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一种秀丽隐杆线虫RNA聚合酶II基因,ama-1 IV,以及附近的必需基因。

A Caenorhabditis elegans RNA polymerase II gene, ama-1 IV, and nearby essential genes.

作者信息

Rogalski T M, Riddle D L

机构信息

Division of Biological Sciences, University of Missouri, Columbia, 65211, USA.

出版信息

Genetics. 1988 Jan;118(1):61-74. doi: 10.1093/genetics/118.1.61.

Abstract

The amanitin-binding subunit of RNA polymerase II in Caenorhabditis elegans is encoded by the ama-1 gene, located approximately 0.05 map unit to the right of dpy-13 IV. Using the amanitin-resistant ama-1(m118) strain as a parent, we have isolated amanitin-sensitive mutants that carry recessive-lethal ama-1 alleles. Of the six ethyl methanesulfonate-induced mutants examined, two are arrested late in embryogenesis. One of these is a large deficiency, mDf9, but the second may be a novel point mutation. The four other mutants are hypomorphs, and presumably produce altered RNA polymerase II enzymes with some residual function. Two of these mutants develop into sterile adults at 20 degrees but are arrested as larvae at 25 degrees, and two others are fertile at 20 degrees and sterile at 25 degrees. Temperature-shift experiments performed with the adult sterile mutant, ama-1(m118m238ts), have revealed a temperature-sensitive period that begins late in gonadogenesis and is centered around the initiation of egg-laying. Postembryonic development at 25 degrees is slowed by 30%. By contrast, the amanitin-resistant allele of ama-1 has very little effect on developmental rate or fertility. We have identified 15 essential genes in an interval of 4.5 map units surrounding ama-1, as well as four gamma-ray-induced deficiencies and two duplications that include the ama-1 gene. The larger duplication, mDp1, may include the entire left arm of chromosome IV, and it recombines with the normal homologue at a low frequency. The smallest deficiency, mDf10, complements all but three identified genes: let-278, dpy-13 and ama-1, which define an interval of only 0.1 map unit. The terminal phenotype of mDf10 homozygotes is developmental arrest during the first larval stage, suggesting that there is sufficient maternal RNA polymerase II to complete embryonic development.

摘要

秀丽隐杆线虫RNA聚合酶II的鹅膏毒肽结合亚基由ama-1基因编码,该基因位于dpy-13四号染色体右侧约0.05个图距单位处。以抗鹅膏毒肽的ama-1(m118)品系作为亲本,我们分离出了携带隐性致死ama-1等位基因的鹅膏毒肽敏感突变体。在所检测的6个经甲磺酸乙酯诱导的突变体中,有2个在胚胎发育后期停滞。其中一个是大片段缺失,即mDf9,但另一个可能是新的点突变。其他4个突变体是亚效等位基因,推测产生了具有一些残余功能的改变的RNA聚合酶II酶。其中2个突变体在20摄氏度时发育成不育成虫,但在25摄氏度时停滞为幼虫,另外2个在20摄氏度时可育,在25摄氏度时不育。对成年不育突变体ama-1(m118m238ts)进行的温度转换实验揭示了一个温度敏感期,该时期始于性腺发育后期,以产卵开始为中心。25摄氏度时的胚后发育减缓了30%。相比之下,ama-1的抗鹅膏毒肽等位基因对发育速率或育性影响很小。我们在围绕ama-1的4.5个图距单位区间内鉴定出了15个必需基因,以及4个γ射线诱导的缺失和2个包含ama-1基因的重复。较大的重复mDp1可能包含四号染色体的整个左臂,并且它与正常同源物以低频率重组。最小的缺失mDf10除了let-278、dpy-13和ama-1这3个已鉴定基因外,对其他所有基因都有互补作用,这3个基因定义了一个仅0.1个图距单位的区间。mDf10纯合子的终末表型是在第一幼虫阶段发育停滞,这表明有足够的母体RNA聚合酶II来完成胚胎发育。

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