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丝状真菌棉阿舒囊霉中rRNA基因的紧密组织

Compact organization of rRNA genes in the filamentous fungus Ashbya gossypii.

作者信息

Wendland J, Pöhlmann R, Dietrich F, Steiner S, Mohr C, Philippsen P

机构信息

Lehrstuhl für Angewandte Mikrobiologie, Biozentrum, University of Basel, Klingelbergstrasse 70, CH-4056 Basel, Switzerland.

出版信息

Curr Genet. 1999 Jul;35(6):618-25. doi: 10.1007/s002940050460.

Abstract

The rDNA cluster in the phytopathogenic fungus Ashbya gossypii consists of approximately 50 tandem repeat units of 8197 bp. Each unit carries a gene for the 35S pre-rRNA, processed into 18S, 5.8S and 25S rRNA, and a divergently transcribed gene for 5S rRNA. The well-characterized rDNA of the yeast Saccharomyces cerevisiae is the only other example of a completely sequenced rDNA unit (9137 bp) carrying both a 35S pre-rRNA and a 5S rRNA gene. The coding regions for the 5S, 5.8S, 18S and 25S rRNAs are 95-100% identical whereas transcribed and non-transcribed spacers show 43-66% sequence identity. Functionally characterized rDNA and rRNA elements of S. cerevisiae can be unambiguously recognized in the A. gossypii sequence, including the RNA polymerase-I transcription start site, two Reb1p enhancer binding sites and numerous recognition sequences for rRNA modification and processing. In addition to these functionally characterized sequences eight highly conserved elements from 10 to 71 bp were detected in the over 600-bp transcribed region upstream of the 18S rRNA gene which most likely play as yet uncharacterized functions at the DNA or RNA level. In addition to this work we started to identify A. gossypii homologs of S. cerevisiae nucleolar proteins involved in rDNA maturation.

摘要

植物致病真菌棉阿舒囊霉中的核糖体DNA(rDNA)簇由大约50个8197 bp的串联重复单元组成。每个单元携带一个编码35S前体rRNA的基因,该前体rRNA可加工成18S、5.8S和25S rRNA,以及一个与5S rRNA反向转录的基因。酵母酿酒酵母中特征明确的rDNA是另一个完全测序的rDNA单元(9137 bp)的例子,它同时携带35S前体rRNA和5S rRNA基因。5S、5.8S、18S和25S rRNA的编码区有95 - 100%的同源性,而转录间隔区和非转录间隔区的序列同源性为43 - 66%。酿酒酵母中功能已明确的rDNA和rRNA元件在棉阿舒囊霉序列中能够明确识别,包括RNA聚合酶I转录起始位点、两个Reb1p增强子结合位点以及许多rRNA修饰和加工的识别序列。除了这些功能已明确的序列外,在18S rRNA基因上游超过600 bp的转录区域中检测到8个长度为10至71 bp的高度保守元件,它们很可能在DNA或RNA水平发挥尚未明确的功能。除了这项工作,我们还开始鉴定参与rDNA成熟的酿酒酵母核仁蛋白在棉阿舒囊霉中的同源物。

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