Choi Seung Ho, Park Ji-Hong, Nguyen Tram Thi Ngoc, Shim Hee Jin, Song Young-Han
Ilsong Institute of Life Science, Hallym University, Anyang, Gyeonggi-do, Republic of Korea.
Department of Biomedical Gerontology, Hallym University, Chuncheon, Gangwon-do, Republic of Korea.
Dev Dyn. 2017 Jun;246(6):466-474. doi: 10.1002/dvdy.24499. Epub 2017 Apr 11.
Claspin and TopBP1 are checkpoint mediators that are required for the phosphorylation of Chk1 by ATR to maintain genomic stability. Here, we investigated the functions of Drosophila Claspin and mus101 (TopBP1 ortholog) during chorion (eggshell component) gene amplification, which occurs in follicle cells in the absence of global genomic DNA replication.
Unlike Drosophila mei-41 (ATR ortholog) mutant embryos, Claspin and mus101 mutant embryos showed severe eggshell defects resulting from defects in chorion gene amplification. EdU (5-ethynyl-2'-deoxyuridine) incorporation assay during initiation and elongation stages revealed that Claspin and mus101 were required for initiation, while only Claspin had a major role in the efficient progression of the replication forks. Claspin proteins were enriched in the amplification foci both in the initiation and elongation stage-follicle cell nuclei in a mei-41-independent manner. The focal localization of ORC2, a component of the origin recognition complex, was not significantly affected in the Claspin mutant, whereas it was reduced in the mus101 mutant.
Drosophila Claspin plays a major role in the initiation and elongation stages of chorion gene amplification by localizing to the amplification foci in a mei-41-independent manner. Drosophila mus101 is also involved in chorion gene amplification, mostly functioning in initiation, rather than elongation. Developmental Dynamics 246:466-474, 2016. © 2017 The Authors Developmental Dynamics published by Wiley Periodicals, Inc. on behalf of American Association of Anatomists.
Claspin和TopBP1是检查点介质,是ATR磷酸化Chk1以维持基因组稳定性所必需的。在此,我们研究了果蝇Claspin和mus101(TopBP1直系同源物)在绒毛膜(蛋壳成分)基因扩增过程中的功能,绒毛膜基因扩增发生在卵泡细胞中,且不存在全基因组DNA复制。
与果蝇mei-41(ATR直系同源物)突变胚胎不同,Claspin和mus101突变胚胎显示出严重的蛋壳缺陷,这是由绒毛膜基因扩增缺陷导致的。在起始和延伸阶段进行的EdU(5-乙炔基-2'-脱氧尿苷)掺入试验表明,Claspin和mus101是起始所必需的,而只有Claspin在复制叉的有效推进中起主要作用。Claspin蛋白在起始和延伸阶段的卵泡细胞核的扩增灶中均以mei-41非依赖的方式富集。起始识别复合物的一个组分ORC2的焦点定位在Claspin突变体中没有受到显著影响,而在mus101突变体中则减少。
果蝇Claspin通过以mei-41非依赖的方式定位于扩增灶,在绒毛膜基因扩增的起始和延伸阶段起主要作用。果蝇mus101也参与绒毛膜基因扩增,主要在起始阶段起作用,而不是延伸阶段。《发育动力学》2016年第246卷:466 - 474页。© 2017作者。《发育动力学》由威利期刊公司代表美国解剖学家协会出版。