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Structural and biochemical basis for the inhibition of cell death by APIP, a methionine salvage enzyme.APIP,一种甲硫氨酸补救酶,其抑制细胞死亡的结构和生化基础。
Proc Natl Acad Sci U S A. 2014 Jan 7;111(1):E54-61. doi: 10.1073/pnas.1308768111. Epub 2013 Dec 23.
2
A cellular genome-wide association study reveals human variation in microtubule stability and a role in inflammatory cell death.一项细胞全基因组关联研究揭示了人类微管稳定性的变异与炎症细胞死亡的关系。
Mol Biol Cell. 2014 Jan;25(1):76-86. doi: 10.1091/mbc.E13-06-0294. Epub 2013 Oct 30.
3
Understanding human variation in infectious disease susceptibility through clinical and cellular GWAS.通过临床和细胞全基因组关联研究了解人类在传染病易感性方面的差异。
PLoS Pathog. 2013;9(8):e1003424. doi: 10.1371/journal.ppat.1003424. Epub 2013 Aug 1.
4
Microtubule-based transport - basic mechanisms, traffic rules and role in neurological pathogenesis.基于微管的运输-基本机制、交通规则及其在神经发病机制中的作用。
J Cell Sci. 2013 Jun 1;126(Pt 11):2319-29. doi: 10.1242/jcs.115030. Epub 2013 May 31.
5
β-Tubulin mutations that cause severe neuropathies disrupt axonal transport.导致严重神经病变的β-微管蛋白突变会破坏轴突运输。
EMBO J. 2013 May 15;32(10):1352-64. doi: 10.1038/emboj.2013.59. Epub 2013 Mar 15.
6
Overlapping cortical malformations and mutations in TUBB2B and TUBA1A.TUBB2B 和 TUBA1A 中皮层发育不良和突变的重叠。
Brain. 2013 Feb;136(Pt 2):536-48. doi: 10.1093/brain/aws338. Epub 2013 Jan 29.
7
Functional identification of APIP as human mtnB, a key enzyme in the methionine salvage pathway.鉴定 APIP 为人源 mtnB,甲硫氨酸补救途径中的关键酶。
PLoS One. 2012;7(12):e52877. doi: 10.1371/journal.pone.0052877. Epub 2012 Dec 28.
8
Functional genetic screen of human diversity reveals that a methionine salvage enzyme regulates inflammatory cell death.人类多样性的功能遗传筛选揭示了一种蛋氨酸回收酶调节炎症细胞死亡。
Proc Natl Acad Sci U S A. 2012 Aug 28;109(35):E2343-52. doi: 10.1073/pnas.1206701109. Epub 2012 Jul 25.
9
Patterns of cis regulatory variation in diverse human populations.不同人类群体中顺式调控变异的模式。
PLoS Genet. 2012;8(4):e1002639. doi: 10.1371/journal.pgen.1002639. Epub 2012 Apr 19.
10
Whole-genome studies identify solute carrier transporters in cellular susceptibility to paclitaxel.全基因组研究鉴定出细胞对紫杉醇敏感性的溶质载体转运蛋白。
Pharmacogenet Genomics. 2012 Jul;22(7):498-507. doi: 10.1097/FPC.0b013e328352f436.

数量遗传学与细胞生物学的结合:一种新型筛选方法揭示人类在微管稳定性方面存在基因编码变异。

The marriage of quantitative genetics and cell biology: a novel screening approach reveals people have genetically encoded variation in microtubule stability.

作者信息

Ko Dennis C, Jaslow Sarah L

机构信息

Department of Molecular Genetics and Microbiology; School of Medicine; Duke University; Durham, NC USA; Department of Medicine and the Center for Human Genome Variation; School of Medicine; Duke University; Durham, NC USA.

Department of Molecular Genetics and Microbiology; School of Medicine; Duke University; Durham, NC USA.

出版信息

Bioarchitecture. 2014 Mar-Apr;4(2):58-61. doi: 10.4161/bioa.28481. Epub 2014 Mar 11.

DOI:10.4161/bioa.28481
PMID:24618686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4199813/
Abstract

Microtubules play a central role in many essential cellular processes, including chromosome segregation, intracellular transport, and cell polarity. As these dynamic polymers are crucial components of eukaryotic cellular architecture, we were surprised by our recent discovery that a common human genetic difference leads to variation in microtubule stability in cells from different people. A single nucleotide polymorphism (SNP) near the TUBB6 gene, encoding class V β-tubulin, is associated with the expression level of this protein, which reduces microtubule stability at higher levels of expression. We discuss the novel cellular GWAS (genome-wide association study) platform that led to this discovery of natural, common variation in microtubule stability and the implications this finding may have for human health and disease, including cancer and neurological disorders. Furthermore, our generalizable approach provides a gateway for cell biologists to help interpret the functional consequences of human genetic variation.

摘要

微管在许多重要的细胞过程中发挥着核心作用,包括染色体分离、细胞内运输和细胞极性。由于这些动态聚合物是真核细胞结构的关键组成部分,我们最近发现一个常见的人类基因差异会导致不同人细胞中微管稳定性的变化,这让我们感到惊讶。编码V类β-微管蛋白的TUBB6基因附近的一个单核苷酸多态性(SNP)与该蛋白的表达水平相关,在较高表达水平时会降低微管稳定性。我们讨论了导致这一微管稳定性自然常见变异发现的新型细胞全基因组关联研究(GWAS)平台,以及这一发现可能对人类健康和疾病(包括癌症和神经疾病)产生的影响。此外,我们的通用方法为细胞生物学家帮助解释人类基因变异的功能后果提供了一条途径。