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将GM2激活蛋白(GM2A)基因座精细定位到5q31.3 - q33.1,位于脊髓性肌萎缩基因座的远端。

Refined mapping of the GM2 activator protein (GM2A) locus to 5q31.3-q33.1, distal to the spinal muscular atrophy locus.

作者信息

Heng H H, Xie B, Shi X M, Tsui L C, Mahuran D J

机构信息

Department of Molecular and Medical Genetics, University of Toronto, Ontario, Canada.

出版信息

Genomics. 1993 Nov;18(2):429-31. doi: 10.1006/geno.1993.1491.

Abstract

The GM2 activator locus (GM2A) had previously been considered as a candidate gene for some forms of spinal muscular atrophy (SMA; mapped to 5q11.2-q13.3). It was eliminated as a possible candidate because PCR-based mapping failed to localize the gene to chromosome 5, as was previously reported using an ELISA-based methodology. However, we demonstrated that the PCR primers used preferentially amplified a processed pseudogene (GM2AP) that we mapped to chromosome 3 and that GM2A was located on chromosome 5. In this report, we reconsider the candidacy of GM2A by refining its localization on chromosome 5 using fluorescence in situ hybridization. We localize GM2A to 5q31.3-q33.1; thus, it is not a candidate gene for SMA.

摘要

GM2激活剂基因座(GM2A)此前被认为是某些形式脊髓性肌萎缩症(SMA;定位于5q11.2-q13.3)的候选基因。它被排除在可能的候选基因之外,因为基于聚合酶链反应(PCR)的定位未能将该基因定位于5号染色体,此前使用基于酶联免疫吸附测定(ELISA)的方法曾有过相关报道。然而,我们证明所使用的PCR引物优先扩增了一个加工假基因(GM2AP),我们将其定位于3号染色体,而GM2A位于5号染色体上。在本报告中,我们通过使用荧光原位杂交技术优化GM2A在5号染色体上的定位,重新考虑其作为候选基因的可能性。我们将GM2A定位于5q31.3-q33.1;因此,它不是SMA的候选基因。

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