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海胆组蛋白基因的进化——紫球海胆H4基因及间隔区的核苷酸多态性

Evolving sea urchin histone genes--nucleotide polymorphisms in the H4 gene and spacers of Strongylocentrotus purpuratus.

作者信息

Yager L N, Kaumeyer J F, Weinberg E S

出版信息

J Mol Evol. 1984;20(3-4):215-26. doi: 10.1007/BF02104728.

Abstract

We present a comparison of spacer and coding sequences of histone gene repeats from four Strongylocentrotus purpuratus individuals. Sequences of two previously cloned units (pCO2 and pSp2) were compared with three new histone gene clones, two of them from a single individual. Within a 1.7-kb region, 59 polymorphic sites were found in spacers, in mRNA nontranslated stretches, and at silent sites in codons of the H4 gene. The permitted silent-site changes were as frequent as in any other region studied. The most abundant polymorphisms were single-base substitutions. The ratio of transitions : transversions : single-base-pair insertions/deletions was 3:2:2. A number of larger insertions/deletions were found, as well as differences in the length of (CTA)n and (CT)n runs. Two of the five cloned repeats contained an insertion of a 195-bp element that is also present at many other sites in the genomes of every S. purpuratus individual studied. Pairwise comparisons of the different clones indicate that the variation is not uniformly divergent, but ranges from a difference of 0.34% to 3.0% of all nucleotide sites. A parsimonious tree of ancestry constructed from the pairwise comparisons indicates that recombination between the most distantly related repeats has not occurred in the 1-2 million years necessary for accumulation of the variation. The level of sequence variation found within the S. purpuratus population, for both tandemly repeated and single-copy genes, is 25%-50% of that found between S. purpuratus and S. drobachiensis.

摘要

我们对来自四个紫海胆个体的组蛋白基因重复序列的间隔区和编码序列进行了比较。将两个先前克隆的单元(pCO2和pSp2)的序列与三个新的组蛋白基因克隆进行了比较,其中两个新克隆来自同一个体。在一个1.7kb的区域内,在间隔区、mRNA非翻译区以及H4基因密码子的沉默位点发现了59个多态性位点。允许的沉默位点变化与其他研究区域一样频繁。最丰富的多态性是单碱基替换。转换:颠换:单碱基对插入/缺失的比例为3:2:2。还发现了一些较大的插入/缺失,以及(CTA)n和(CT)n重复序列长度的差异。五个克隆重复序列中有两个包含一个195bp元件的插入,该元件在每个研究的紫海胆个体的基因组中的许多其他位点也存在。不同克隆的成对比较表明,变异并非均匀发散,而是在所有核苷酸位点的0.34%至3.0%之间变化。根据成对比较构建的简约祖先树表明,在积累变异所需的100万至200万年中,关系最遥远的重复序列之间未发生重组。在紫海胆种群中发现的串联重复基因和单拷贝基因的序列变异水平,是紫海胆和强壮海胆之间发现的变异水平的25%-50%。

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