| Literature DB >> 18360097 |
Toshiki Matsuoka1, Manabu Sato, Mikiko Tokoro, Seung-Wook Shin, Atsuto Uenoyama, Kazunari Ito, Syuji Hitomi, Tomoko Amano, Masayuki Anzai, Hiromi Kato, Tasuku Mitani, Kazuhiro Saeki, Yoshihiko Hosoi, Akira Iritani, Kazuya Matsumoto.
Abstract
We isolated a mouse cDNA, zag1 (zygotic gene activation-associated gene 1), that has an open reading frame of 1,728-bp encoding a protein of 66.2 kDa including both a bipartite nuclear targeting sequence and a P-loop motif containing nucleoside triphosphate hydrolase motifs. Northern blot analysis of mouse tissues showed that zag1 was widely expressed but was especially prominent in the ovary and testis. RT-PCR analysis of in vitro fertilized embryos showed that the abundance of zag1 transcripts in oocytes decreased after fertilization, and zag1 mRNA was detected at 15 h post insemination (hpi) in fertilized embryos indicating that the gene was expressed at the start of zygotic gene activation at the mouse 1-cell stage. The nuclear-localization of ZAG1 protein in mouse preimplantation embryos at 15 hpi was confirmed by both subcellular analysis of enhanced green fluorescent protein (EGFP)-tagged ZAG1 and immunocytochemical analysis with anti-ZAG1 antibody. Subsequently, using yeast two-hybrid screening, we identified U2 small nuclear ribonucleoprotein B (U2B"), which is associated with pre-mRNA splicing, as a putative interacting partner of ZAG1 protein. Furthermore, knockdown of zag1 expression by an antisense DNA plasmid induced arrest and/or delay of embryonic development in injected 1-cell embryos. These results suggest that ZAG1 may be closely associated with zygotic gene expression in mouse preimplantation embryos.Entities:
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Year: 2008 PMID: 18360097 DOI: 10.1262/jrd.20008
Source DB: PubMed Journal: J Reprod Dev ISSN: 0916-8818 Impact factor: 2.214