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鉴定胸腺素 β4 为 Hand1 介导的血管发育的效应因子。

Identification of Thymosin β4 as an effector of Hand1-mediated vascular development.

机构信息

Molecular Medicine Unit, UCL-Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK.

出版信息

Nat Commun. 2010 Jul 27;1(4):46. doi: 10.1038/ncomms1041.

Abstract

The bHLH transcription factor Hand1 (Heart and neural crest-derived transcript-1) has a fundamental role in cardiovascular development; however, the molecular mechanisms have not been elucidated. In this paper we identify Thymosin β4 (Tβ4/Tmsb4x), which encodes an actin monomer-binding protein implicated in cell migration and angiogenesis, as a direct target of Hand1. We demonstrate that Hand1 binds an upstream regulatory region proximal to the promoter of Tβ4 at consensus Thing1 and E-Box sites and identify both activation and repression of Tβ4 by Hand1, through direct binding within either non-canonical or canonical E-boxes, providing new insight into gene regulation by bHLH transcription factors. Hand1-mediated activation of Tβ4 is essential for yolk sac vasculogenesis and embryonic survival, and administration of synthetic TB4 partially rescues yolk sac capillary plexus formation in Hand1-null embryos. Thus, we identify an in vivo downstream target of Hand1 and reveal impaired yolk sac vasculogenesis as a primary cause of early embryonic lethality following loss of this critical bHLH factor.

摘要

bHLH 转录因子 Hand1(心脏和神经嵴衍生转录物-1)在心血管发育中具有重要作用;然而,其分子机制尚未阐明。在本文中,我们确定了胸腺素β4(Tβ4/Tmsb4x),它编码一种肌动蛋白单体结合蛋白,参与细胞迁移和血管生成,是 Hand1 的直接靶标。我们证明 Hand1 在 Thing1 和 E-Box 位点结合 Tβ4 启动子上游的调节区域,并通过直接结合非典型或典型 E-Box 来识别 Hand1 对 Tβ4 的激活和抑制,为 bHLH 转录因子的基因调控提供了新的见解。Hand1 介导的 Tβ4 激活对于卵黄囊血管发生和胚胎存活至关重要,并且合成 TB4 的给药部分挽救了 Hand1 缺失胚胎中卵黄囊毛细血管丛的形成。因此,我们确定了 Hand1 的一个体内下游靶标,并揭示了卵黄囊血管生成受损是该关键 bHLH 因子缺失后早期胚胎致死的主要原因。

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