1. Discovery

2. Structure

3. p38 MAPK & Mesenchymal Stem Cells

4. Embryo Development
    Tissue Derivation  Gene Control 

5. Expression in Adult Tissues

6. Rex1 Interactions with Other Transcription Factors
    Nanog  NOTCH  STAT3  Sox2  Oct3/4 

7. References

8. Further reading

Discovery

Rex1 was discovered by Hosler, BA et al. in 1989 when studying F9 murine teratocarcinoma stem cells. They found that these teratocarcinoma stem cells expressed high levels of Rex1, and that they resembled pluripotent stem cells of the inner cell mass (ICM).^[3] Hosler, BA et al. found that these teratocarcinoma stem cells, when in the presence of retinoic acid (RA), differentiated into nontumorigenic cells resembling extraembryonic endoderm of early mouse embryos.^[4] They were able to isolate the nucleotide sequence for Rex1 using differential hybridization of an F9 cell. They named it Rex1 for reduced expression 1 because there was a steady decline of its mRNA levels within 12 hours of the addition of RA.^[4]

Structure

Rex1 is a protein that in humans is encoded by the ZFP42 gene.^[5][6] The Rex1 protein is 310 amino acids long, and has four closely spaced zinc fingers at 188-212, 217-239, 245-269, and 275-299.^[3]

p38 MAPK & Mesenchymal Stem Cells

Rex1 has been found to be critically important in maintaining proliferative state in mesenchymal stem cells (MSC), while simultaneously preventing differentiation. Both umbilical cord blood MSC and adipose MSC express high levels of Rex1, while bone marrow MSC expressed low levels of Rex1. Proliferation rates are highly correlated with Rex1 expression levels, meaning high Rex1 expression is correlated with high levels of proliferation. The MSCs with weak Rex1 expression, have activated p38 MAPK and high expression levels of MKK3. Thus, Rex1 expression is inversely correlated with p38 MAPK activation, and positively correlated with high proliferation rates.^[7] Rex1 was found to inhibit MKK3 expression, which activates p38 MAPK. Activated p38 MAPK, in turn, inhibits proliferation. Rex1 was also found to inhibit NOTCH and STAT3, two transcription factors which lead to differentiation.^[7] Therefore, Rex1 expression allows for high levels of proliferation, and prevents differentiation through a network of various transcription factors and protein kinases.

Embryo Development

Tissue Derivation

During embryogenesis, the inner cell mass (ICM) is separated from the trophoblast. The stem cells derived from the ICM and trophectoderm have been found to express high levels of Oct3/4 and Rex1.^[8] As the ICM matures and begins to form the epiblast, and primitive ectoderm, the cells in the ICM have been found to be a heterogenous population, with varying levels of Rex1 expression. Rex1⁻/Oct3/4⁻ triggers trophectoderm differentiation, while Rex1⁺/Oct3/4⁺ cells predominantly differentiate into primitive endoderm and mesoderm.^[9] Also, Rex1⁻/Oct3/4⁺ cells differentiate into cells of primitive ectoderm, the somatic cell lineage.^[10]

Gene Control

Studies have shown that PEG3 and Nespas are downstream targets of Rex1.^[11] Rex1 can control the expression of Peg3 via epigenetic changes. YY1 has been shown to be involved in setting up DNA methylation on the maternal allele of PEG3 during oogenesis.^[12] Rex1 was found to protect the paternal allele from being methylated, and keep the PEG3 gene unmethylated during early embryogenesis.^[11] Rex1 exhibits gene control in developing embryos via its epigenetic control on genes such as PEG3, which has been identified as playing a key role in fetal growth rates ^[13]

Expression in Adult Tissues

The only adult tissue Rex1 has been identified in are the testicles. Using in situ hybridization it was determined that the spermatocytes in the more inner layers of the testicles are expressing Rex1.^[14] Thus, the male germ cells undergoing meiosis are the specific cells in the testicles that express Rex1. It has not been observed, however, that Rex1 is expressed in the female germ cells.

Rex1 Interactions with Other Transcription Factors

Rex1 participates in a network of transcription factors that all work to regulate each other via varying expression levels.

Nanog

The Nanog protein has been found to be a transcriptional activator for the Rex-1 promoter, playing a key role in sustaining Rex1 expression. Knockdown of Nanog in embryonic stem cells results in a reduction of Rex-1 expression, while forced expression of Nanog stimulates Rex-1 expression.^[1] Nanog regulates the transcription of Rex1 through 2 strong transactivation domains on the C-terminus which are required to activate the Rex1 promoter.^[1]

NOTCH

Rex1 has been found to inhibit the expression of NOTCH, thus preventing differentiation.^[7]

STAT3

Rex1 has been found to inhibit the expression of STAT3, thus preventing differentiation.^[7]

Sox2

Cooperative regulation of Rex1 is seen with Sox2 and Nanog.^[1]

Oct3/4

Oct3/4 can both repress and activate the Rex1 promoter. In cells that already express high level of Oct3/4, exogenously transfected Oct3/4 will lead to the repression of Rex1.^[15] However, in cells that are not actively expressing Oct3/4, an exogenous transfection of Oct3/4 will lead to the activation of Rex1.^[15] This implies a dual regulatory ability of Oct3/4 on Rex1. At low levels of the Oct3/4 protein, the Rex1 promoter is activated, while at high levels of the Oct3/4 protein, the Rex1 promoter is repressed.

References

Further reading

• {{cite journal |vauthors=Ota T, Suzuki Y, Nishikawa T, etal |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 }}
• {{cite journal |vauthors=Brandenberger R, Wei H, Zhang S, etal |title=Transcriptome characterization elucidates signaling networks that control human ES cell growth and differentiation. |journal=Nat. Biotechnol. |volume=22 |issue= 6 |pages= 707–16 |year= 2005 |pmid= 15146197 |doi= 10.1038/nbt971 }}
• {{cite journal |vauthors=Moriscot C, de Fraipont F, Richard MJ, etal |title=Human bone marrow mesenchymal stem cells can express insulin and key transcription factors of the endocrine pancreas developmental pathway upon genetic and/or microenvironmental manipulation in vitro. |journal=Stem Cells |volume=23 |issue= 4 |pages= 594–603 |year= 2006 |pmid= 15790780 |doi= 10.1634/stemcells.2004-0123 |url=https://archive-ouverte.unige.ch/unige:39995/ATTACHMENT01 }}
• {{cite journal |vauthors=Mongan NP, Martin KM, Gudas LJ |title=The putative human stem cell marker, Rex-1 (Zfp42): structural classification and expression in normal human epithelial and carcinoma cell cultures. |journal=Mol. Carcinog. |volume=45 |issue= 12 |pages= 887–900 |year= 2007 |pmid= 16865673 |doi= 10.1002/mc.20186 }}
• {{cite journal |vauthors=Roche S, Richard MJ, Favrot MC |title=Oct-4, Rex-1, and Gata-4 expression in human MSC increase the differentiation efficiency but not hTERT expression. |journal=J. Cell. Biochem. |volume=101 |issue= 2 |pages= 271–80 |year= 2007 |pmid= 17211834 |doi= 10.1002/jcb.21185 }}
• {{cite journal |vauthors=Rezende NC, Lee MY, Monette S, Mark W, Lu A, Gudas LJ |title=Rex1 (Zfp42) null mice show impaired testicular function, abnormal testis morphology, and aberrant gene expression.|journal=Dev. Biol. |volume=356 |issue= 2|pages= 370–82|year= 2011|pmid= 21641340 |doi=10.1016/j.ydbio.2011.05.664 |pmc=3214085}}

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