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牛脊髓性肌萎缩症的精细定位与候选基因分析

Fine-mapping and candidate gene analysis of bovine spinal muscular atrophy.

作者信息

Krebs Stefan, Medugorac Ivica, Russ Ingolf, Ossent Pete, Bleul Ulrich, Schmahl Wolfgang, Förster Martin

机构信息

Faculty of Veterinary Medicine, Institute for Animal Breeding, The Ludwig-Maximilians-University Munich, Veterinaerstrasse 13, 80539 Munich, Germany.

出版信息

Mamm Genome. 2006 Jan;17(1):67-76. doi: 10.1007/s00335-005-0102-3. Epub 2006 Jan 13.

Abstract

Bovine spinal muscular atrophy (SMA), an autosomal recessive neurodegenerative disease, has been mapped at moderate resolution to the distal part of Chromosome 24. In this article we confirm this location and fine-map the SMA locus to an interval of approximately 0.8 cM at the very distal end of BTA24. Despite remarkable similarity to human SMA, the causative gene SMN can be excluded in bovine SMA. However, the interval where the disease now has been mapped contains BCL2, like SMN an antiapoptotic factor, and shown to bind to SMN. Moreover, knockout mice lacking the BCL2 gene show rapid motor neuron degeneration with early postnatal onset, as observed in bovine SMA. A comparative cattle/human map of the distal end of BTA24, based on the emerging bovine genome sequencing data, shows conserved synteny to HSA18 with hints of a segmental duplication and pericentric inversion just after the last available bovine marker DIK4971. This synteny lets us conclude that SMA is in immediate vicinity of the telomere. Candidate gene analysis of BCL2, however, excludes most of this gene, except its promoter region, and draws attention to the neighboring gene VPS4B, part of the endosomal protein-sorting machinery ESCRT-III which is involved in several neurodegenerative diseases.

摘要

牛脊髓性肌萎缩症(SMA)是一种常染色体隐性神经退行性疾病,已以中等分辨率定位到24号染色体的远端。在本文中,我们证实了这一位置,并将SMA基因座精细定位到BTA24最远端约0.8厘摩的区间。尽管与人类SMA有显著相似性,但牛SMA的致病基因SMN可以排除。然而,目前已定位到该疾病的区间包含BCL2,它与SMN一样是一种抗凋亡因子,且已证明可与SMN结合。此外,缺乏BCL2基因的基因敲除小鼠表现出运动神经元快速退化,且在出生后早期发病,这与牛SMA中观察到的情况一样。基于新出现的牛基因组测序数据绘制的BTA24远端的牛/人比较图谱显示,与HSA18存在保守的同线性,在最后一个可用的牛标记DIK4971之后有片段重复和着丝粒周围倒位的迹象。这种同线性使我们得出结论,SMA紧邻端粒。然而,对BCL2的候选基因分析排除了该基因的大部分区域,除了其启动子区域,并将注意力引向了邻近基因VPS4B,它是参与几种神经退行性疾病的内体蛋白分选机制ESCRT-III的一部分。

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