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网织蛋白基因家族新成员(RTN3)的克隆:基因结构及染色体定位于11q13

Cloning of a novel member of the reticulon gene family (RTN3): gene structure and chromosomal localization to 11q13.

作者信息

Moreira E F, Jaworski C J, Rodriguez I R

机构信息

Laboratory of Retinal Cell and Molecular Biology, National Eye Institute, Bethesda, Maryland 20892, USA.

出版信息

Genomics. 1999 May 15;58(1):73-81. doi: 10.1006/geno.1999.5807.

Abstract

A novel member of the neuron-specific protein (NSP) or newly named reticulon (RTN) gene family was isolated during a subtraction cloning between macula and peripheral retina. The mRNA for this NSP/RTN-like gene is approximately threefold more abundant in macula than in peripheral retina. The cDNA is 2527 bp long and contains an open reading frame of 236 amino acids. The deduced peptide shows a strong similarity to the NSP/RTN and tropomyosin-like gene families but it is clearly a novel member. The gene contains seven exons and spans more than 15 kb. The gene was localized to chromosome 11q13 between markers D11S4535 and D11S4627 using somatic cell hybrid panels. Southern blot analysis identified the presence of a pseudogene(s) that was subsequently localized to chromosome 4. Multitissue Northern blot analysis found this gene to be widely expressed in human tissues with the highest expression in the brain. We are calling this gene RTN3 to reflect the newly proposed nomenclature.

摘要

在黄斑与周边视网膜的消减克隆过程中,分离出了神经元特异性蛋白(NSP)或新命名的网织蛋白(RTN)基因家族的一个新成员。该NSP/RTN样基因的mRNA在黄斑中的丰度比在周边视网膜中大约高三倍。cDNA长2527 bp,包含一个236个氨基酸的开放阅读框。推导的肽段与NSP/RTN和原肌球蛋白样基因家族有很强的相似性,但它显然是一个新成员。该基因包含七个外显子,跨度超过15 kb。利用体细胞杂交板将该基因定位到11号染色体q13区的D11S4535和D11S4627标记之间。Southern印迹分析确定存在一个假基因,随后将其定位到4号染色体。多组织Northern印迹分析发现该基因在人类组织中广泛表达,在脑中表达最高。我们将这个基因命名为RTN3以反映新提出的命名法。

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