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Identification and targeted disruption of the mouse gene encoding ESG1 (PH34/ECAT2/DPPA5)

BACKGROUND: Embryonic stem cell-specific gene (ESG) 1, which encodes a KH-domain containing protein, is specifically expressed in early embryos, germ cells, and embryonic stem (ES) cells. Previous studies identified genomic clones containing the mouse ESG1 gene and five pseudogenes. However, their c...

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Autores principales: Amano, Hisayuki, Itakura, Ken, Maruyama, Masayoshi, Ichisaka, Tomoko, Nakagawa, Masato, Yamanaka, Shinya
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1420271/
https://www.ncbi.nlm.nih.gov/pubmed/16504174
http://dx.doi.org/10.1186/1471-213X-6-11
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author Amano, Hisayuki
Itakura, Ken
Maruyama, Masayoshi
Ichisaka, Tomoko
Nakagawa, Masato
Yamanaka, Shinya
author_facet Amano, Hisayuki
Itakura, Ken
Maruyama, Masayoshi
Ichisaka, Tomoko
Nakagawa, Masato
Yamanaka, Shinya
author_sort Amano, Hisayuki
collection PubMed
description BACKGROUND: Embryonic stem cell-specific gene (ESG) 1, which encodes a KH-domain containing protein, is specifically expressed in early embryos, germ cells, and embryonic stem (ES) cells. Previous studies identified genomic clones containing the mouse ESG1 gene and five pseudogenes. However, their chromosomal localizations or physiological functions have not been determined. RESULTS: A Blast search of mouse genomic databases failed to locate the ESG1 gene. We identified several bacterial artificial clones containing the mouse ESG1 gene and an additional ESG1-like sequence with a similar gene structure from chromosome 9. The ESG1-like sequence contained a multiple critical mutations, indicating that it was a duplicated pseudogene. The 5' flanking region of the ESG1 gene, but not that of the pseudogene, exhibited strong enhancer and promoter activity in undifferentiated ES cells by luciferase reporter assay. To study the physiological functions of the ESG1 gene, we replaced this sequence in ES cells with a β-geo cassette by homologous recombination. Despite specific expression in early embryos and germ cells, ESG1(-/- )mice developed normally and were fertile. We also generated ESG1(-/- )ES cells both by a second independent homologous recombination and directly from blastocysts derived from heterozygous intercrosses. Northern blot and western blot analyses confirmed the absence of ESG1 in these cells. These ES cells demonstrated normal morphology, proliferation, and differentiation. CONCLUSION: The mouse ESG1 gene, together with a duplicated pseudogene, is located on chromosome 9. Despite its specific expression in pluripotent cells and germ cells, ESG1 is dispensable for self-renewal of ES cells and establishment of germcells.
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spelling pubmed-14202712006-03-30 Identification and targeted disruption of the mouse gene encoding ESG1 (PH34/ECAT2/DPPA5) Amano, Hisayuki Itakura, Ken Maruyama, Masayoshi Ichisaka, Tomoko Nakagawa, Masato Yamanaka, Shinya BMC Dev Biol Research Article BACKGROUND: Embryonic stem cell-specific gene (ESG) 1, which encodes a KH-domain containing protein, is specifically expressed in early embryos, germ cells, and embryonic stem (ES) cells. Previous studies identified genomic clones containing the mouse ESG1 gene and five pseudogenes. However, their chromosomal localizations or physiological functions have not been determined. RESULTS: A Blast search of mouse genomic databases failed to locate the ESG1 gene. We identified several bacterial artificial clones containing the mouse ESG1 gene and an additional ESG1-like sequence with a similar gene structure from chromosome 9. The ESG1-like sequence contained a multiple critical mutations, indicating that it was a duplicated pseudogene. The 5' flanking region of the ESG1 gene, but not that of the pseudogene, exhibited strong enhancer and promoter activity in undifferentiated ES cells by luciferase reporter assay. To study the physiological functions of the ESG1 gene, we replaced this sequence in ES cells with a β-geo cassette by homologous recombination. Despite specific expression in early embryos and germ cells, ESG1(-/- )mice developed normally and were fertile. We also generated ESG1(-/- )ES cells both by a second independent homologous recombination and directly from blastocysts derived from heterozygous intercrosses. Northern blot and western blot analyses confirmed the absence of ESG1 in these cells. These ES cells demonstrated normal morphology, proliferation, and differentiation. CONCLUSION: The mouse ESG1 gene, together with a duplicated pseudogene, is located on chromosome 9. Despite its specific expression in pluripotent cells and germ cells, ESG1 is dispensable for self-renewal of ES cells and establishment of germcells. BioMed Central 2006-02-28 /pmc/articles/PMC1420271/ /pubmed/16504174 http://dx.doi.org/10.1186/1471-213X-6-11 Text en Copyright © 2006 Amano et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Amano, Hisayuki
Itakura, Ken
Maruyama, Masayoshi
Ichisaka, Tomoko
Nakagawa, Masato
Yamanaka, Shinya
Identification and targeted disruption of the mouse gene encoding ESG1 (PH34/ECAT2/DPPA5)
title Identification and targeted disruption of the mouse gene encoding ESG1 (PH34/ECAT2/DPPA5)
title_full Identification and targeted disruption of the mouse gene encoding ESG1 (PH34/ECAT2/DPPA5)
title_fullStr Identification and targeted disruption of the mouse gene encoding ESG1 (PH34/ECAT2/DPPA5)
title_full_unstemmed Identification and targeted disruption of the mouse gene encoding ESG1 (PH34/ECAT2/DPPA5)
title_short Identification and targeted disruption of the mouse gene encoding ESG1 (PH34/ECAT2/DPPA5)
title_sort identification and targeted disruption of the mouse gene encoding esg1 (ph34/ecat2/dppa5)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1420271/
https://www.ncbi.nlm.nih.gov/pubmed/16504174
http://dx.doi.org/10.1186/1471-213X-6-11
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