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DNA超螺旋因子正向调控果蝇同源异型基因Abdominal-B的表达。

DNA supercoiling factor positively regulates expression of the homeotic gene Abdominal-B in Drosophila melanogaster.

作者信息

Ogasawara Youhei, Furuhashi Hirofumi, Hirose Susumu

机构信息

Department of Developmental Genetics, National Institute of Genetics, and Department of Genetics, SOKENDAI, Mishima, Shizuoka-ken 411-8540, Japan.

出版信息

Genes Cells. 2007 Dec;12(12):1347-55. doi: 10.1111/j.1365-2443.2007.01140.x.

DOI:10.1111/j.1365-2443.2007.01140.x
PMID:18076572
Abstract

DNA supercoiling factor (SCF) generates unconstrained negative supercoils of DNA in conjunction with eukaryotic topoisomerase II. In Drosophila melanogaster, SCF localizes to puffs on polytene chromosomes and is required for dosage compensation via hypertranscripton of genes on the male X chromosome. The present study investigated the role of SCF on autosomes. Although RNAi knockdown of scf results in male lethality, some escapers showed anterior homeotic transformation of the male sixth abdominal segment, similar to that arising from reduced expression of Abdominal-B (Abd-B). Heterozygotes for an scf mutant allele (scf(1)) displayed suppression of Pc mutation-dependent posterior transformation and enhancement of anterior transformation caused by trxG mutations. The level of Abd-B mRNA decreased in scf(1) embryos compared with wild-type. Tiling array experiments showed the presence of significant SCF signals in an Abd-B promoter region. Expression from the basal Abd-B promoter on a transgene was reduced in scf(1) embryos compared with wild-type. Collectively, these results demonstrate that SCF occupies the promoter region of Abd-B and activates expression for the proper formation of abdominal segments. Furthermore, preferential occupancy of SCF around transcription start sites of many active genes suggests a role for the factor in positive regulation of promoters.

摘要

DNA超螺旋因子(SCF)与真核拓扑异构酶II共同作用产生无约束的DNA负超螺旋。在黑腹果蝇中,SCF定位于多线染色体的胀泡上,并且是通过雄性X染色体上基因的超转录实现剂量补偿所必需的。本研究调查了SCF在常染色体上的作用。虽然scf的RNA干扰敲低导致雄性致死,但一些存活者表现出雄性第六腹节的前部同源异型转化,类似于因腹部B(Abd-B)表达降低而产生的转化。scf突变等位基因(scf(1))的杂合子表现出对Pc突变依赖性后部转化的抑制以及trxG突变引起的前部转化的增强。与野生型相比,scf(1)胚胎中Abd-B mRNA的水平降低。平铺阵列实验表明在Abd-B启动子区域存在显著的SCF信号。与野生型相比,scf(1)胚胎中转基因上基础Abd-B启动子的表达降低。总体而言,这些结果表明SCF占据Abd-B的启动子区域并激活表达以促进腹节的正常形成。此外,SCF在许多活跃基因转录起始位点周围的优先占据表明该因子在启动子的正调控中发挥作用。

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