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髓磷脂蛋白脂蛋白基因结构及其在正常和震颤突变小鼠中的表达调控。

Myelin proteolipid protein gene structure and its regulation of expression in normal and jimpy mutant mice.

作者信息

Ikenaka K, Furuichi T, Iwasaki Y, Moriguchi A, Okano H, Mikoshiba K

机构信息

Institute for Protein Research, Osaka University, Japan.

出版信息

J Mol Biol. 1988 Feb 20;199(4):587-96. doi: 10.1016/0022-2836(88)90303-8.

Abstract

The mouse proteolipid protein (PLP) gene was cloned into the lambda bacteriophage Charon 4A. The organization and the nucleotide sequence of the exons of the mouse PLP gene were quite similar to those of their human counterparts, consisting of seven exons. The transcription of the PLP gene started from multiple sites. There was a unique sequence tandemly repeated four times, sharing homology with the herpes simplex virus DR2 sequence, upstream from the transcribed region. Expression of the myelin basic protein (MBP) is also restricted to the oligodendrocytes in the central nervous system as is the PLP expression. Homology search against the mouse MBP gene revealed that several boxes in the 5'-flanking region of PLP show a high degree of homology with the sequence present in the MBP 5'-flanking region, possibly of importance in the concomitant expression of both genes in the central nervous system. PLP-mRNA in jimpy mutant mice does not contain exon 5 and its content is greatly reduced. We analyzed the jimpy PLP-mRNA and showed that the transcription initiated from the same sites as those in normal mice. Cloning and sequencing of the 5'-flanking region of the jimpy PLP gene revealed that there were no mutations in the promoter region of the jimpy PLP gene. Therefore, it is likely that a mutation, presumably existing within the jimpy PLP gene, caused the skipping of exon 5 and directly affected the mRNA level.

摘要

小鼠蛋白脂蛋白(PLP)基因被克隆到λ噬菌体Charon 4A中。小鼠PLP基因外显子的组织和核苷酸序列与其人类对应物非常相似,由七个外显子组成。PLP基因的转录起始于多个位点。在转录区域上游有一个独特的序列串联重复四次,与单纯疱疹病毒DR2序列具有同源性。髓鞘碱性蛋白(MBP)的表达也像PLP表达一样局限于中枢神经系统的少突胶质细胞。对小鼠MBP基因的同源性搜索显示,PLP 5'侧翼区域的几个框与MBP 5'侧翼区域中存在的序列具有高度同源性,这可能对这两个基因在中枢神经系统中的伴随表达很重要。jimpy突变小鼠中的PLP - mRNA不包含外显子5,其含量大大降低。我们分析了jimpy PLP - mRNA,并表明转录起始于与正常小鼠相同的位点。jimpy PLP基因5'侧翼区域的克隆和测序显示,jimpy PLP基因的启动子区域没有突变。因此,很可能是jimpy PLP基因内可能存在的一个突变导致了外显子5的缺失,并直接影响了mRNA水平。

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