Molecular Cloning and Functional Analysis of ESGP, an Embryonic Stem Cell and Germ Cell Specific Protein

Several putative Oct‐4 downstream genes from mouse embryonic stem (ES) cells have been identified using the suppression‐subtractive hybridization method. In this study, one of the novel genes encoding an ES cell and germ cell specific protein (ESGP) was cloned by rapid amplification of cDNA ends. ES...

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Published inActa biochimica et biophysica Sinica Vol. 37; no. 12; pp. 789 - 796
Main Authors CHEN, Yan‐Mei, DU, Zhong‐Wei, YAO, Zhen
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Science Pty 01.12.2005
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Summary:Several putative Oct‐4 downstream genes from mouse embryonic stem (ES) cells have been identified using the suppression‐subtractive hybridization method. In this study, one of the novel genes encoding an ES cell and germ cell specific protein (ESGP) was cloned by rapid amplification of cDNA ends. ESGP contains 801 bp encoding an 84 amino acid small protein and has no significant homology to any known genes. There is a signal peptide at the N‐terminal of ESGP protein as predicted by SeqWeb (GCG) (SeqWeb version 2.0.2, http://gcg.biosino.org:8080/). The result of immunofluorescence assay suggested that ESGP might encode a secretory protein. The expression pattern of ESGP is consistent with the expression of Oct‐4 during embryonic development. ESGP protein was detected in fertilized oocyte, from 3.5 day postcoital (dpc) blastocyst to 17.5 dpc embryo, and was only detected in testis and ovary tissues in adult. In vitro, ESGP was only expressed in pluripotent cell lines, such as embryonic stem cells, embryonic carcinoma cells and embryonic germ cells, but not in their differentiated progenies. Despite its specific expression, forced expression of ESGP is not indispensable for the effect of Oct‐4 on ES cell self‐renewal, and does not affect the differentiation to three germ layers. Edited by Xiao‐Yan DING
Bibliography:zhongweidu@wisc.edu
Department of Anatomy, School of Medicine, Waisman Center, Wicell Institute, University of Wisconsin, Madison, WI 53705, USA. E‐mail
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ISSN:1672-9145
1745-7270
DOI:10.1111/j.1745-7270.2005.00120.x