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两个间隙连接基因,连接蛋白31.1和30.3,在小鼠4号染色体上紧密连锁,并在皮肤中优先表达。

Two gap junction genes, connexin 31.1 and 30.3, are closely linked on mouse chromosome 4 and preferentially expressed in skin.

作者信息

Hennemann H, Dahl E, White J B, Schwarz H J, Lalley P A, Chang S, Nicholson B J, Willecke K

机构信息

Abteilung Molekulargenetik, Universität Bonn, Germany.

出版信息

J Biol Chem. 1992 Aug 25;267(24):17225-33.

PMID:1512260
Abstract

Two new gap junction genes isolated from the mouse genome code for connexin homologues of 271 and 266 amino acids, designated here Cx31.1 and Cx30.3, respectively. The two open reading frames, oriented in the same direction, are only 3.4 kb apart on mouse chromosome 4. Within the connexin family, these two proteins are most closely related to one another (70% amino acid sequence identity) and to Cx31 (65 and 68% identity, respectively). Comparison of the Cx31.1 mouse gene with a Cx31.1 cDNA showed a similar genomic organization to that found with other members of the connexin gene family, i.e. the coding and 3'-untranslated regions are contained within a single exon, which is preceded by an intron, less than 25 bases upstream of the ATG start codon. Northern blot hybridization revealed highly tissue-specific coexpression of the 1.6-kb Cx31.1 mRNA and two Cx30.3 transcripts of 1.9- and 3.2-kb size, predominantly in skin and two related mouse keratinocyte cell lines. Minor levels of Cx31.1 mRNA were detected in testis. Microinjection of Cx30.3, but not Cx31.1 cRNA, into Xenopus oocyte pairs induced formation of functional gap junction channels with unique voltage-gated parameters compared to other connexins expressed similarly.

摘要

从小鼠基因组中分离出的两个新的间隙连接基因编码271和266个氨基酸的连接蛋白同源物,在这里分别命名为Cx31.1和Cx30.3。这两个开放阅读框方向相同,在小鼠4号染色体上相距仅3.4 kb。在连接蛋白家族中,这两种蛋白质彼此之间关系最为密切(氨基酸序列同一性为70%),与Cx31的关系也很密切(分别为65%和68%的同一性)。将Cx31.1小鼠基因与Cx31.1 cDNA进行比较,发现其基因组结构与连接蛋白基因家族的其他成员相似,即编码区和3'非翻译区包含在一个外显子内,该外显子之前有一个内含子,位于ATG起始密码子上游不到25个碱基处。Northern印迹杂交显示,1.6 kb的Cx31.1 mRNA和1.9 kb及3.2 kb大小的两个Cx30.3转录本在组织中高度特异性共表达,主要在皮肤和两种相关的小鼠角质形成细胞系中。在睾丸中检测到少量的Cx31.1 mRNA。将Cx30.3而非Cx31.1的cRNA显微注射到非洲爪蟾卵母细胞对中,与以类似方式表达的其他连接蛋白相比,诱导形成了具有独特电压门控参数的功能性间隙连接通道。

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