TDP-43 in central nervous system development and function: clues to TDP-43-associated neurodegeneration

被引:65
作者
Sephton, Chantelle F. [1 ]
Cenik, Basar [1 ,3 ]
Cenik, Bercin Kutluk [2 ]
Herz, Joachim [3 ]
Yu, Gang [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Neurosci, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Hamon Ctr Therapeut Oncol Res, Dallas, TX 75390 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Mol Genet, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
amyotrophic lateral sclerosis (ALS); neural development; PTPB2; RIP-seq; RNA binding protein; TDP-43; AMYOTROPHIC-LATERAL-SCLEROSIS; FRONTOTEMPORAL LOBAR DEGENERATION; DNA-BINDING PROTEIN; NUCLEAR FACTOR TDP-43; MESSENGER-RNA; TRANSGENIC MICE; MOTOR DEFICITS; CFTR EXON-9; IN-VIVO; ALS;
D O I
10.1515/hsz-2012-0115
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
From the earliest stages of embryogenesis and throughout life, transcriptional regulation is carefully orchestrated in order to generate, shape, and reshape the central nervous system (CNS). TAR DNA-binding protein 43 (TDP-43) is identified as a regulator of essential transcriptional events in the CNS. Evidence for its importance comes from the identification of TDP-43 protein aggregates and genetic mutations in patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration. Efforts are being made to learn more about the biological function of TDP-43 and gain a better understanding of its role in neurodegeneration. TDP-43 RNA targets and protein interactions have now been identified, and in vivo evidence shows that TDP-43 is essential in CNS development and function. This review will highlight aspects of these findings.
引用
收藏
页码:589 / 594
页数:6
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