CA2065866A1 - Production of growth hormone in transgenic animal milk - Google Patents

Abstract

DNA coding for human growth hormone was linked to mouse whey acid protein promoter fragment and microinjected into fertilized mouse ova. Females of the resulting transgenic mice were mated. After completion of gestation and birth of the litter, the milk from the mothers was assayed and found to contain human growth hormone.

Description

9 l ~(~3--- I Pcr/US90/051 3~) PRODUCIlON OF GROWTH HORMONE IN l~ANSGENIC ANIMAL MILK

Background of the Invention S This generally relates to the production of growth honnone in the milk of transgenic mammals.
Human growth hormone (hGH) is one member of the cascade of hormones responsible for normal growth in vertebrates.
The cascade is initiated when, in response to neurological stimulation, the hypothalmus is induced to release either a positive growth factor called growth hormone releasing factor (GHRF~, or a negative factor, called somatostatin. GH~F stimulates the pituitary to release growth hormone (GH), which in turn acts on the liver to produce insulin-like growth &ctor I. This in turn binds to receptors on the cells of peripheral tissue to modulate growth. Somatostatin acts on the pituitary to inhibit release of growth horomone.
In normal humans this cascade effectively modulates growth during childhood, usually resulting in adults of normal stature.
However, there at least are two cases in which nonnal statures are not attained. In one case, the short children are deficient in endogenous GH, probably as a result of some genetic defect. Administration of exogenous GH is effective in overcoming this deficiency in most of these individuals. In the other case, children of short stature have normal levels of endogenous GH, and thus are probably somewhat resistant to the effects of exogenous GH. Although one might expect treatment in-volving adrninistering exogenous hGH to be useless in these individuals, a study done at Emory University, reported by Shiner, G., Research Resources Reporter, U.S. Dept. Health and Human Selvices, vol. IV, pg 1-5 (1980), demonstrated that about 30~o of these children are responsive to exogenous hGH treatment. After this study was conducted, Rudman, et al, reported in Journal of Clinical Endocrinology and Metabolism, 49, 92-99 (1979), that the endogenous GH in the subset of short stature children who were responsive to the exogenous GH was defective in its ability to bind GH receptors. This study effectively enlarged the population of short stature children who could be helped by hGH treatment.

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~ 91/03~1 PCr/VS90/OS130 Z~ 9 -2-Besides its use as a treatment for short stature in some children, new evidence has emerged which suggests a role for GH in imrnunoregulation. Kelsey, et al, reported in N~usleic Acids Research 15, 1459-1474 (1987), that GH can stimulate macrophages to produce 5 more than double the normal amounts of superoxide anion (o2-~ in rats. Superox~de anion is one of the intermediates responsible for intracellular killing of pathogenic rnicrobes by macrophages, a function that is also carried out by interferons. Since macrophages are central to the induction and expression of many immune responses, the 10 discovery that GH acts on these macrophages in this way could lead to the discovery of other important macrophage activating properties of GH.
Other potential clinical applications of hGH include use in enhanced healing of wounds, cartilage darnage and fractures, and 15 treatment of burn trauma, stress ulcers, hypercholesterolerrua and osteoporosis.
Because growth horrnone is species specific, hGH has been available only in limited quantities as a purification product from the pituitaries of human cadavers. Although the recent cloning and the 20 expression of this cloned gene in bacteria has increased availability of hGH, as first reported by Martial, et al., Science 205, 602-606 (1979), the relatively low yield and purification difficulties have caused the price of hGH treatment to be between $8,000 and $30,000 per patient per year. Clearly a cheaper, more efficient way o-f producing hGH
25 with higher yield would be beneficial both for patients and for use in the initiation of new studies to test for additional properties of hGH.
A proposed alternative method of production of GH is through expression in transgenic animals. Unfortunately, expression of ;the hormone in transgenic animals incorporating the gene for growth 30 hormone has had a number of unexpected side effects. Por example, in pigs containing the gene for bGH in combination with an inducible metallothionein promoter, as described by Ramabhadran, et al., in . - . - . .. . . . . ~ .
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Gene 38, 111-118 (1985), the animals suffered from severe early onset rheumatoid arthritis. Transgenic mice having the gene for hS:~H fused with mouse metallothionein I promoter were infertile, as reported by ~ Bartke, et al., J,Experimental Zoo. 248, 121-124 (1988). See also Kyung-Kwang, et al., Korean J. Anim. Sci. 31(3), 139-147 (1989).
One way to avoid the systernic effects and increase purification yield is to create transgenic animals incorporating the gene for GH in combination with a tissue specific promoter, for example, a cost effective alternative to production of recombinant hGH in bacteria would be its production in the rnilk of transger~ic farm animals. By attaching the gene of interest to a tissue specific promoter for a highly expressed gene product, one can achieve specific expression of the gene of interest in tissues appropriate to the regulatory sequences. Some of the methodologies for making tissue specific sequences, and the problems associated with it, such as the lack of correlation between expression in cell culture in vitro and in vivo expression and the effect of regulatory proteins normally expressed by the targeted tissues, are discussed by S.~ Camper in Biotechniques 5(7), 638, 641-643 (1987).
Despite the problems, the production of foreign proteins in transgenic animals is an attractive alternative to bacterial or tissue culture fermentation as a means of producing large arnounts of recombinant proteins. Successes have been reported, including the production of human alpha-1-anti-trypsin in mouse and sheep serum by Kelsey, et al. (1987), as well as the production of sheep beta-lactoglobulin and human t-PA in mouse milk by Simons, et al., Nature 328, 53~533 (1987) and ~ordon, et al., Biotechnolo~y 5, 1183-1187 (1987). Some proteins are present in milk at concentrations as high as 16 grarns per liter, as reported by Clark, et al., Trends in Biotechnology, 5, 2~24 (1987).
It is impossible to predict whether it is possible to minuc these high levels by placing the hGH gene under control regions for .

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milk proteins which are selectively expressed in mammary tissues.
However, even at 10% efficiency the expression levels could be as high as 1.6 grarns per liter, which is significantly higher than current production levels in either bacteria or marnrnalian cell systerns.
S It is therefore an object of the present invention to provide transgenic animals capable of tissue specific expression of grouth hormone, especially human growth hormone.
It is a further object of the invention to provide transgenic animals which stably transmit the gene for expression of growth hormone in their milk.
It is a still further obect of the invention to provide vectors and regulatory sequences for expression of growth hormone, especially human growth hormone, for use in creating transgenic ar~imals capable of tissue specific expression of the growth ho~none.
Summary of the Invention DNA coding for human growth hormone (hGH) was linked to mouse whey acid protein promoter fragment and microinjected into fertilized mouse ova. Females of the resulting transgenic rnice were mated. After completion of gestation and birth of the litter, the milk from the mothers was assayed and found to contain hGH protein.

Brief Description of ~he Drawings Figure 1 is a schematic of the construction of the pWAPhGH fusion vector, containing the WAP tissue specific promoter in combination with the gene for hGh.

Detailed Description of the Invention The construction of transgenic mice expressing human growth hormone in their mammary glands which can be isolated and purified for use as a pharrnaceutical is described in detail below can, with rninor variations, be used to incorporate the same genes and ~- . , . :
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~o 9l/03~ Pcr/ussn/o5l3o ~' tissue specific promoters into animals of others species, such as rats, rabbits, pigs, sheep, and cows, for expression and purification of human growth hormone. Similarly, genes for growth horrnones of other origin, such as bovine or porcine growth hormone, can be 5 incorporated into similar vectors and inserted into the genome of the desired species.
The production of the growth hormone in the transgenic animals has a number of advantages, including normal glycosylation and absence of bacterial contarninants, unlike recombinant growth lû hormone produced by bacterial fermentation processes.

Experimental Design ~nd Methods:
Vector Construction:
pmWAPI`SI, containing EcoRI-BarnHI fragment of mouse 15 WAP promoter obtained from Dr. Lothar Henr~ighausen and described by Pittices, et al., in Proc.Natl,Acad.Sçi, 85, 5874-5878 (1988), was cut with ~I and BarnHI and ligated to pOGH cleaved with uI and BamHI. pOGH contains the DNA sequences coding for hGH and its polyadenylation signal. The resulting plasmid 20 pWAPhGH was isolated after transformation into E. coli using the method of Maniatis, et al., Molecular Cloning: A Laboratory Manual (Cold Spring Harborj NY 1982) and screening with appropriate en~ymes such as EcoRI, BarnHI, SmaI, SphI, and XhoI. The results are shown in Figure 1.
Preparation of DNA for mieroinJection:
pWAPhGH was digested with EcoRI and the 4754 bp ~agment containing the WAPhGH fusion gene was isolated on l~o -agarose gel followed by electroelution in a dialysis bag, as described 30 by Maniatis, et al. (1982). The eluted DNA was precipitated, redissolved in water and puri~led by passing through an elutip-D
column as per the instructions of the manufacturer (Schleicher and .: . ` : ' ~VO(?1/~ 1 I'Cr/US90/05130 Schuell, Inc., Keene, NH). The purified DNA was dissolved in SmM
Tris (pH 7.4) and 0.1 mM EDTA at 3 ~g/ml concentration for microinjection.

S ~nimals and emblyos:
Mice were obtained from Charles River Laboratories, Boston, MA and Jackson Laboratories, Maine. Reagents such as bovine serum alburr~in, gelatin, and pronase were obtained from Sigma Chen~ical Co., St. Louis, MO. Hormones for superovulation, PMS and hCG, were obtained from Organon, Inc., NJ. Hyaluronidase was purchased from Sigma. Restriction enzymes were obtained from Biolabs, Bever]y, MA The micromanipulator made by Nara Shige, USA, Inc., Rairun Instruments Co., Woburn, MA, was used to rnicroinject DNA into the pronuciei. DMEM, ~etal bovine serurn, and DPBS were supplied by GIBCO Laboratories, Gaithersville, MD.
Procedures for embryo manipulation and rnicroinjection are described in "Manipulating the Mouse Emb3~o" by B. Hogan, F.
Costantini and E. Lacy (Cold Spring Harbor Laboratory, 1986). - -Mouse zygotes were collected from six week old females that have been superovulated with pregnant mares serum (PMS) follwed 48 hours later with human chorionic gonadotropin. PAmed females were placed with males and checked for vaginal plugs on the follow~ng - -morning. Pseudopregnant females were selected for estrus, placed with proven sterile vasectomized males and used as recipients.
Zygotes were collected and cumulus cells removed by treatment with ~;
hyaluronidase (1 mg/ml).
Pronuclear embryos were recovered from B6D2 female rnice mated to CDI males. Females were treated with pregnant mare serum, PMS, (5 IU) to induce follicular growth and human chorionic gonadotropin, hCG (51 U) to induce ovulation. Embryos were recovered in a Dulbecco's modified phosphate buffered saline (DPBS) .. . .
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and maintained in Dulbecco's modified essential medium (DMEM) supplemented with 10% fetal bovine serum.

Microiruection:
Microinjections were performed using Narishige micromanipulators attached to a Nikon diaphot microscope. Embryos were held in 100 microliter drops of DPBS under oil while being microinjected. DNA solution was microinjected into the largest visible male pronucleus. Successful injection was monitored by swelling of 10 the pronucleus.

Embryo transfer:
Immediately after injection embryos were transferred to recipient females, mature CDI rmice mated to vasectomized male CD
15 mice. Recipient females were anesthetized using 2,2,2-tribromoethanol. Paralumbar females were made to expose the oviducts and the emblyos were transformed into the ampullary region of the oviducts. The body wall was sutured and the skin closed with wound clips. Recipients were appropriately ear notched for 20 identification and maintained until parturition.

Sampling for DNA integration:
At three weeks of age about 2-3 cm long tail samples were excised for DNA analysis. The tail samples were digested by incubating overnight at 55C nutator in the presence of 0.7 ml S0 mM
Tris, pH 8.0, 100 mM EDTA, 0.5% SDS and 350 ~g of prokienase K
The digested material was extracted once with equal volume of phenol and once with equal volume of phenol:chloroform (1:1 mixture). The supernatants were mixed with 70 I l 3 M sodium acetate (pH 6.0) and the DNAs were precipitated by adding equal volume of 100% ethanol.
The DNAs were spun down in a microfuge5 washed once with 70~o ethanol, dried and dissolved in 100 ~L TE buffer (10 mM Tris, pH 8.0 and 1 mM EDTA). 10 to 20 ~1 of DNAs were cut with BamHI and .... . . .. .
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3.~1 PCr/US90/05130 2~ 35~j B~111 or EcoRI, electrophoresed on 1% agarose gels, blotted onto nitrocellulose paper and hybridized with 32P-labeled hGH DNA
sequences. Transgen~c animals were identified by autoradiography.

S Propagation of ~ransgenic mice:
At five weeks of age transgenic female mice were mated to CDI males. At five days following parturition nulk samples were taken and assayed for hGH. At six to seven weeks of age transgenic males were mated to two CDI females. The Fl litters were analyzed for transgene. Four positive females were kept and mated at five weeks of age. At five days following parturition rlulk samples were assayed for hGH.

Collection of milk:
Milk samples (5~200 ~1) were collected from anesthetized mice injected with 0.05 units of oxytocin, an inducer of lactation. The -milk was collected in a glass capillary with the aid of mammary palpation.

R~dioimmunoassay:
Human growth hormone produced in the mouse milk was assayed by an RL~ kit available commercially from Nichols Institute Diagnostics, SanJuan Capistrano, C~

After successful microinjection of DNA into 720 embryos 69 live offspring were born. Fourteen of these, four males and ten females, were found to be transgenic and carrying different number of copies of WAPhGH. The females were mated and, after parturition, their milk samples were collected and assayed for hGH. The assay results are tabulated as follows:

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PCT/~JS 90/05130 IP~A/US 08 OCT199l Table 1: Expression of hGH in milk of Transganic Mice.
Transgenlc female hGH in milk (nq/ml) Control nontransgenic mouse o <1 11 o 14 <1 26 <l <5 -~
Mouse #27 is producing hGH at the rate of 970 ng/ml (970 ~g/liter) in its milk. Embryos of transgenic mouse embryo WAP-hGH(1-49) were deposited on September 11, 1991 with the American Type Culture Collection, Rockville, MD., as ATCC
72007.
Stable lines of transgenic animals expression hGH in their milk are produced by mating the females expressing the - gGH in their milk at the highest levels and by mating the offspring of the transgenic males. Despite the relatively high cost of generating these transgenic animals, scale-up costs are relatively low. In addition to conventional breeding as a means of proliferating these production animals, artificial insemination and embryo transfer techniques can be employed to increase the number available for production purposes.
Modifications and variations of the present invention will be obvious to those skilled in the art from the foregoing detailed description of the invention. Such modifications and variations are intended to come within the scope of the appended claims.
We claim.

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Claims (8)

1. A transgenic mammal selected from the group consisting of mice, rats, rabbits, sheep, pigs, and cattle having incorporated into the genome of all of its somatic and germ cells the gene encoding growth hormone and a mammary tissue specific promoter, said gene expressed specifically by the mammary glands of a lactating female transgenic mammal.

2. The transgenic mammal of claim 1 wherein the growth hormone is human.

3. The transgenic mammal of claim 1 wherein the promoter is the Whey acid protein promoter.

4. The transgenic mammal of claim 1 wherein the mammal is a mouse having incorporated into its genome a gene for human growth hormone that is produced in the milk of a lactating mouse at levels of approximately 50 ng hGH/ml of milk or greater.

5. A method for making a transgenic mammal selected from the group consisting of mice, rats, rabbits, sheep, pigs, and cattle having incorporated into the genome of all of its somatic and germ cells the gene encoding growth hormone and a mammary tissue specific promoter, said gene expressed specifically by the mammary glands of a lactating female transgenic mammal comprising providing a vector containing the WAP promoter and nucleotide sequence encoding growth hormone, the promoter regulating expression of the growth homone encoding sequence in the milk of the transgenic mammal.

6. The method of claim 5 further comprising microinjecting the vector into the embryo of a mammal which is selected from the group consisting of mice, rats, rabbits, sheep, pigs, and cattle.

7. The method of claim 5 wherein the growth hormone is human.

8. The method of claim 6 further comprising testing the transgenic mammals for production of growth hormone in the milk of lactating females and mating the animals containing the highest levels of growth hormone in the milk.