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编码一种拓扑异构酶I依赖性DNA损伤修复酶的TDP1在伴有轴索性神经病的脊髓小脑共济失调中的突变。

Mutation of TDP1, encoding a topoisomerase I-dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathy.

作者信息

Takashima Hiroshi, Boerkoel Cornelius F, John Joy, Saifi Gulam Mustafa, Salih Mustafa A M, Armstrong Dawna, Mao Yuxin, Quiocho Florante A, Roa Benjamin B, Nakagawa Masanori, Stockton David W, Lupski James R

机构信息

Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USA.

出版信息

Nat Genet. 2002 Oct;32(2):267-72. doi: 10.1038/ng987. Epub 2002 Sep 16.

Abstract

Tyrosyl-DNA phosphodiesterase 1 (TDP1) repairs covalently bound topoisomerase I-DNA complexes and is essential for preventing the formation of double-strand breaks that result when stalled topoisomerase I complexes interfere with DNA replication in yeast. Here we show that a deficiency of this DNA repair pathway in humans does not predispose to neoplasia or dysfunctions in rapidly replicating tissues, but instead causes spinocerebellar ataxia with axonal neuropathy (SCAN1) by affecting large, terminally differentiated, non-dividing neuronal cells. Using genome-wide linkage mapping and a positional candidate approach in a Saudi Arabian family affected with autosomal recessive SCAN1, we identified a homozygous mutation in TDP1 (A1478G) that results in the substitution of histidine 493 with an arginine residue. The His493 residue is conserved in TDP1 across species and is located in the active site of the enzyme. Protein modeling predicts that mutation of this amino acid to arginine will disrupt the symmetric structure of the active site. We propose that loss-of-function mutations in TDP1 may cause SCAN1 either by interfering with DNA transcription or by inducing apoptosis in postmitotic neurons.

摘要

酪氨酰-DNA磷酸二酯酶1(TDP1)可修复共价结合的拓扑异构酶I-DNA复合物,对于防止在酵母中当停滞的拓扑异构酶I复合物干扰DNA复制时产生的双链断裂的形成至关重要。我们在此表明,人类中这种DNA修复途径的缺陷不会使快速复制的组织易患肿瘤或功能障碍,而是通过影响大型、终末分化、不分裂的神经元细胞导致伴轴索性神经病的脊髓小脑共济失调(SCAN1)。利用全基因组连锁图谱分析以及在一个患常染色体隐性SCAN1的沙特阿拉伯家族中采用定位候选方法,我们在TDP1中鉴定出一个纯合突变(A1478G),该突变导致组氨酸493被精氨酸残基取代。His493残基在跨物种的TDP1中保守,且位于该酶的活性位点。蛋白质建模预测该氨基酸突变为精氨酸会破坏活性位点的对称结构。我们提出TDP1中的功能丧失突变可能通过干扰DNA转录或通过诱导有丝分裂后神经元凋亡而导致SCAN1。

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