Winter C, tom Dieck S, Boeckers T M, Bockmann J, Kämpf U, Sanmartí-Vila L, Langnaese K, Altrock W, Stumm M, Soyke A, Wieacker P, Garner C C, Gundelfinger E D
AG Molecular Neurobiology, University of Muenster, Muenster, D-48149, Germany.
Genomics. 1999 May 1;57(3):389-97. doi: 10.1006/geno.1999.5788.
Bassoon is a novel 420-kDa protein recently identified as a component of the cytoskeleton at presynaptic neurotransmitter release sites. Analysis of the rat and mouse sequences revealed a polyglutamine stretch in the C-terminal part of the protein. Since it is known for some proteins that abnormal amplification of such polyglutamine regions can cause late-onset neurodegeneration, we cloned and localized the human BASSOON gene (BSN). Phage clones spanning most of the open reading frame and the 3' untranslated region were isolated from a human genomic library and used for chromosomal localization of BSN to chromosome 3p21 by FISH. The localization was confirmed by PCR on rodent/human somatic cell hybrids; it is consistent with the localization of the murine Bsn gene at chromosome 9F. Sequencing revealed a polyglutamine stretch of only five residues in human, and PCR amplifications from 50 individuals showed no obvious length polymorphism in this region. Analysis of the primary structure of Bassoon and comparison to previous database entries provide evidence for a newly emerging protein family.
巴松管蛋白是一种新发现的420 kDa蛋白质,最近被确定为突触前神经递质释放位点细胞骨架的一个组成部分。对大鼠和小鼠序列的分析显示,该蛋白质的C末端部分存在一段多聚谷氨酰胺序列。由于已知某些蛋白质中此类多聚谷氨酰胺区域的异常扩增会导致迟发性神经退行性变,我们克隆并定位了人类巴松管蛋白基因(BSN)。从人类基因组文库中分离出跨越大部分开放阅读框和3'非翻译区的噬菌体克隆,并通过荧光原位杂交(FISH)将BSN基因定位到3号染色体的p21区域。通过对啮齿动物/人类体细胞杂种进行聚合酶链反应(PCR),证实了该定位结果;这与小鼠Bsn基因在9F染色体上的定位一致。测序结果显示,人类中的多聚谷氨酰胺序列仅由五个残基组成,对50个人进行的PCR扩增显示该区域没有明显的长度多态性。对巴松管蛋白一级结构的分析以及与先前数据库条目的比较为一个新出现的蛋白质家族提供了证据。