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大鼠金属硫蛋白-1结构基因和三个假基因,其中一个含有5'调控序列。

Rat metallothionein-1 structural gene and three pseudogenes, one of which contains 5'-regulatory sequences.

作者信息

Andersen R D, Birren B W, Taplitz S J, Herschman H R

出版信息

Mol Cell Biol. 1986 Jan;6(1):302-14. doi: 10.1128/mcb.6.1.302-314.1986.

Abstract

As shown by Southern blot analysis, the metallothionein-1 (MT-1) genes in rats comprise a multigene family. We present the sequence of the MT-1 structural gene and compare its features with other metallothionein genes. Three MT-1 pseudogenes which we sequenced apparently arose by reverse transcription of processed mRNA transcripts. Two of these, MT-1 psi a and MT-1 psi c, are retrogenes which derive from the MT-1 mRNA, having diverged from the MT-1 gene 6.9 and 2.6 million years ago, respectively. The third, MT-1 psi b, differs from the MT-1 cDNA by only three nucleotide alterations. Surprisingly, MT-1 psi b also preserves sequence homology for 142 base pairs 5' to the transcription initiation site of the parent gene; it contains a promoter sequence sufficient for specifying metal ion induction. We identified, by S1 nuclease mapping, an RNA polymerase II initiation site 432 base pairs 5' of the MT-1 transcription initiation site of the MT-1 structural gene which could explain the formation of the mRNA precursor to this pseudogene. We were unable to detect MT-1 psi b transcripts, either in liver tissue or after transfection. We conclude that the absence of detectable transcripts from this pseudogene is due to either a reduced level of transcription or the formation of unstable transcripts as a consequence of the lack of a consensus sequence normally found 3' of transcription termination in the MT-1 structural gene.

摘要

Southern印迹分析表明,大鼠中的金属硫蛋白-1(MT-1)基因构成一个多基因家族。我们给出了MT-1结构基因的序列,并将其特征与其他金属硫蛋白基因进行了比较。我们测序的三个MT-1假基因显然是由加工后的mRNA转录本逆转录产生的。其中两个,MT-1 psi a和MT-1 psi c,是分别在690万年前和260万年前从MT-1 mRNA分化而来的反转录基因。第三个,MT-1 psi b,与MT-1 cDNA仅在三个核苷酸上存在差异。令人惊讶的是,MT-1 psi b在亲本基因转录起始位点上游142个碱基对处也保留了序列同源性;它包含一个足以指定金属离子诱导的启动子序列。我们通过S1核酸酶图谱分析,在MT-1结构基因的MT-1转录起始位点上游432个碱基对处鉴定出一个RNA聚合酶II起始位点,这可以解释该假基因mRNA前体的形成。我们在肝组织中或转染后均未能检测到MT-1 psi b转录本。我们得出结论,该假基因无法检测到转录本是由于转录水平降低或由于MT-1结构基因转录终止位点下游通常缺乏共有序列而形成不稳定转录本所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c990/367511/fe2089c580d4/molcellb00085-0322-a.jpg

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