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可被毛翅抑制子抑制的黑腹果蝇突变是一个7.3千碱基移动元件的插入。

Drosophila melanogaster mutations suppressible by the suppressor of Hairy-wing are insertions of a 7.3-kilobase mobile element.

作者信息

Modolell J, Bender W, Meselson M

出版信息

Proc Natl Acad Sci U S A. 1983 Mar;80(6):1678-82. doi: 10.1073/pnas.80.6.1678.

Abstract

Certain spontaneous mutations of Drosophila melanogaster are suppressed by su(Hw), the suppressor of Hairy-wing (3R-54.8). We find that mutations suppressible by su(Hw) result from insertions of a mobile element at the affected loci. The element, named gypsy, is approximately 7.3 kilobases long and includes 0.5-kilobase direct terminal repeats. It was first identified in DNA cloned from the bithorax chromosomal region of several Drosophila stocks carrying suppressible mutations of the bithorax complex. Cloned gypsy DNA was used as a probe to test for the association of gypsy with suppressible mutations at various other loci by hybridization in situ. Gypsy was found to be associated with 19 suppressible alleles at 10 different loci: yellow, Hairy-wing, scute, diminutive, cut, lozenge, forked, Beadex, hairy, and the bithorax complex. It was found with wild-type or nonsuppressible mutations at any of these loci. Gypsy DNA was also used as a probe to clone the element and adjacent unique DNA from the loci of some suppressible mutations. This confirmed the presence of the full-length element and also provided cloned DNA from the previously uncloned loci scute and cut. The suppressor of Hairy-wing is generally recessive and behaves as a null mutation. Thus, the disruption of normal gene function caused by the inserted gypsy element appears to require some product of the wild-type suppressor gene, su(Hw)+.

摘要

黑腹果蝇的某些自发突变会被毛翅抑制因子(3R-54.8)su(Hw)所抑制。我们发现可被su(Hw)抑制的突变是由一个可移动元件插入到受影响位点所致。该元件名为gypsy,长度约为7.3千碱基,包含0.5千碱基的直接末端重复序列。它最初是在从几种携带双胸复合体可抑制突变的果蝇品系的双胸染色体区域克隆的DNA中被鉴定出来的。克隆的gypsy DNA被用作探针,通过原位杂交来检测gypsy与其他各个位点的可抑制突变之间的关联。结果发现gypsy与10个不同位点的19个可抑制等位基因相关:黄色、毛翅、盾片、矮小、切割、菱形、叉状、珠饰、多毛以及双胸复合体。在这些位点的任何一个野生型或不可抑制突变中均未发现gypsy。gypsy DNA还被用作探针,从一些可抑制突变的位点克隆该元件及相邻的独特DNA。这证实了全长元件的存在,同时也提供了来自之前未克隆位点盾片和切割的克隆DNA。毛翅抑制因子通常是隐性的,表现为无效突变。因此,插入的gypsy元件导致的正常基因功能破坏似乎需要野生型抑制基因su(Hw)+的某些产物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6d4/393666/f6a11aa00dbe/pnas00632-0200-a.jpg

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