WO2019195675A1 - Methods of identifying combinations of transcription factors - Google Patents

Abstract

Provided herein, in some embodiments, are methods and compositions for identifying combinations of transcription factors, for example, those involved in cell type conversion processes, such as cell differentiation.

Description

METHODS OF IDENTIFYING COMBINATIONS OF TRANSCRIPTION FACTORS

REUATED APPUI CATIONS

This application claims the benefit under 35 U.S.C. § 119(e) of U.S. Provisional Application Serial No. 62/653,576, filed on April 6, 2018, which is herein incorporated by reference in its entirety.

BACKGROUND

Cellular reprogramming plays a key role in the production of the various cell types needed for disease modeling, drug discovery, disease treatment and tissue engineering. As an example, stem cells can be differentiated into oligodendrocyte progenitor cells, myoblasts, neurons, cardiomyocytes, macrophages, hepatocytes, and blood progenitors for cell therapy. Although transcription factors are key regulators of cell identity, a single transcription factor is often not sufficient to induce cell differentiation. Instead a combination of transcription factors is usually required. Thus, there is a need to conduct large-scale overexpression analyses to identify transcription factor combinations in an unbiased manner.

SUMMARY

Provided herein, in some embodiments, are methods and nucleic acids for identifying transcription factor combinations for cellular reprogramming ( e.g ., stem cell differentiation). Although transcription factors are known modulators of cell identity, unbiased

characterization of transcription factor combinations are limited, in part due to the lack of efficient methods for associating a transcription factor combination with a particular cellular phenotype (e.g., transcriptome). The experimental results provided herein, however, show unexpectedly that barcoded transposon expression vector (e.g., barcoded piggyBAC^™ expression vector) of the present disclosure enables high resolution identification of transcription factor combinations driving a particular cell state, even in stem cells.

Accordingly, some aspects of the present disclosure provide a population of nucleic acids comprising a transposon carrying a cargo element that comprises a promoter operably linked to a sequence encoding a transcription factor and a barcode that is located within 100 nucleotides (e.g., 50 nucleotides) of a terminator sequence. In some embodiments, the transposon comprises terminal repeats (e.g., inverted terminal repeat sequences or long terminal repeat sequences) flanking the cargo element. In some embodiments, the terminal repeats are recognized by a transposase (e.g., a piggyBAC^™ transposase). In some embodiments, the nucleic acids encode more than one transcription factor and one barcode that uniquely identifies the combination of transcription factors encoded by the nucleic acid.

Other aspects of the present disclosure provide a cloning vector that includes terminal repeats flanking a promoter operably linked to a multiple cloning site and a barcode that is located within 100 nucleotides ( e.g ., 50 nucleotides) of a terminator sequence. In some embodiments, the cloning vector is a piggyBAC^™ cloning vector (i.e., a cloning vector that comprises piggyBAC^™ inverted repeat sequences). These vectors may be useful in high throughput production of the modified barcoded transposon vectors described herein.

Other aspects of the present disclosure provide a population of cells and each cell comprises a transposon carrying a cargo element that comprises a promoter operably linked to a sequence encoding a transcription factor and a barcode that is located within 100 nucleotides (e.g., 50 nucleotides) of a terminator sequence. In some embodiments, the transposon comprises terminal repeats (e.g., inverted terminal repeat sequences or long terminal repeat sequences) flanking the cargo element. In some embodiments, the terminal repeats are recognized by a transposase (e.g., a piggyBAC^™ transposase). In some embodiments, the nucleic acids encode more than one transcription factor and one barcode that uniquely identifies the combination of transcription factors encoded by the nucleic acid. In some embodiments, the cells further comprise a transposase. In some embodiments, the cell is a human cell. In some embodiments, the cell is a stem cell (e.g., an induced pluripotent stem cell).

Other aspects of the present disclosure provide methods that include introducing into cells (e.g., stem cells) a population of nucleic acids encoding a barcoded transcription factor expression transposon, detecting differences in gene expression in the cells to identify differentiated cells, and detecting at least one barcode to identify one or more transcription factors in the differentiated cells. In some embodiments, the cells comprise a transposase. In some embodiments, single cell RNA sequencing (e.g., droplet-based single cell RNA sequencing) is used to detect differences in gene expression. These methods may be used, for example, to analyze a library of transcription factors in an unbiased manner and identify combinations of transcription factors that induce stem cell differentiation.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGs. 1A-1D include a series of schematics depicting a piggyBAC^™ transcription factor (TF) expression vector that lacks a barcode and an initial transcription factor analysis in human induced pluripotent stem cells using this vector. FIG. 1A shows a schematic of the piggyB AC^™ expression vector without a barcode used in the initial transcription factor assay. Tet-On promoter refers to a doxycycline-inducible promoter. AttB 1 and AttB2 are Gateway recombinase-based cloning sites. TF ORF refers to transcription factor open reading frame. V5 tag is a short protein epitope tag to verify protein expression. T refers to a transcriptional terminator. The first transcriptional terminator is the BGH (bovine growth hormone) terminator. The second transcriptional terminator is the SV40 (simian virus 40) terminator. EF1 alpha is a constitutively active promoter. rtTA refers to a reverse tetracycline-controlled trans-activator. 2A is a self-cleaving peptide sequence that separates protein sequences. Puro^R is a gene that confers puromycin resistance. The diagram is not to scale. FIG. IB is a flowchart showing the experimental scheme of generating human induced pluripotent stem cells (hiPSCs) that overexpress TFs for single cell RNA sequencing. FIG. 1C is a pie chart showing the percentage of cells where the overexpressed TF could be detected (14.2%) compared to the percentage of cells where the overexpressed TF could not be detected (85.8%). FIG. ID is a schematic depicting an example of individual sequencing reads that map to the vector in FIG. 1A. This diagram is to scale, 100 base pairs.

FIG. 2 is a t-distributed stochastic neighbor embedded (t-SNE) projection of single cell RNA-sequencing results of human induced pluripotent stem cells (hiPSCs) without TF overexpression and shows expression of the endogenous, lowly expressed OCT4 TF. Each dot is a single cell. This pluripotency TF is expressed at low levels in cells, yet robust expression of this TF was detected in virtually all cells without modification to the protocol

FIG. 3 is a chart showing analysis of TF overexpression using population RNA sequencing. Error bars show standard errors of the mean. The transcription factors used were as follows: TF1 = ATOH1, TF 2 = NKX3-2, TF 3 = ETV2, TF 4 = MYOG, TF 5 =

NEUROG3, TF 6 = FOXC1, TF 7 = SOX14, TF 8 = HOXB6, TF 9 = WT1 and TF 10 = ZSCAN1.

FIGs. 4A-4E include a series of schematics showing design considerations for modifications in the piggyB AC^™ vector. FIG. 4A is a schematic showing four regions of the piggyB AC^™ vector considered for modification in the context of single cell RNA sequencing. NVT(30) refers to a random nucleotide (N), non-T base (V), 30 Ts T(30). FIG. 4B is a schematic showing design considerations within region 3 from FIG.4A. FIG. 4C is a schematic showing a region with high sequence identity, which prevents specific primer binding. Sequences correspond to SEQ ID NOs: 31-32 from top to bottom. FIG. 4D is a schematic showing a repetitive region, which prevents accurate primer binding. The sequence corresponds to SEQ ID NO: 33. FIG. 4E is a schematic showing a region of high homopolymer content, which reduces amplification efficiency. The sequence corresponds to SEQ ID NO: 34.

FIG. 5 is a schematic showing a barcoded piggyB AC^™ transcription factor expression vector. The location of the barcode is indicated as“address.” The elements of the vector are indicated as follows: ITR = 5’ and 3’ piggyB AC^™ inverted terminal repeats for integration into the genome, AttBl and AttB2 = Gateway recombinase-based cloning sites, Insulator = Transcriptional insulator sequence to prevent chromatin silencing, Tet-On = doxycycline- inducible promoter, TF = transcription factor open reading frame; Aarl = Aarl restriction enzyme recognition site, 2A = 2A cleaving peptide, Address = TF-specific barcode for single cell RNA-seq readout, T = transcriptional terminator, EF1 alpha = constitutively active promoter, rtTA = reverse tetracycline trans-activator and Puro^R= puromycin resistance gene.

FIG. 6 is a schematic showing assaying of TF-specific addresses (barcodes).

FIGs. 7A-7C include a series of t-SNE projections showing single cell RNA-seq results with or without amplifying the TF addresses (barcodes). FIG. 7A is a t-SNE projection showing single cell RNA-seq results for combinatorial TF assaying without reading out TF addresses. Single dots represent single cells. FIG. 7A shows that when TF addresses were not read out, many overexpressed TFs were not easily detected. . FIG. 7B is a t-SNE projection of single cell RNA-seq data for combinatorial TF assaying with address readout. FIG. 7B shows that a large number of cells in the top left cluster with TF

overexpression was immediately detected when the TF addresses were read out. FIG. 7C is a t-SNE projection of a combination of differentiation and pluripotent cells by endogenous OCT4 expression. FIG. 7C shows that the rightmost cluster of single cells were likely hiPSCs that did not express TFs because they remained pluripotent as observed by the high OCT4 expression.

FIGs. 8A-8E is a series of schematics depicting assembly of multiple transcription factors into one barcoded piggyB AC^™ vector using programmable Aarl restriction enzyme sites. FIG. 8A is a schematic showing pDNOR shuttling vectors, each encoding one transcription factor ( i.e ., transcription factor 1 (TF1), transcription factor 2 (TF2) or transcription factor 3 (TF3)). FIG. 8B is a schematic showing PCR to add on a linker (squares) and AArl restriction sites (stars). FIG. 8C is a schematic showing digestion of the PCR products and the piggyB AC^™ vector. FIG. 8D is a schematic showing ligation of the PCR products into the piggyB AC^™ vector. FIG. 8E is a schematic showing a final piggyB AC^™ vector encoding multiple transcription factors and a combination- specific barcode (address). Additional elements of the vector are labeled as in FIG. 5. DETAILED DESCRIPTION

The technology described herein enables sensitive detection of combinatorial transcription factor expression in many (e.g., hundreds to thousands of) individual cells and mapping of transcription factor expression to a particular cell and/or cell type. The present disclosure is based, at least in part, on unexpected results demonstrating that a barcoded transposon vector, compatible with droplet-based single cell RNA sequencing, can be used in mammalian stem cells as an expression vector to identify, with high efficiency and accuracy, specific combinations of transcriptions factors that mediate cell type conversion processes.

Cells may be reprogrammed to produce a variety of cell types. For example, stem cells may be obtained from a patient, converted into a cell type that is suitable to improve a particular condition and reinfused into the patient. Such use of autologous cells minimizes the risk of an adverse immune response and enables personalized treatment. In order to promote cell type conversion (e.g., stem cell differentiation), however, it is necessary to identify a combination of transcription factors capable of cellular reprogramming. Existing methods, such as single cell RNA sequencing often cannot capture transcripts expressed from exogenous nucleic acids (i.e., nucleic acids introduced into cells) with high sensitivity. For example, single cell RNA sequencing may only identify a fraction of such transcripts. Thus, it is often necessary to filter out cells in which such transcripts cannot be detected and rely on a few cells with robust signal. Alternatively, transcriptomes from multiple cells can be pooled to increase detection, but such methods cannot be used in large-scale analyses to map particular transcription factor combinations with a specific transcriptome. The technology provided herein address the foregoing challenges.

The vectors of the present disclosure, in some embodiments, comprises a cargo element with (i) a promoter operably linked to a nucleotide sequence encoding a transcription factor and a barcode, and (ii) a terminator sequence, wherein the barcode, which uniquely identifies the transcription factor, is located within 100 nucleotides (e.g., within 95, within 90, within 80, within 75, within 70, within 65, within 60, within 55, within 50, within 45, within 40, within 35, within 30, within 25, within 20, within 15, within 10 or within 5 nucleotides) of the 5' end of the terminator sequence. In some embodiments, the cargo element is flanked by terminal repeat sequences (e.g., inverted terminal repeat sequences or long terminal repeat sequences) recognized by a cognate transposase. In some embodiments, the vector is a transposon vector (comprising a transposon). Transposons

Transposons or transposable elements are mobile genetic elements that can insert into a nucleic acid. Structurally, a transposon comprises a cargo element ( i.e ., a nucleic acid sequence to be moved). Naturally-occurring transposons can move from one genomic locus to another. Transposons may comprise terminal repeat sequences (or terminal repeats), which are repetitive sequences flanking (on both ends of) a cargo sequences.

There are at least two classes of transposons. Class I transposons (also known as retrotransposons) are first transcribed into RNA, converted into DNA by reverse transcriptase and the resulting DNA is integrated into the genome at target sites. Class I transposons may be further classified into at least two subtypes. One subtype of class I transposons have long terminal repeats (repetitive sequences) flanking a cargo sequence while another subtype does not have long terminal repeat sequences. In contrast, class II transposons use a“cut and paste” mechanism, whereby the transposon is excised and inserted into a new location without an RNA intermediate. Class II transposons typically comprise a 5’ inverted terminal repeat and a 3’ inverted terminal repeat sequence flanking a cargo element. Inverted terminal repeats within a transposon are typically reverse complements of one another.

Transposases are enzymes that recognize the terminal repeats ( e.g ., long terminal repeats or inverted terminal repeats) on the ends of a transposon and catalyze the relocation of the transposon. For example, transposases can bind to terminal repeat sequences, excise the transposon carrying a cargo element, and insert the excised transposon into another nucleic acid.

Numerous transposon systems have been adapted for use in genetic engineering. For example, the piggyB AC^™ transposon system was originally identified in the cabbage looper moth Trichoplusia ni (Fraser et al, J Virol. 1983;47:287-300; Cary et al, Virology.

1989;161:8-17). PiggyB AC^™ transposases may bind to inverted terminal repeats comprising a TTAA sequence and transfer transposons into target sites comprising a TTAA sequence.

An exemplary sequence encoding piggyBac™ transposase is described in GenBank accession number: EF587698. Other piggyB AC^™ transposase sequences include piggyB AC^™ variants (e.g., hyperactive piggyB AC^™ transposase variants described in US 20130160152). The Sleeping Beauty transposon system was reconstructed from ancient fish genomes and are similar to the Tcl/mariner superfamily of transposons (Ivies et al, Cell. 1997 Nov

14;91(4):501-10). Sleeping Beauty transposases may insert transposons at target sites comprising a TA dinucleotide. Exemplary Sleeping Beauty transposases include transposases with wildtype sequence and variants thereof ( e.g ., SB11, SB100 and SB100X). See, e.g., Ivies et al., Cell. 1997 Nov 14;91(4):501-10 and Hou et al., Cancer Biol Ther.

2015; 16(1):8-16.

It should be understood that the present disclosure encompasses the use of any one or more of the transposases described herein as well as transposases that share a certain degree of sequence identity with the reference protein. The term“identity” refers to a relationship between the sequences of two or more polypeptides or polynucleotides, as determined by comparing the sequences. Identity measures the percent of identical matches between the smaller of two or more sequences with gap alignments (if any) addressed by a particular mathematical model or computer program (e.g.,“algorithms”). Identity of related molecules can be readily calculated by known methods. “Percent (%) identity” as it applies to amino acid or nucleic acid sequences is defined as the percentage of residues (amino acid residues or nucleic acid residues) in the candidate amino acid or nucleic acid sequence that are identical with the residues in the amino acid sequence or nucleic acid sequence of a second sequence after aligning the sequences and introducing gaps, if necessary, to achieve the maximum percent identity. Identity depends on a calculation of percent identity but may differ in value due to gaps and penalties introduced in the calculation. Variants of a particular sequence may have at least 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% but less than 100% sequence identity to that particular reference sequence, as determined by sequence alignment programs and parameters described herein and known to those skilled in the art.

The transposases described herein may contain one or more amino acid substitutions relative to its wild-type counterpart. Variants can be prepared according to methods for altering polypeptide sequence known to one of ordinary skill in the art such as are found in references which compile such methods, e.g. Molecular Cloning: A Laboratory Manual, J. Sambrook, et ah, eds., Second Edition, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York, 1989, or Current Protocols in Molecular Biology, F.M. Ausubel, et ah, eds., John Wiley & Sons, Inc., New York. Conservative substitutions of amino acids include substitutions made amongst amino acids within the following groups: (a) M, I, L, V; (b) F, Y, W; (c) K, R, H; (d) A, G; (e) S, T; (f) Q, N; and (g) E, D.

The comparison of sequences and determination of percent identity between two sequences can be accomplished using a mathematical algorithm. Techniques for determining identity are codified in publicly available computer programs. Exemplary computer software to determine homology between two sequences include, but are not limited to, GCG program package (Devereux, J. et al. Nucleic Acids Research, 12(1): 387, 1984), the BLAST suite (Altschul, S. F. et al. Nucleic Acids Res. 25: 3389, 1997), and FASTA (Altschul, S. F. et al. J. Molec. Biol. 215: 403, 1990). Other techniques include: the Smith- Waterman algorithm (Smith, T.F. et al. J. Mol. Biol. 147: 195, 1981; the Needleman-Wunsch algorithm

(Needleman, S.B. et al. J. Mol. Biol. 48: 443, 1970; and the Fast Optimal Global Sequence Alignment Algorithm (FOGSAA) (Chakraborty, A. et al. Sci Rep.3: 1746, 2013).

Nucleic acids and Cargo Elements

The nucleic acids of the present disclosure encode at least one transposon with a cargo element comprising a promoter operably linked to a nucleotide sequence encoding a transcription factor and a barcode that is located within 100 nucleotides 5’ upstream of a terminator sequence. In some embodiments, the nucleic acid comprises terminal repeat sequences (e.g., inverted terminal repeats or long terminal repeats) that are recognized by a transposase (e.g., piggyBAC^™transposase). A nucleic acid, generally, is at least two nucleotides covalently linked together, and in some instances, may contain phosphodiester bonds (e.g., a phosphodiester“backbone”). A nucleic acid is considered“engineered” if it does not occur in nature. As used herein, a population of nucleic acids indicates more than one nucleic acid (e.g., at least 2, at least 5, at least 10, at least 20, at least 30, at least 40, at least 50, at least 60, at least 70, at least 80, at least 90, at least 100, at least 200, at least 300, at least 400, at least 500, at least 600, at least 700, at least 800, at least 900, at least 1000, at least 1500, at least 2,000, at least 5,000 or at least 10,000 nucleic acids).

A terminator sequence is a nucleic acid sequence that mediates termination of transcription. Any terminator sequence known in the art or variants thereof may be used. For example, the terminator sequence may be a eukaryotic (e.g., mammalian) terminator sequence. Exemplary mammalian terminator sequences include SV40 terminator sequences, hGH terminator sequences, BGH terminator sequences and rbGlob terminator sequences. In some embodiments, a terminator sequence comprises a AAUAAA sequence motif.

Barcodes

Each barcode is located within 100 nucleotides (e.g., within 95, within 90, within 80, within 75, within 70, within 65, within 60, within 55, within 50, within 45, within 40, within 35, within 30, within 25, within 20, within 15, within 10 or within 5 nucleotides) of a terminator sequence and is located 5’ upstream of the terminator sequence. In some embodiments, the distance between the barcode and the 5’ end of the terminator sequence permits detection of at least 50% (e.g., at least 60%, at least 70%, at least 80%, at least 90% or at least 99%) of cells comprising the barcode ( e.g ., as detected by single cell RNA sequencing).

A barcode may be 1-100 nucleotides in length (e.g., 1-10 nucleotides in length, 10-20 nucleotides in length, 20-30 nucleotides in length, 30-40 nucleotides in length, 40-50 nucleotides in length, 50-60 nucleotides in length, 60-70 nucleotides in length, 70-80 nucleotides in length or 90-100 nucleotides in length). A barcode may be 20-100 nucleotides in length. Any method known in the art may be used to generate the barcodes. See, e.g., Smith et al, Nucleic Acids Res. 2010 Jul; 38(13): el42 and the Examples section below.

The sequence of a particular barcode may have certain characteristics. In some embodiments, a barcode has 25-65% GC content. In some embodiments, a barcode a homopolymer sequence of up to four of the same base. In some embodiments, all the barcodes within a population of nucleic acids are unique. In some embodiments, each barcode within a population of nucleic acids has a Hamming distance of greater than or equal to 6. Any algorithm known in the art for calculating the Hamming distance may be used. Exemplary barcodes include, but are not limited to, those provided in Table 1. Other barcodes sequences may be generated and used as provided herein.

Table 1. Exemplary Barcode Sequences.

A barcode may uniquely identify at least one transcription factor ( e.g ., at least 2, at least 3, at least 4, at least 5, at least 10, at least 10, at least 20, at least 50 or at least 100 transcription factors). For example, one barcode sequence may be associated with one transcription factor among a particular population of transcription factors such that the sequence of the one barcode correlates with only that one transcription factor among the particular population of transcription factors. In some embodiments, a barcode uniquely identifies a combination of transcription factors (i.e., more than one transcription factor).

Any transcription factor from any species (e.g., human, mouse, dog, cat, pig or bird) known in the art and variants thereof may be used. The sequences of exemplary transcription factors may be obtained from the National Center for Biotechnology Information (NCBI) GenBank database. Exemplary transcription factors include, but are not limited to, those provided in Table 2. In some embodiments, the transcription factors direct stem cell differentiation or other cell type conversion process.

Table 2. Exemplary Transcription Factors.

Multicistronic Vectors

In some embodiments, a cargo element of the present disclosure comprises a promoter operably linked to a nucleotide sequence (e.g., open reading frame (ORF)) encoding at least one transcription factor (e.g., at least 2, at least 3, at least 4, at least 5, at least 10, at least 10, at least 20, at least 50 or at least 100 transcription factors) and a barcode located within 100 nucleotides (e.g., within 50 nucleotides) 5’ upstream of a terminator. For example, for a cargo element encoding two or more transcription factors, each transcription factor may be operably linked to a different promoter or the same promoter. In some embodiments, a promoter is operably linked to at least two transcription factor nucleotide sequences (e.g., ORFs), wherein each transcription factor nucleotide sequence is separated by a separation sequence.

As used herein, a separation sequence promotes the formation of two separate amino acid sequences from one RNA transcript. For example, a separation sequence may encode a self-cleaving peptide. Exemplary self-cleaving peptides include 2A peptides (e.g., T2A,

P2A, E2A and F2A). The sequence of 2A peptides and variants thereof are known in the art. An exemplary sequence for T2A is EGRGSLLTCGDVEENPGP (SEQ ID NO: 20), an exemplary sequence for P2A is ATNFS LLKQAGD VEENPGP (SEQ ID NO: 21), an exemplary sequence for E2A is QCTN Y ALLKL AGD VES NPGP (SEQ ID NO: 22) and an exemplary sequence for F2A is VKQTLNFDLLKLAGDVESNPGP (SEQ ID NO: 23). In some embodiments, a separation sequence is an internal ribosomal entry site elements (IRES) sequence.

Epitope Tags

The nucleotide sequence encoding the transcription factor and the barcode may further encode an epitope tag that enables detection of transcription factor expression.

Exemplary epitope tags include c-Mc, V5, GFP, GST, FLAG and hemagglutinin A (HA).

The epitope tag may be detected by assessing RNA or protein levels using any method known in the art (e.g., western blot, ELISA or reverse transcription polymerase chain reaction (RT-PCR)).

Selection Agents

The cargo elements of the present disclosure may further comprise a second promoter operably linked to a second nucleotide sequence encoding a selection marker and/or inducing agent in order to permit the selection of transcription factor-integrated cells and/or to control transcription. Selection markers include antibiotic resistance markers (e.g. , puromycin, hygromycin or blasticidin) and fluorescent proteins (e.g., RFP, BFP, or GFP). Exemplary inducing agents include alcohols, tetracyclines (e.g., reverse tetracycline-controlled transactivator protein), steroids (e.g., estrogen), and metals. A separation sequence may be located in between a nucleotide sequence encoding a selection marker and a nucleotide sequence encoding an inducing agent. In some embodiments, an inducing agent is capable of promoting transcription from the promoter operably linked to a nucleotide sequence encoding a transcription factor and a barcode that is within 100 nucleotides 5’ upstream of a terminator sequence.

Barrier insulator sequences known in the art may also be included in cargo elements to prevent chromatin silencing.

Promoters

A promoter control region of a nucleic acid is a sequence at which initiation and rate of transcription of the remainder of a nucleic acid sequence are controlled. A promoter may also contain sub-regions at which regulatory proteins and molecules may bind, such as RNA polymerase and other transcription factors. Promoters may be constitutive, inducible, activatable, repressible, tissue-specific or any combination thereof. A promoter drives expression or drives transcription of the nucleic acid sequence that it regulates. Herein, a promoter is considered to be“operably linked” when it is in a correct functional location and orientation in relation to a nucleic acid sequence it regulates to control (“drive”)

transcriptional initiation and/or expression of that sequence.

An inducible promoter is one that is characterized by initiating or enhancing transcriptional activity when in the presence of, influenced by or contacted by an inducing agent. An inducing agent may be endogenous or a normally exogenous condition, compound or protein that contacts an engineered nucleic acid in such a way as to be active in inducing transcriptional activity from the inducible promoter.

Inducible promoters for use in accordance with the present disclosure include any inducible promoter described herein or known to one of ordinary skill in the art. Examples of inducible promoters include, without limitation, chemically/biochemically-regulated and physically-regulated promoters such as alcohol-regulated promoters, tetracycline-regulated promoters (e.g., anhydrotetracycline (aTc)-responsive promoters and other tetracycline responsive promoter systems, which include a tetracycline repressor protein (tetR), a tetracycline operator sequence (tetO) and a tetracycline transactivator fusion protein (tTA)), steroid-regulated promoters (e.g., promoters based on the rat glucocorticoid receptor, human estrogen receptor, moth ecdysone receptors, and promoters from the steroid/retinoid/thyroid 25 receptor superfamily), metal-regulated promoters (e.g., promoters derived from

metallothionein (proteins that bind and sequester metal ions) genes from yeast, mouse and human), pathogenesis-regulated promoters (e.g., induced by salicylic acid, ethylene or benzothiadiazole (BTH)), temperature/heat-inducible promoters (e.g., heat shock promoters), and light-regulated promoters (e.g., light responsive promoters from plant cells). In some embodiments, a nucleic acid comprises at least one inducible promoter ( e.g ., at least 2, at least 3, at least 4, at least 5, at least 6, at least, 8, or at least 10 inducible promoters). In some embodiments, a nucleic acid comprises an inducible promoter operably linked to a nucleotide sequence encoding a transcription factor and a barcode that is located within 100 nucleotides 5’ upstream of a terminator sequence. In some embodiments, a nucleic acid comprises an inducible promoter operably linked to a nucleotide sequence encoding a selection marker and/or inducing agent.

A constitutive promoter is capable of initiating or enhancing transcriptional activity regardless of the presence or absence of an inducible agent. For example, a promoter may be a constitutive promoter suitable for expression within mammalian cells. Exemplary constitutive promoters include, but at are not limited to, EFla, CMV, SV40, PGK1 and Ubc. In some embodiments, a nucleic acid comprises at least one constitutive promoter (e.g., at least 2, at least 3, at least 4, at least 5, at least 6, at least, 8, or at least 10 inducible promoters). In some embodiments, a nucleic acid comprises a constitutive promoter operably linked to a sequence encoding a selection marker or an inducing agent. In some embodiments, a nucleic acid comprises a constitutive promoter operably linked to a sequence encoding a transcription factor and a barcode that is located within 100 nucleotides 5’ upstream of a terminator sequence.

Cloning Vectors

Some aspects of the present disclosure also provide cloning vectors for use, for example, in producing any of the nucleic acids described herein. In some embodiments, a cloning vector comprises a transposon in which the cargo element in the transposon comprises a promoter operably linked to a multiple cloning site and to a barcode that is located within 100 nucleotides (e.g., within 95, within 90, within 85, within 80, within 75, within 70, within 65, within 60, within 55, within 50, within 45, within 40, within 35, within 30, within 25, within 20, within 15, within 10 or within 5 nucleotides) 5’ upstream of a terminator sequence. In some embodiments, the vector further comprises terminal repeats (e.g., inverted terminal repeats or long terminal repeats). The multiple cloning site may comprise at least two restriction enzyme recognition sites (e.g., Aarl restriction enzyme sites). The cloning vector may be a piggyBAC^™ cloning vector (i.e., a cloning vector with inverted piggyB AC^™ inverted terminal repeats).

Any of the nucleic acids and cloning vectors herein may be produced using any recombinant technique known in the art. In some embodiments, programmable restriction enzyme sites ( e.g ., Aarl restriction enzyme sites) may be used to assemble a nucleic acid of the present disclosure. See, e.g., the Examples section below. In some embodiments, restriction sites recognized by different restriction enzymes are used to assemble a nucleic acid sequence encoding a combination of transcription factors in a predetermined order.

Methods and Cells

Provided herein are methods for identifying a combination of transcription factors capable of mediating cell differentiation. In some embodiments, the methods comprise contacting cells with a population of any of the nucleic acids described herein, identifying differentiated cells (e.g., using single cell RNA sequencing) and detecting one or more barcodes in the differentiated cells to identify the combination of transcription factors capable of inducing cell differentiation. In some embodiments, the cells further comprise a transposase.

Any of the nucleic acids may be introduced into cells (e.g., stem cells) using conventional methods (e.g., nucleofection) to express one or more transcription factors that may be identified by a barcode. A transposase may be delivered into cells using a separate expression vector encoding the transposase or the nucleic acids described herein may further encode a transposase. In some embodiments, a population of nucleic acids are introduced (e.g., by nucleofection) into cells such that cells receive at least one copy of any of the cargo elements described herein (e.g., at least 2, at least 5, at least 10, at least 20, at least 30, at least 40, at least 50, at least 60, at least 70, at least 80, at least 90, at least 100, at least 200, at least 300, at least 400, at least 500, at least 600, at least 700, at least 800, at least 900, at least 1000, at least 1500, at least 2,000, at least 5,000 or at least 10,000 cargo elements). For example, parameters including cell number, nucleic acid concentration, and transposase concentration may be altered for this purpose. See, e.g., the nucleofection conditions in the Examples section below. Cells may be further cultured in the presence of a selection agent (e.g., antibiotic) for at least one day (e.g., at least 2 days, at least 3 days, at least 3 days at least 5 days, at least 10 days or at least 14 days) to select for cells with genomic integration of a cargo element encoding a transcription factor. In some embodiments, cells are cultured in the presence of an inducing agent for at least one day (e.g., at least 2 days, at least 3 days, at least 3 days at least 5 days, at least 10 days or at least 14 days) to induce expression of one or more transcription factors.

Cell types may be characterized by their gene expression profiles. Therefore, gene expression at the RNA or protein level may be used to identify a particular cell type (e.g., to identify differentiated cells). For example, any single cell RNA sequencing technique known in the art ( e.g ., droplet-based single cell RNA sequencing) may be used to generate a gene expression profile of single cells and the transcriptome of a single cell may be mapped to a transcriptome of a known cell type. See, e.g., Klein et al, Cell. 2015 May 21 ; 161(5): 1187- 1201. As an example, t-distributed stochastic neighbor embedded (t-SNE) may be used as a computational method to visualize single cell gene expression data. See, e.g., Maaten, J. Mach. Learn. Res. 2008; 9:2579-2605 for a description of t-SNE. The transcriptome may be used qualitatively or quantitatively. In some embodiments, single cell RNA sequencing is used to generate a gene expression profile (e.g., by assessing RNA expression of at least one gene) from a cell carrying any of the nucleic acids encoding a transcription factor of the present disclosure. This gene expression profile may then be compared with the gene expression profile of one or more control cells. Suitable control cells include cells that have not been contacted with a nucleic acid of the present disclosure. Control cells may be cells whose gene expression profile is associated with a particular cell type. Such comparison of gene expression profiles between single cells and cells of a known cell type may be used to identify single cells that are differentiated cells. Classification of transcription factor-induced lineages has previously been described. See e.g., International Patent Application Publication Number WO 2018/049382, which was published on March 15, 2018. Additional methods for distinguishing between differentiated cells and non-differentiated cells include fluorescence activated cell sorting based on surface marker expression (e.g., expression of at least one lineage- specific cell surface antigen) and proteome analysis.

The barcode associated with a transcription or a combination of transcription factors may be detected using any sequencing method known in the art. In some embodiments, at least one barcode (e.g., at least 2, at least 5, at least 10, at least 20, at least 30, at least 40, at least 50, at least 60, at least 70, at least 80, at least 90, at least 100, at least 200, at least 300, at least 400, at least 500, at least 600, at least 700, at least 800, at least 900, at least 1000, at least 1500, at least 2,000, at least 5,000 or at least 10,000 barcodes) within a differentiated cell is detected. In some embodiments, RNA single cell sequencing is used to detect at least one barcode in a differentiated cell to identify at least one transcription factor.

In some embodiments, the methods described herein identify transcription factors capable of mediating stem cell differentiation. As used herein, a stem cell may be a pluripotent stem cell. Pluripotent stem cells are cells that have the capacity to self-renew by dividing, and to develop into the three primary germ cell layers of the early embryo, and therefore into all cells of the adult body, but not extra-embryonic tissues such as the placenta. Embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) are pluripotent stem cells. ESCs are derived from the undifferentiated inner mass cells of a human embryo and are able to differentiate into all derivatives of the three primary germ layers: ectoderm, endoderm and mesoderm. iPCSs can be generated directly from adult cells (Takahashi, K; Yamanaka, S. Cell l26(4):663-76, 2006). In some embodiments, a pluripotent stem cell is an ESC. In some embodiments, a pluripotent cell is an iPSC. In some embodiments, a pluripotent stem cell is a human ESC. In some embodiments, a pluripotent cell is an iPSC. In some embodiments, a pluripotent cell is a human iPSC. In some embodiments, a

differentiated stem cell is a stem cell that has lost pluripotency.

A preparation of pluripotent stem cells (e.g., expressing the transcription factor combination as provided herein) may be cultured under standard stem cell culture conditions. For example, the pluripotent stem cells may be cultured in any commercially-available feeder-free maintenance medium for human ESCs and iPSCs, such as mTeSR™l media. In some embodiments, the pluripotent stem cells are cultured in commercially-available stem cell media without added nutrients or growth factors.

Differentiated cells may be separated from stem cells by gene expression (e.g., RNA or protein expression) as described above. For example, expression of markers, including TRA-l-60, OCT4 or a combination thereof, may be used to distinguish pluripotent cells from differentiated cells. See, e.g., the Examples section below and International Patent

Application Publication Number WO 2018/049382, which was published on March 15, 2018.

Aspects of the present disclosure also provide a cell, including a population of cells, comprising any of the nucleic acids described herein. In some embodiments, the cell further comprise a transposase.

EXAMPLES

Example 1: Development of a barcoded piggyBAC^™ transcription factor expression vector suitable for single-cell sequencing.

To first pilot a combinatorial transcription factor (TF) assay using single cell RNA- sequencing, a piggyBAC^™ expression vector without a barcode was used (FIG. 1A). The piggyBAC^™ vector containing TFs was nucleofected into human induced pluripotent stem cells (hiPSCs), puromycin selection was performed to isolate cells that have stably integrated the TFs, and these cells were expanded and TF overexpression was induced by doxycycline addition for four days (FIG. 1B). Emulsion-droplet-based RNA sequencing, which captures single cells within aqueous droplets containing a barcoded gel with a unique cell barcode (Klein et al, Cell 161, 1187-1201 (2015); Macosko et al, Cell 161, 1202-1214 (2015)), was performed. Libraries were prepared and 401 single cells were sequenced. The overexpressed TFs were detected and identified in only 57 of 401 cells (14.2%, FIG. 1C). Furthermore, for cells where any signal of the overexpressed TF was detected, the TF ORF could not be identified because too few bases were sequenced, likely due to fragmentation of upstream sequence (FIG. 1D). Thus, these results demonstrate two issues: first, the overexpressed TF could not be detected in a sensitive manner in most cells and second, of the TFs detected, it was not possible to reliably identify it.

To improve sensitivity of detection and identification of the overexpressed TF, improvements in the reverse transcription step were tested. Single cell RNA-seq was performed on hiPSCs without TF overexpression and expression of an endogenous TF,

OCT4, was assessed. This pluripotency TF is expressed at low levels in cells, yet robust expression of this TF was detected in virtually all cells without modification to the protocol (FIG. 2). This suggested that adaptations in reverse transcription or library preparation may not yield large gains in signal.

To test whether improvements to the expression level of the overexpressed TF itself boost detection levels, the RNA-seq experiments were analyzed to determine the level of overexpression of the TFs. Robust expression of the overexpressed TF was observed, with levels up to an increase of 30,000-fold compared to non-induced controls (FIG. 3). Due to the high level of overexpression, it was concluded that it is not advantageous to further maximize overexpression, as this may already be at maximal levels and further increases could affect cell physiology, for instance by reducing available ribosomes for the production of essential proteins.

Based on the observations that single cell RNA sequencing could detect endogenous, TF expression at low levels and exogenous overexpression at high levels, a new vector was rationally designed to enable detection and identification of the TFs overexpressed at high levels (FIGs. 4A-4E).

First, the location of modifications that would minimize impact to the function of the vector, while being compatible with single cell RNA sequencing, were considered. This was viewed in light of the library preparation process (FIG. 4A). Modifications in sequence region 1 may cause changes in TF function. Modifications in sequence region 2 may inhibit cloning of the TF into the vector. Modifications in sequence region 3 may be possible. Modifications in sequence region 4 may adversely affect transcriptional termination. For these reasons, engineering improvements were focused on sequence region 3.

Sequence region 3 contains 143 base pairs. This region was further analyzed to determine areas that were amenable to modification (FIG. 4B). Modifications to sequence region 5 used a primer upstream for PCR. Such a primer would bind AttB2. However, this region had high sequence identity with another region on the vector, AttBl (FIG. 4C). This prevented specific primer binding. Next, sequence region 6 was considered. The upstream primer would bind the V5 tag, which had previously been used successfully for PCR.

However, based on the experiments described in FIG. 1, these bases were far away from the transcriptional terminator, and hence the capture site near the gel. This meant this area could not be sequenced due to fragmentation. Therefore, sequence region 7 was considered, which was closer to the capture site near the gel. However, repetitive sequences (FIG. 4D) and sequences with high homopolymer content (FIG.4E) were found. For these reasons, sequence region 8 was determined to be ideal for modification. A schematic of a barcoded

piggyB AC^™ vector for transcription factor expression is provided in FIG. 5. The barcode ( i.e address) is located upstream of the first transcription terminator sequence (indicated by a bolded T in FIG. 5). This transcription factor expression vector enables targeted detection of the barcode, which is directly linked to the transcription factor.

With a suitable sequence region identified, TF-specific DNA addresses (barcodes) were cloned into sequence region 8 of the piggyB AC^™ vector that could be recovered by single cell RNA sequencing. 1,921 addresses were cloned and assayed for additional features that would maximize the sensitivity of detection, to arrive at 858 high-quality addresses (FIG. 6). First, addresses outside a 25-65% GC content were rejected, resulting in 1,594 acceptable addresses. Then, addresses with homopolymers of greater than four of the same base were removed, resulting 1,239 addresses. Additionally, addresses where more than one base was ambiguous were removed, yielding 1,151 addresses. Another set of addresses were rejected due to improper cloning and 1,016 addresses passed. Finally, all addresses were compared to every other address to remove those that were similar, as defined by a Hamming distance of less than 6. This resulted in 858 acceptable addresses.

With this TF-addressable (TF-barcoded) piggyB AC^™ vector, detection of the overexpressed TF was tested by single cell RNA sequencing. A new population of hiPSCs was generated containing a combination of TFs expressed using this new, single-cell optimized piggyB AC^™ vector, and mixed it with a population of hiPSCs containing TFs expressed using the original piggyB AC^™ vector for comparison and with a population of hiPSCs that did not express TFs as a negative control. The combination of TFs used were neurogenin-3 (NGN3), NKX3.2 and ETV2 and each transcription factor was delivered on a separate barcoded piggyB AC^™ vector. Single cell RNA-seq with or without amplifying the TF addresses was performed. The three populations of cells could immediately be identified by single cell RNA sequencing, as three clusters appeared using t-SNE projection (FIGs.7A- 7C). When TF addresses were not read out, many overexpressed TFs were not easily detected (FIG.7A). In contrast, using the optimized detection by reading out the TF address, a large number of cells in the top left cluster with TF overexpression was immediately detected (FIG.7B). This was not seen in the other two clusters, as expected, due to the lack of these addresses or the lack of TFs. It was possible to infer that the rightmost cluster were hiPSCs that did not express TFs because they remained pluripotent as observed by the high OCT4 expression (FIG. 7C). Together, these results demonstrate an ability to simultaneously detect changes in the transcriptomic state of single cells as well as the overexpressed TFs that caused this change.

Methods

Cell culture

The PGP1 hiPSC line without genomically integrated Yamanaka factors was generated from fibroblasts (Coriell, GM23248) (72) using the CytoTune Sendai

Reprogramming Kit (Life Tech, A16517). They were adapted to feeder-free culture, verified for pluripotency by FACS, and karyotyped. Cell lines were verified by short tandem repeat (STR) profiling (Dana Farber Cancer Institute), regularly verified to be mycoplasma-free using PlasmoTest (InvivoGen, rep-ptl), and cultured between passages 8 and 40. hiPSCs were cultured in mTeSRl (STEMCELL Technologies, 05850) without antibiotics on tissue- culture-treated plates coated with Matrigel (Coming, 354277). hiPSCs were passaged using TrypLE Express (Life Technologies, 12604013) and seeded with IOmM Y-27632 ROCK inhibitor (Millipore, 688001) for one day. Cells were frozen in mFreSR (STEMCELL Technologies, 5854) using a CoolCell LX (Biocision, BCS-405) overnight at -80°C, then in vapor-phase liquid nitrogen for long-term storage.

Nucleofection of piggyBAC^™and generation of stable cell lines

The first piggyB AC^™ vector without a barcode, PBAN is a Gateway-compatible, doxycyc line-inducible, puromycin- selectable piggyB AC^™ vector. It was constructed from PB-TRE-dCas9-VPR (Addgene #63800). Individual pDONR-TFs were cloned into PBAN using LR Clonase II. 500,000 to 800,000 hiPSCs were nucleofected with PBAN-TF and Super piggyB AC^™ Transposase (SPB; System Biosciences, PB210PA-1) at a DNA ratio of 4:1 using Nucleofector P3 solution (Lonza, V4XP-3032). Nucleofected cells were transferred to a 6-well Matrigel-coated plate in mTeSRl with ROCK inhibitor. When cells reached 80% confluence, lpg/ml puromycin (Gibco, Al l 13803) was added. The next day, dead cells in suspension were washed away using PBS; if the remaining cells were sparse, ROCK inhibitor was added to prevent colony collapse. 500ng/mL doxycycline (Sigma) was used for induction.

Droplet-based single cell RNA-seq library preparation and analysis

Cells were dissociated, counted and resuspended in mTeSRl and captured with the droplet-based Chromium V2 single cell RNA-seq kit (lOx Genomics, 120237) using manufacturer’s protocols. Libraries were sequenced on an Illumina MiSeq or NextSeq, and processed using lOx Genomics’ CellRanger pipeline to generate gene-cell barcode-matrices. To readout TF addresses, lOng of the sample after whole-transcriptome amplification was used for PCR using universal address primers to amplify the addresses with Illumina sequencing adaptors.

Forward primer:

5' -AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTC (SEQ ID NO: 24)

Reverse primers (unique to each sample):

5' -

CAAGCAGAAGACGGCATACGAGATatgctgtcGTGACTGGAGTTCAGACGTGTGCTCTTCCGATCTCCAAGCACC TGCTACATAGC (SEQ ID NO: 25)

5' -

CAAGCAGAAGACGGCATACGAGATtgtacaaaGTGACTGGAGTTCAGACGTGTGCTCTTCCGATCTCCAAGCACC TGCTACATAGC (SEQ ID NO: 26)

5' -

CAAGCAGAAGACGGCATACGAGATcacggcctGTGACTGGAGTTCAGACGTGTGCTCTTCCGATCTCCAAGCACC TGCTACATAGC (SEQ ID NO: 27)

5' -

CAAGCAGAAGACGGCATACGAGATgcatatggGTGACTGGAGTTCAGACGTGTGCTCTTCCGATCTCCAAGCACC TGCTACATAGC (SEQ ID NO: 28)

5' -

CAAGCAGAAGACGGCATACGAGATtactcgccGTGACTGGAGTTCAGACGTGTGCTCTTCCGATCTCCAAGCACC TGCTACATAGC (SEQ ID NO: 29)

5' -

CAAGCAGAAGACGGCATACGAGATatagaagtGTGACTGGAGTTCAGACGTGTGCTCTTCCGATCTCCAAGCACC TGCTACATAGC (SEQ ID NO: 30)

Amplified addresses were sequenced on an Illumina MiSeq. The sequencing data was processing using custom perl scripts that extracted the TF addresses belonging to each cell to assign counts. Single cell sequencing data was visualized in Geneious as raw sequencing reads, or in R as t-SNE plots.

Comparison with population RNA sequencing: library preparation

600m1 TRIzol (Life Technologies, 15596-018) was added directly to cells, which were then incubated for 3 minutes and used for RNA extraction using Direct-zol RNA MiniPrep (Zymo Research, R2050). At least three replicates of control cells (without doxycycline) were processed in parallel in each set of library preps. RNA was quantified using Qubit RNA HS Kit (Molecular Probes, Q32852) and RNA integrity was confirmed by the presence of intact 18S and 28S bands on a 1% E-Gel EX. lpg RNA was used for Poly(A) isolation using the NEBNext Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, E7490L) and the NEBNext Ultra Directional RNA Library Prep Kit for Illumina (New England Biolabs, E7420L). To prevent library over-amplification, one-fifth of the PCR reaction was amplified by quantitative PCR using SYBR Gold Nucleic Acid Statin on a Roche Lightcycler 480. The remaining reaction was amplified using the number of cycles needed to reach mid-log amplification. Library size was visualized on a 1% E-Gel EX, and quantified using KAPA Library Quantification Kit as described before.

Analysis of population RNA sequencing data.

A STAR human transcriptome reference index was generated using Gencode

GROG 8.primary :

(ftp://ftp.sanger.ac.uk/pub/gencode/Gencode_human/release_25/GRCh38.primary_assembly. genome.fa.gz) as the genome sequence and Gencode v25 transcript annotations

(ftp://ftp.sanger.ac.Uk/pub/gencode/Gencode_human/release_25/gencode.v25.annotation.gtf.g z). RNA-seq reads were aligned on four codes each with l2Gb memory using the command: STAR -quanode GeneCounts.

Gene counts per sample were merged into a master table and analyzed in R version 3.2.2. Differential expression analysis was performed using DESeq 2 (73), comparing each batch to its no-doxycycline control separately. FASTQ files will be available on NCBI GEO.

Construction of piggyBAC^™ vector for TF addressable readout using single cell

RNA

Addresses were synthesized as primers (Integrated DNA Technologies) and PCR using HiFi HotStart (KAPA Biosystems) was used to construct double stranded DNA fragments. These fragments were cloned into the first generation piggyBAC^™ PB AN vector described above upstream of BGH transcriptional terminator. Single colonies were sequenced and assayed for acceptable addresses by Sanger sequencing, and re-arrayed into individually addressable 96-well plates. Specific TFs were Gateway cloned into these individually addressed piggyBAC^™ vectors using LR clonase (Invitrogen), and used to create stable hiPSC lines.

Example 2: A barcoded piggyBAC^™ vector encoding multiple transcription factors.

FIGs. 8A-8E show steps for cloning of a barcoded piggyBAC^™ vector encoding multiple transcription factors. PDNOR shuttle vectors with an open reading frame encoding with each of the transcription factors (FIG. 8A) may be used. Polymerase chain reaction may be used to add a linker ( e.g ., encoding 2A self-cleavage peptide, IRES, etc.) between each of the open reading frames and to add Aarl restriction sites flanking each open reading frame (FIG. 8B). The PCR products and the piggyBAC^™ vector may be digested with the Aarl restriction enzyme (FIG. 8C) to generate programmable overhangs. The digested PCR products and vector can then be ligated together (FIG. 8D) to produce the final barcoded vector encoding multiple transcription factors (FIG. 8E).

All references, patents and patent applications disclosed herein are incorporated by reference with respect to the subject matter for which each is cited, which in some cases may encompass the entirety of the document.

The indefinite articles“a” and“an,” as used herein in the specification and in the claims, unless clearly indicated to the contrary, should be understood to mean“at least one.”

It should also be understood that, unless clearly indicated to the contrary, in any methods claimed herein that include more than one step or act, the order of the steps or acts of the method is not necessarily limited to the order in which the steps or acts of the method are recited.

In the claims, as well as in the specification above, all transitional phrases such as “comprising,”“including,”“carrying,”“having,”“containing,”“involving,”“holding,” “composed of,” and the like are to be understood to be open-ended, i.e., to mean including but not limited to. Only the transitional phrases“consisting of’ and“consisting essentially of’ shall be closed or semi-closed transitional phrases, respectively, as set forth in the United States Patent Office Manual of Patent Examining Procedures, Section 2111.03.

The terms“about” and“substantially” preceding a numerical value mean ±10% of the recited numerical value.

Where a range of values is provided, each value between the upper and lower ends of the range are specifically contemplated and described herein.

Claims

CLAIMS What is claimed is:

1. A method of identifying at least one transcription factor, comprising:

(a) contacting cells that comprise a transposase with a population of nucleic acids, wherein each nucleic acid comprises a cargo element flanked by terminal repeat sequences that are recognized by the transposase,

wherein each cargo element comprises

(i) a first promoter operably linked to a first nucleotide sequence encoding a transcription factor and a barcode, and

(ii) a terminator having a 5' end,

wherein the barcode uniquely identifies the transcription factor and is located within 100 nucleotides of the 5' end of the terminator;

(b) detecting differences in gene expression in the cells compared to control cells and identifying differentiated cells; and

(d) detecting one or more barcodes in the differentiated cells and identifying a transcription factor or a combination of transcription factors in the differentiated cells.

2. The method of claim 1, wherein the barcode is located within 50 nucleotides of the 5’ end of the terminator.

3. The method of claim 1 or 2, wherein the transposase is a piggyBAC^™ transposase.

4. The method of claim 1 or 2, wherein the terminal repeat sequences are long terminal repeat sequences.

5. The method of any one of claims 1-3, wherein the terminal repeat sequences are inverted terminal repeat sequences.

6. The method of any one of claims 1-5, wherein each nucleic acid further comprises a second promoter operably linked to a second nucleotide sequence encoding a selection marker.

7. The method of any one of claims 1-5, wherein each nucleic acid further comprises a second promoter operably linked to a second nucleotide sequence encoding an inducing agent.

8. The method of any one of claims 1-5, wherein each nucleic acid further comprises a second promoter operably linked to a second nucleotide sequence encoding a selection marker and an inducing agent.

9. The method of claim 8, wherein the inducing agent is separated from the selection marker by a separation sequence.

10. The method of claim 8, wherein the separation sequence is selected from the group consisting of a sequence encoding a self-cleaving peptide and an internal ribosome entry site.

11. The method of any one of claims 1-10, wherein the first promoter is an inducible promoter.

12. The method of any one of claims 1-10, wherein the first promoter is a constitutive promoter.

13. The method of any one of claims 6-12, wherein the second promoter is an inducible promoter.

14. The method of any one of claims 6-12, wherein the second promoter is a constitutive promoter.

15. The method of any one of claims 1-14, wherein the first nucleotide sequence further encodes an epitope tag.

16. The method of any one of claims 1-15, wherein the barcode has a length of 20-100 nucleotides.

17. The method of claim 16, wherein the barcode has a length of 20 nucleotides.

18. The method of any one of claims 1-17, wherein the control cells are not contacted with the plurality of nucleic acids.

19. The method of any one of claims 1-18 further comprising selecting cells with a selection agent.

20. The method of claim 19, wherein the selection agent is an antibiotic selected from the group consisting of puromycin, hygromycin, and blasticidin.

21. The method of any one of claims 7-20, further comprising contacting cells with an inducing agent.

22. The method of claim 21, wherein the inducing agent is selected from the group consisting of an alcohol, a tetracycline, a steroid, and a metal.

23. The method of claim 22, wherein tetracycline is the inducing agent.

24. The method of any one of claims 1-23, wherein the cargo element further comprises barrier insulator sequences.

25. The method of any one of claims 1-24, wherein the cell is a human cell.

26. The method of any one of claims 1-25, wherein the cell is a stem cell, optionally an induced pluripotent stem cell.

27. The method of any one of claims 1-26, the detecting step (b) comprises using single cell RNA sequencing to detect differences in gene expression in the cells compared to control cells to identify differentiated cells.

28. The method of any one of claims 1-27, wherein the first nucleotide sequence encodes at least two transcription factors.

29. The method of claim 28, wherein the first nucleotide sequence further encodes a separation sequence between each transcription factor.

30. A population of nucleic acids, wherein each nucleic acid comprises a cargo element flanked by terminal repeat sequences that are recognized by a transposase,

wherein the cargo element of each nucleic acid comprises:

(a) a first promoter operably linked to a first nucleotide sequence encoding at least one transcription factor and a barcode; and

(b) a terminator, and

wherein the barcode uniquely identifies the transcription factor and is located within 100 nucleotides of the 5’ end of the terminator.

31. The population of claim 30, wherein the barcode is located within 50 nucleotides of the 5’ end of the terminator.

32. The population of claim 30 or 31, wherein the transposase is a piggyBAC^™ transposase.

33. The population of claim 30 or 31, wherein the terminal repeat sequences are long terminal repeat sequences.

34. The population of any one of claims 30-32, wherein the terminal repeat sequences are inverted terminal repeat sequences.

35. The population of any one of claims 30-34, wherein each nucleic acid further comprises a second promoter operably linked to a second nucleotide sequence encoding a selection marker.

36. The population of any one of claims 30-34, wherein each nucleic acid further comprises a second promoter operably linked to a second nucleotide sequence encoding an inducing agent.

37. The population of any one of claims 30-34, wherein each nucleic acid further comprises a second promoter operably linked to a second nucleotide sequence encoding a selection marker and an inducing agent.

38. The population of claim 37, wherein the inducing agent is separated from the selection marker by a separation sequence.

39. The population of claim 38, wherein the separation sequence is selected from the group consisting of a sequence encoding a self-cleaving peptide and an internal ribosome entry site.

40. The population of any one of claims 30-39, wherein the first promoter is an inducible promoter.

41. The population of any one of claims 30-39, wherein the first promoter is a constitutive promoter.

42. The population of any one of claims 35-41, wherein the second promoter is an inducible promoter.

43. The population of any one of claims 35-41, wherein the second promoter is a constitutive promoter.

44. The population of any one of claims 30-43, wherein the first nucleotide sequence further encodes an epitope tag.

45. The population of any one of claims 30-44, wherein the barcode has a length of 20- 100 nucleotides.

46. The population of claim 45, wherein the barcode has a length of 20 nucleotides.

47. The population of any one of claims 30-46, wherein the cargo element further comprises barrier insulator sequences.

48. The population of any one of claims 30-47, wherein the first nucleotide sequence encodes at least two transcription factors.

49. The population of claim 48, wherein the first nucleotide sequence further encodes a separation sequence between each transcription factor.

50. A population of cells, wherein each cell comprises a transposase and a nucleic acid that comprises a cargo element flanked by terminal repeat sequences that are recognized by a transposase,

wherein the cargo element of each nucleic acid comprises:

(a) a first promoter operably linked to a first nucleotide sequence encoding at least one transcription factor and a barcode; and

(b) a terminator, and

wherein the barcode uniquely identifies the transcription factor and is located within 100 nucleotides of the 5’ end of the terminator.

51. The population of cells of claim 50, wherein the cell is a human cell.

52. The population of any one of claims 50-51, wherein the cell is a stem cell, optionally an induced pluripotent stem cell.

53. A cloning vector comprising a cargo element flanked by terminal repeat sequences that are capable of being recognized by a transposase,

wherein the cargo element of each nucleic acid comprises

(a) a first promoter operably linked to a multiple cloning site and a barcode, and

(b) a terminator, and

wherein the barcode is located within 100 nucleotides of the 5’ end of the terminator.

54. The cloning vector of claim 53, wherein the barcode is located within 50 nucleotides of the 5’ end of the terminator.

55. The cloning vector of claim 53 or 54, wherein the transposase is a piggyBAC^™ transposase.

56. The cloning vector of claim 53 or 54, wherein the terminal repeat sequences are long terminal repeat sequences.

57. The cloning vector of any one of claims 53-55, wherein the terminal repeat sequences are inverted terminal repeat sequences.

58. The cloning vector of any one of claims 53-57, wherein each nucleic acid further comprises a second promoter operably linked to a second nucleotide sequence encoding a selection marker.

59. The cloning vector of any one of claims 53-57, wherein each nucleic acid further comprises a second promoter operably linked to a second nucleotide sequence encoding an inducing agent.

60. The cloning vector of any one of claims 53-57, wherein each nucleic acid further comprises a second promoter operably linked to a second nucleotide sequence encoding a selection marker and an inducing agent.

61. The cloning vector of claim 60, wherein the inducing agent is separated from the selection marker by a separation sequence.

62. The cloning vector of claim 60, wherein the separation sequence is selected from the group consisting of a sequence encoding a self-cleaving peptide and an internal ribosome entry site.

63. The cloning vector of any one of claims 53-62, wherein the first promoter is an inducible promoter.

64. The cloning vector of any one of claims 53-62, wherein the first promoter is a constitutive promoter.

65. The cloning vector of any one of claims 53-64, wherein the second promoter is an inducible promoter.

66. The cloning vector of any one of claims 53-64, wherein the second promoter is a constitutive promoter.

67. The cloning vector of any one of claims 53-66, wherein the first nucleotide sequence further encodes an epitope tag.

68. The cloning vector of any one of claims 53-67, wherein the barcode has a length of 20-100 nucleotides.

69. The cloning vector of claim 68, wherein the barcode has a length of 20 nucleotides.

70. The cloning vector of any one of claims 53-69, wherein the control cells are not contacted with the plurality of nucleic acids.

71. The cloning vector of any one of claims 53-70, wherein the cargo element further comprises barrier insulator sequences.

72. The cloning vector of any one of claims 53-71, wherein the cell is a human cell.

73. The cloning vector of any one of claims 53-72, wherein the cell is a stem cell, optionally an induced pluripotent stem cell.

74. The cloning vector of any one of claims 53-73, wherein the first nucleotide sequence encodes at least two transcription factors.

75. The cloning vector of claim 74, wherein the first nucleotide sequence further encodes a separation sequence between each transcription factor.