Suppr超能文献

由于额外性梳基因产物的母体缺陷导致果蝇同源异型基因的持续异位表达。

Persistent ectopic expression of Drosophila homeotic genes resulting from maternal deficiency of the extra sex combs gene product.

作者信息

Glicksman M A, Brower D L

机构信息

Department of Molecular and Cellular Biology, University of Arizona, Tucson 85721.

出版信息

Dev Biol. 1990 Dec;142(2):422-31. doi: 10.1016/0012-1606(90)90364-o.

Abstract

Like other members of the Polycomb group, the extra sex combs gene (esc) is required for the correct repression of loci in the major homeotic gene complexes. We show here that embryos lacking both maternal and zygotic esc+ function display transient, general derepression of both the Ultrabithorax (Ubx) and Antennapedia (Antp) genes during germ band shortening, but Sex combs reduced (Scr) expression is almost normal in the epidermis and lacking in the central nervous system (CNS). In addition, embryos that are maternally esc- but receive two paternal copies of esc+ often are characterized by ectopic expression of the three homeotic genes, especially Ubx and Antp in the CNS. Imaginal discs from these paternally rescued embryos may show discrete patches of expression of Ubx and Scr in inappropriate locations. Thus, lack of esc+ function during a brief period in early embryogenesis results in a heritable change in determined state, even in a genetically wild type animal. Within these ectopic patches, homeotic gene expression may be regulated by the disc positional fields and by cross-regulatory interactions between homeotic genes.

摘要

与多梳蛋白家族的其他成员一样,额外性梳基因(esc)对于正确抑制主要同源异型基因复合体中的基因座是必需的。我们在此表明,缺乏母源和合子esc +功能的胚胎在胚带缩短期间会短暂地普遍去抑制超双胸节基因(Ubx)和触角足基因(Antp),但性梳减少基因(Scr)在表皮中的表达几乎正常,而在中枢神经系统(CNS)中则缺乏表达。此外,母源esc - 但接受两个父源esc +拷贝的胚胎通常表现为三个同源异型基因的异位表达,特别是中枢神经系统中的Ubx和Antp。来自这些父源拯救胚胎的成虫盘可能在不适当的位置显示出Ubx和Scr的离散表达斑块。因此,即使在基因野生型动物中,早期胚胎发育短暂时期内esc +功能的缺乏也会导致决定状态的可遗传变化。在这些异位斑块内,同源异型基因的表达可能受盘位置场和同源异型基因之间的交叉调节相互作用的调控。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验