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编码小鼠S16核糖体蛋白的多基因家族的特征分析:通过对总基因组DNA的分析来区分一个表达基因与其加工假基因对应物的策略。

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.

作者信息

Wagner M, Perry R P

出版信息

Mol Cell Biol. 1985 Dec;5(12):3560-76. doi: 10.1128/mcb.5.12.3560-3576.1985.

Abstract

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.

摘要

克隆、测序并分析了小鼠核糖体蛋白S16家族的两个基因。其中一个基因是加工假基因,即可能来源于mRNA中间体的无功能基因。另一个S16基因含有内含子,其外显子序列与克隆的S16 cDNA相同。通过用cDNA和独特序列内含子探针进行核多聚腺苷酸(poly(A)+)RNA的Northern印迹分析,证实了该基因的表达。每个S16内含子都包含TACTAAC基序的一个保存完好的残余部分,该基序在酵母内含子中普遍存在,并且已知在剪接中起关键作用。与我们实验室分析的另外两个小鼠核糖体蛋白基因L30和L32进行序列比较,发现了可能参与核糖体蛋白基因表达控制和协调的共同结构特征。这些特征包括在-20至-30区域缺乏典型的TATA框,以及跨越帽位点且两侧为富含C+G序列的显著相似的12个核苷酸嘧啶序列(CTTCCYTYYTC)。通过三种实验评估了S16家族其他成员的性质:用于测量染色质凝聚程度的DNA酶I敏感性分析;用于估计每个基因序列与表达基因序列差异程度的cDNA-基因杂交体热稳定性分析;以及区分含内含子基因和无内含子加工基因的限制性片段分析。这些分析结果表明,除了表达的S16基因外,所有基因都处于与转录静止相关的凝聚染色质构型;S16家族中的大多数基因与表达的S16基因序列差异大于7%;并且10个S16基因中至少有7个缺乏内含子。我们得出结论,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型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05ab/369187/cf36cfb04724/molcellb00142-0242-a.jpg

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