Matsuoka Toshiki, Sato Manabu, Tokoro Mikiko, Shin Seung-Wook, Uenoyama Atsuto, Ito Kazunari, Hitomi Syuji, Amano Tomoko, Anzai Masayuki, Kato Hiromi, Mitani Tasuku, Saeki Kazuhiro, Hosoi Yoshihiko, Iritani Akira, Matsumoto Kazuya
Division of Biological Science, Graduate School of Biology-Oriented Science and Technology, Kinki University, Wakayama, Japan.
J Reprod Dev. 2008 Jun;54(3):192-7. doi: 10.1262/jrd.20008. Epub 2008 Mar 19.
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.
我们分离出一个小鼠cDNA,zag1(合子基因激活相关基因1),它有一个1728碱基对的开放阅读框,编码一个66.2 kDa的蛋白质,该蛋白质包含一个双分型核定位序列和一个含有核苷三磷酸水解酶基序的P环基序。对小鼠组织的Northern印迹分析表明,zag1广泛表达,但在卵巢和睾丸中尤为突出。对体外受精胚胎的RT-PCR分析表明,受精后卵母细胞中zag1转录本的丰度降低,并且在受精后15小时(hpi)在受精胚胎中检测到zag1 mRNA,这表明该基因在小鼠1细胞期合子基因激活开始时表达。通过对增强型绿色荧光蛋白(EGFP)标记的ZAG1进行亚细胞分析以及用抗ZAG1抗体进行免疫细胞化学分析,证实了ZAG1蛋白在15 hpi时在小鼠植入前胚胎中的核定位。随后,通过酵母双杂交筛选,我们鉴定出与前体mRNA剪接相关的U2小核核糖核蛋白B(U2B")作为ZAG1蛋白的假定相互作用伴侣。此外,用反义DNA质粒敲低zag1表达会导致注射的1细胞胚胎中胚胎发育停滞和/或延迟。这些结果表明,ZAG1可能与小鼠植入前胚胎中的合子基因表达密切相关。