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小鼠马珠蛋白-3基因(Matn3)的结构与定位,该基因是一个包含U12型AT-AC内含子的基因家族的成员。

Structure and mapping of the mouse matrilin-3 gene (Matn3), a member of a gene family containing a U12-type AT-AC intron.

作者信息

Wagener R, Kobbe B, Aszódi A, Liu Z, Beier D R, Paulsson M

机构信息

Institute for Biochemistry, Medical Faculty, University of Cologne, Germany.

出版信息

Mamm Genome. 2000 Feb;11(2):85-90. doi: 10.1007/s003350010018.

Abstract

The gene for murine matrilin-3, an extracellular matrix protein present in cartilage, was isolated and further characterized. The gene spans 23.4 kb and comprises 8 exons; with one exception, this reflects the modular structure of the protein. The major and a minor transcription start site were determined by RNase protection assays to positions approximately 72 nt and 87 nt upstream of the ATG codon, respectively. The promoter contains a TATA-like box 32 bp upstream of the main transcription start as well as several potential binding sites for eukaryotic transcription factors. As in all known matrilin genes, the last intron, separating the exons coding for the coiled-coil domain, does not follow the GT-AG rule and belongs to the subgroup of introns having AT-AC at the ends that are spliced by the U12-type spliceosome. The mouse matrilin-3 gene does not contain hidden exon sequences coding for the second vWFA-like domain present in all other matrilins. The intron that could possibly contain such sequences instead shows 75% repetitive sequences, indicating an evolutionary process that has led to the loss of sequences coding for vWFA2. Single-strand conformation polymorphism analysis was used to map the Matn3 gene to the proximal end of Chr 12, linked to the genes Synd1, Apob, Dntb, and Kif3c.

摘要

分离并进一步鉴定了小鼠基质金属蛋白酶-3(一种存在于软骨中的细胞外基质蛋白)的基因。该基因跨度为23.4 kb,包含8个外显子;除了一个例外,这反映了该蛋白质的模块化结构。通过核糖核酸酶保护试验确定主要和次要转录起始位点分别位于ATG密码子上游约72 nt和87 nt处。启动子在主要转录起始位点上游32 bp处含有一个类TATA盒以及几个真核转录因子的潜在结合位点。与所有已知的基质金属蛋白酶基因一样,分隔编码卷曲螺旋结构域的外显子的最后一个内含子不遵循GT-AG规则,属于在末端具有AT-AC且由U12型剪接体剪接的内含子亚组。小鼠基质金属蛋白酶-3基因不包含编码所有其他基质金属蛋白酶中存在的第二个vWFA样结构域的隐藏外显子序列。可能包含此类序列的内含子反而显示出75%的重复序列,表明这是一个导致vWFA2编码序列丢失的进化过程。利用单链构象多态性分析将Matn3基因定位到12号染色体近端,与Synd1、Apob、Dntb和Kif3c基因连锁。

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