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酿酒酵母克隆的和基因组rDNA非转录间隔区内长度异质性的规则分布。

Regular distribution of length heterogeneities within non-transcribed spacer regions of cloned and genomic rDNA of Saccharomyces cerevisiae.

作者信息

Jemtland R, Maehlum E, Gabrielsen O S, Oyen T B

出版信息

Nucleic Acids Res. 1986 Jul 11;14(13):5145-58. doi: 10.1093/nar/14.13.5145.

Abstract

A length difference of about 50 bp in the EcoRI fragment B of the rDNA from two different strains of Saccharomyces cerevisiae has been mapped in detail by sequencing of cloned fragments. This 2.4 kb EcoRI fragment contains the start of the 35S rRNA gene at one end and the 5S rRNA gene in the middle flanked by non-transcribed spacers, NTS1 and NTS2. The difference appeared as short deletions or insertions in five regularly spaced regions within the 1 kb NTS1, 3' to the 5S rRNA gene. The same regions of heterogeneities were displayed when all available sequence data of the NTS1 were compared. Four of the variable regions are located 160-170 bp apart, indicating that they might represent linker sequences between phased nucleosomes. Two variant clones, differing in the length of one subfragment of NTS1, were isolated for each strain. In both cases these represented the major variants among chromosomal NTS1 as revealed by sequencing of genomic fragments.

摘要

通过对克隆片段进行测序,已详细绘制出酿酒酵母两个不同菌株的rDNA的EcoRI片段B中约50 bp的长度差异。这个2.4 kb的EcoRI片段一端包含35S rRNA基因的起始位点,中间是5S rRNA基因,两侧为非转录间隔区NTS1和NTS2。差异表现为1 kb的NTS1(位于5S rRNA基因3'端)内五个规则间隔区域中的短缺失或插入。当比较NTS1的所有可用序列数据时,显示出相同的异质性区域。四个可变区域相隔160 - 170 bp,表明它们可能代表相控核小体之间的连接序列。针对每个菌株分离出两个NTS1一个亚片段长度不同的变体克隆。在这两种情况下,如通过基因组片段测序所揭示的,这些代表了染色体NTS1中的主要变体。

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