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RNA聚合酶II的15千道尔顿亚基对黑腹果蝇的生存能力至关重要。

The RNA polymerase II 15-kilodalton subunit is essential for viability in Drosophila melanogaster.

作者信息

Harrison D A, Mortin M A, Corces V G

机构信息

Department of Biology, Johns Hopkins University, Baltimore, Maryland 21218.

出版信息

Mol Cell Biol. 1992 Mar;12(3):928-35. doi: 10.1128/mcb.12.3.928-935.1992.

Abstract

A small, divergently transcribed gene is located 500 bp upstream of the suppressor of Hairy-wing locus of Drosophila melanogaster. Sequencing of a full-length cDNA clone of the predominant 850-nucleotide transcript reveals that this gene encodes a 15,100-Da protein with high homology to a subunit of RNA polymerase II. The RpII15 protein is 46% identical to the RPB9 protein of Saccharomyces cerevisiae, one of the smallest subunits of RNA polymerase II from that species. Among those identical residues are four pairs of cysteines whose spacing is suggestive of two metal-binding "finger" domains. The gene is expressed at all developmental stages and in all tissues. Two deletions within the RpII15 gene are multiphasic lethal deletions, with accumulation of dead animals commencing at the second larval instar. Ovary transplantation experiments indicate that survival of mutant animals to this stage is due to the persistence of maternal gene product throughout embryogenesis and early larval development. The RpII15 gene product is thus necessary for viability of D. melanogaster.

摘要

一个小的、转录方向相反的基因位于黑腹果蝇毛翅抑制基因座上游500 bp处。对占主导地位的850个核苷酸转录本的全长cDNA克隆进行测序表明,该基因编码一种15100 Da的蛋白质,与RNA聚合酶II的一个亚基具有高度同源性。RpII15蛋白与酿酒酵母的RPB9蛋白有46%的同一性,RPB9蛋白是该物种RNA聚合酶II最小的亚基之一。在这些相同的残基中有四对半胱氨酸,其间距暗示着两个金属结合“指”结构域。该基因在所有发育阶段和所有组织中均有表达。RpII15基因内的两个缺失是多相致死缺失,死亡动物的积累从第二龄幼虫期开始。卵巢移植实验表明,突变动物存活到这个阶段是由于母体基因产物在整个胚胎发育和幼虫早期发育过程中的持续存在。因此,RpII15基因产物是黑腹果蝇生存所必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cddb/369524/414c1ff7d1de/molcellb00167-0036-a.jpg

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