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Tbx5缓冲内在的左右不对称性,确保前肢对称形成。

Tbx5 Buffers Inherent Left/Right Asymmetry Ensuring Symmetric Forelimb Formation.

作者信息

Sulaiman Fatima A, Nishimoto Satoko, Murphy George R F, Kucharska Anna, Butterfield Natalie C, Newbury-Ecob Ruth, Logan Malcolm P O

机构信息

Division of Developmental Biology, MRC-National Institute for Medical Research, Mill Hill, London, England.

Randall Division of Cell and Molecular Biophysics, King's College London, Guy's Campus, London, England.

出版信息

PLoS Genet. 2016 Dec 19;12(12):e1006521. doi: 10.1371/journal.pgen.1006521. eCollection 2016 Dec.

Abstract

The forelimbs and hindlimbs of vertebrates are bilaterally symmetric. The mechanisms that ensure symmetric limb formation are unknown but they can be disrupted in disease. In Holt-Oram Syndrome (HOS), caused by mutations in TBX5, affected individuals have left-biased upper/forelimb defects. We demonstrate a role for the transcription factor Tbx5 in ensuring the symmetric formation of the left and right forelimb. In our mouse model, bilateral hypomorphic levels of Tbx5 produces asymmetric forelimb defects that are consistently more severe in the left limb than the right, phenocopying the left-biased limb defects seen in HOS patients. In Tbx hypomorphic mutants maintained on an INV mutant background, with situs inversus, the laterality of defects is reversed. Our data demonstrate an early, inherent asymmetry in the left and right limb-forming regions and that threshold levels of Tbx5 are required to overcome this asymmetry to ensure symmetric forelimb formation.

摘要

脊椎动物的前肢和后肢呈双侧对称。确保肢体对称形成的机制尚不清楚,但在疾病中可能会被破坏。在由TBX5突变引起的霍尔特-奥勒姆综合征(HOS)中,受影响的个体存在左偏的上肢/前肢缺陷。我们证明了转录因子Tbx5在确保左右前肢对称形成中的作用。在我们的小鼠模型中,Tbx5的双侧亚效等位基因水平会产生不对称的前肢缺陷,且左肢的缺陷始终比右肢更严重,这模拟了HOS患者中出现的左偏肢体缺陷。在维持在INV突变背景下且有内脏反位的Tbx亚效等位基因突变体中,缺陷的偏向性会反转。我们的数据表明,左右肢体形成区域存在早期的内在不对称性,并且需要Tbx5的阈值水平来克服这种不对称性,以确保前肢对称形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b24/5215935/ac718f2c3b42/pgen.1006521.g001.jpg

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