively associated therewith, and a scaffold attachment region having SEQ ID NO:1 positioned either 5' to said transcription initiation region or 3' to said structural gene.

3. A DNA construct according to claim 2, which construct comprises, in the 5' to 3' direction, a first scaffold attachment region of SEQ ID NO:1, a transcription initiation region, at least one structural gene positioned downstream from said transcription initiation region and operatively associated therewith, and a second scaffold attachment region of SEQ ID NO: 1.

4. A DNA construct according to claim 2 carried by a plant transformation vector.

5. A DNA construct according to claim 2 carried by an Agrohacterium tumefaciens plant transformation vector.

6. A plant cell containing a DNA construct according to claim 2.

7. A dicotyledonous plant cell containing a DNA construct according to claim 2.

8. A monocotyledonous plant cell containing a DNA construct according to claim 2.

9. A gymnosperm plant cell containing a DNA
construct according to claim 2.

10. A cell according to claim 6, wherein the DNA construct comprises, in the 5' to 3' direction, a first scaffold attachment region of SEQ ID NO:1, a transcription initiation region, a structural gene positioned downstream from said transcription initiation region and operatively associated therewith, and a second scaffold attachment region of SEQ ID NO:1.

11. A cell according to claim 10, wherein said construct further comprises a termination sequence positioned downstream from said structural gene and operatively associated therewith, said termination sequence positioned 5' to said second scaffold attachment region.

12. A plant cell according to claim 7, which cell is from a plant that is a divot selected from the group consisting of tobacco, potato, soybean, peanuts, cotton, rapeseed and vegetable crops.

13. A method of making transgenic plant cells having increased expression of foreign genes therein, said method comprising:

providing a plant cell capable of regeneration; and transforming said plant cell with a DNA construct comprising, in the 5' to 3' direction, a transcription initiation region, at least one structural gene positioned downstream from said transcription initiation region and operatively associated therewith, and a scaffold attachment region of SEQ ID NO:1 positioned either 5' to said transcription initiation region or 3' to said structural gene.

14. A method according to claim 13, which construct comprises, in the 5' to 3' direction, a first scaffold attachment region of SEQ ID NO:1, a transcription initiation region, at least one structural gene positioned downstream from said transcription initiation region and operatively associated therewith, and a second scaffold attachment region of SEQ ID NO:1.

15. A method according to claim 13, wherein said transforming step is carried out by bombarding said plant cell with microparticles carrying said expression cassette.

16. A method according to claim 13, wherein said transforming step is carried out by Agrobacterium tumefaciens transformation.

17. A method according to claim 13, wherein said plant cell resides in a plant tissue capable of regeneration.

18. A method according to claim 13, further comprising the step of regenerating shoots from said transformed plant cells.

19. A method according to claim 13, further comprising the step of regenerating roots from said transformed plant cells.

20. A method according to claim 13, further comprising the step of regenerating a plant from said transformed plant cells.

21. A method according to claim 13, wherein said plant cells are monocot cells.

22. A method according to claim 13, wherein said plant cells are divot cells.

23. A method according to claim 13, wherein said plant cells are gymnosperm plant cells.

24. A method of making recombinant tobacco plant cells having increased expression of foreign genes therein, said method comprising:
providing a tobacco plant cell capable of regeneration; and transforming said tobacco plant cell with a DNA
construct comprising, in the 5' to 3' direction, a transcription initiation region functional in plant cells, at least one structural gene positioned downstream from said transcription initiation region and operatively associated therewith, and a scaffold attachment region of SEQ ID NO:1 positioned either 5' to said transcription initiation region or 3' to said structural gene.

25. A DNA construct comprising, in the 5' to 3' direction, a transcription initiation region, at least one structural gene positioned downstream from said transcription initiation region and operatively associated therewith, and a scaffold attachment region of SEQ ID NO:1 positioned either 5' to said transcription initiation region or 3' to said structural gene;
which DNA construct is carried by a plant transformation vector.

26. A transformed tobacco plant cell containing a heterologous DNA construct comprising, in the 5' to 3' direction, a transcription initiation region functional in plant cells, at least one structural gene positioned downstream from said transcription initiation region and operatively associated therewith, and a scaffold attachment region of SEQ ID NO:1 positioned either 5' to said transcription initiation region or 3' to said structural gene.