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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.

DOI:10.1007/s00335-005-0102-3
PMID:16416092
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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本文引用的文献

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Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia.额颞叶痴呆中内体ESCRTIII复合物亚基CHMP2B的突变。
Nat Genet. 2005 Aug;37(8):806-8. doi: 10.1038/ng1609. Epub 2005 Jul 24.
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PHLPP: a phosphatase that directly dephosphorylates Akt, promotes apoptosis, and suppresses tumor growth.PHLPP:一种直接使Akt去磷酸化、促进细胞凋亡并抑制肿瘤生长的磷酸酶。
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A comprehensive radiation hybrid map of the bovine genome comprising 5593 loci.
3-酮二氢鞘氨醇还原酶FVT1中的一个错义突变作为牛脊髓性肌萎缩症的候选致病突变。
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一张包含5593个位点的牛基因组综合辐射杂种图谱。
Genomics. 2005 Apr;85(4):413-24. doi: 10.1016/j.ygeno.2004.12.007.
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The hereditary spastic paraplegia protein spastin interacts with the ESCRT-III complex-associated endosomal protein CHMP1B.遗传性痉挛性截瘫蛋白spastin与ESCRT-III复合物相关的内体蛋白CHMP1B相互作用。
Hum Mol Genet. 2005 Jan 1;14(1):19-38. doi: 10.1093/hmg/ddi003. Epub 2004 Nov 10.
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A comprehensive genetic map of the cattle genome based on 3802 microsatellites.基于3802个微卫星构建的牛基因组综合遗传图谱。
Genome Res. 2004 Oct;14(10A):1987-98. doi: 10.1101/gr.2741704.
6
Amyotrophic lateral sclerosis-associated SOD1 mutant proteins bind and aggregate with Bcl-2 in spinal cord mitochondria.肌萎缩侧索硬化症相关的超氧化物歧化酶1突变蛋白与脊髓线粒体中的Bcl-2结合并聚集。
Neuron. 2004 Jul 8;43(1):19-30. doi: 10.1016/j.neuron.2004.06.021.
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A first generation bovine BAC-based physical map.第一代基于牛细菌人工染色体的物理图谱。
Genet Sel Evol. 2004 Jan-Feb;36(1):105-22. doi: 10.1186/1297-9686-36-1-105.
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A cattle-human comparative map built with cattle BAC-ends and human genome sequence.利用牛细菌人工染色体(BAC)末端和人类基因组序列构建的牛-人类比较图谱。
Genome Res. 2003 Aug;13(8):1966-72. doi: 10.1101/gr.1560203.
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