首页> 外文OA文献 >Characterization of the multigene family encoding the mouse S16 ribosomal protein: strategy for distinguishing an expressed gene from its processed pseudogene counterparts by an analysis of total genomic DNA.
【2h】

Characterization of the multigene family encoding the mouse S16 ribosomal protein: strategy for distinguishing an expressed gene from its processed pseudogene counterparts by an analysis of total genomic DNA.

机译:编码小鼠S16核糖体蛋白的多基因家族的表征:通过分析总基因组DNA区分表达的基因与其加工的假基因对应物的策略。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Two genes from the family encoding mouse ribosomal protein S16 were cloned, sequenced, and analyzed. One gene was found to be a processed pseudogene, i.e., a nonfunctional gene presumably derived from an mRNA intermediate. The other S16 gene contained introns and had exonic sequences identical to those of a cloned S16 cDNA. The expression of this gene was demonstrated by Northern blot analysis of nuclear poly(A)+ RNA with cDNA and unique sequence intron probes. Each S16 intron contains a well-preserved remnant of the TACTAAC motif, which is ubiquitous in yeast introns and known to play a critical role in intron splicing. A sequence comparison with two other mouse ribosomal protein genes analyzed in our laboratory, L30 and L32, revealed common structural features which might be involved in the control and coordination of ribosomal protein gene expression. These include the lack of a canonical TATA box in the -20 to -30 region and a remarkably similar 12-nucleotide pyrimidine sequence (CTTCCYTYYTC) that spans the cap site and is flanked by C + G-rich sequences. The nature of the other members of the S16 family was evaluated by three types of experiment: a DNase I sensitivity analysis to measure the extent of chromatin condensation; an analysis of the thermal stability of cDNA-gene hybrids to estimate the extent of divergence of each gene sequence from that of the expressed gene; and a restriction fragment analysis which distinguishes intron-containing genes from intronless processed genes. The results of these analyses show that all genes except the expressed S16 gene are in a condensed chromatin configuration associated with transcriptional quiescence; that most of the genes within the S16 family have sequences greater than 7% divergent from the expressed S16 gene; and that at least 7 of the 10 S16 genes lack introns. We conclude that the ribosomal protein S16 multigene family contains one expressed intron-containing gene and nine inactive pseudogenes, most or all of which are of the processed type.
机译:来自编码小鼠核糖体蛋白S16的家族的两个基因被克隆,测序和分析。发现一个基因是经加工的假基因,即,推测是衍生自mRNA中间体的非功能性基因。另一个S16基因含有内含子,外显子序列与克隆的S16 cDNA相同。该基因的表达通过核聚(A)+ RNA,cDNA和独特序列内含子探针的Northern印迹分析证实。每个S16内含子都包含一个保存完好的TACTAAC基序,该基序在酵母内含子中无处不在,并且在内含子剪接中起着至关重要的作用。与在我们的实验室L30和L32中分析的其他两个小鼠核糖体蛋白基因的序列比较揭示了可能与核糖体蛋白基因表达的控制和协调有关的共同结构特征。这些包括在-20至-30区域中缺少规范的TATA框,以及跨帽区且侧接富含C + G序列的非常相似的12个核苷酸的嘧啶序列(CTTCCYTYYTC)。通过三种类型的实验评估了S16家族其他成员的性质:DNase I敏感性分析,用于测量染色质凝聚的程度;分析cDNA-基因杂种的热稳定性,以估算每个基因序列与表达基因的差异程度;限制性片段分析,将含内含子的基因与无内含子的加工基因区分开。这些分析的结果表明,除表达的S16基因外,所有基因均处于与转录静止相关的浓缩染色质构型。 S16家族中的大多数基因与所表达的S16基因的序列差异大于7%; 10个S16基因中至少有7个缺乏内含子。我们得出的结论是,核糖体蛋白S16多基因家族包含一个表达的含内含子基因和九个无活性假基因,其中大多数或全部为加工类型。

著录项

  • 作者

    Wagner, M; Perry, R P;

  • 作者单位
  • 年度 1985
  • 总页数
  • 原文格式 PDF
  • 正文语种 en
  • 中图分类

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号