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一个复杂基因座的结构与调控:果蝇的cut基因

Structure and regulation of a complex locus: the cut gene of Drosophila.

作者信息

Jack J, DeLotto Y

机构信息

Department of Anatomy, University of Connecticut Health Center, Framington 06030, USA.

出版信息

Genetics. 1995 Apr;139(4):1689-700. doi: 10.1093/genetics/139.4.1689.

Abstract

The cut locus encodes a homeobox protein that is localized in the nuclei of a variety of tissues and is required for proper morphogenesis of those tissues. Cut protein is required in embryonic and adult external sensory organs, where its absence results in conversion of the organs to chordotonal organs. Expression of cut also occurs in the Malpighian tubules, spiracles, central nervous system, and a number of other tissues. Gypsy transposon insertions upstream of the cut promoter block expression in subsets of these tissues. The effect of the gypsy insertions is polar, with those farthest from the promoter affecting the fewest tissues. The hypothesis that gypsy insertions block a series of tissue-specific enhancer elements that are distributed over a region of 80 kb upstream of the promoter predicts the location of the enhancers for cut expression in each of the tissues in which it is active in embryos. DNA fragments from this region drive expression of a reporter gene in each of the embryonic tissues in which endogenous cut gene is expressed. Each tissue has its own enhancer, and none of the enhancers require the activity of the endogenous cut gene to function.

摘要

切割位点编码一种同源异型框蛋白,该蛋白定位于多种组织的细胞核中,是这些组织正常形态发生所必需的。在胚胎和成年期的外部感觉器官中需要切割蛋白,其缺失会导致这些器官转变为弦音器官。切割蛋白的表达也发生在马氏管、气门、中枢神经系统和许多其他组织中。位于切割启动子上游的吉普赛转座子插入会阻断这些组织亚群中的表达。吉普赛插入的影响是极性的,离启动子最远的那些插入影响的组织最少。吉普赛插入阻断一系列组织特异性增强子元件的假说,这些元件分布在启动子上游80 kb的区域,该假说预测了切割蛋白在胚胎中活跃的每个组织中的表达增强子的位置。来自该区域的DNA片段驱动报告基因在每个内源性切割基因表达的胚胎组织中表达。每个组织都有自己的增强子,并且没有一个增强子需要内源性切割基因的活性来发挥作用。

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本文引用的文献

1
Analysis of the Cut Locus of DROSOPHILA MELANOGASTER.黑腹果蝇的切割轨迹分析。
Genetics. 1979 Jun;92(2):485-502. doi: 10.1093/genetics/92.2.485.
8
From DNA to form: the achaete-scute complex.从DNA到形态:achaete - scute复合体
Genes Dev. 1988 May;2(5):495-501. doi: 10.1101/gad.2.5.495.

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