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Regulation of nodal and BMP signaling by tomoregulin-1 (X7365) through novel mechanisms

机译:tomoregulin-1(X7365)通过新机制调节淋巴结和BMP信号传导

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During early vertebrate development, members of the transforming growth factor beta (TGFbeta) family play important roles in a variety of processes, including germ layer specification, patterning, cell differentiation, migration, and organogenesis. The activities of TGFbetas need to be tightly controlled to ensure their function at the right time and place. Despite identification of multiple regulators of Bone Morphogenetic Protein (BMP) subfamily ligands, modulators of the activinodal class of TGFbeta ligands are limited, and include follistatin, Cerberus, and Lefty. Recently, a membrane protein, tomoregulin-1 (TMEFF1, originally named X7365), was isolated and found to contain two follistatin modules in addition to an Epidermal Growth Factor (EGF) domain, suggesting that TMEFF1 may participate in regulation of TGFbeta function. Here, we show that, unlike follistatin and follistatin-related gene (FLRG), TMEFF1 inhibits nodal but not activin in Xenopus. Interestingly, both the follistatin modules and the EGF motif contribute to nodal inhibition. A soluble protein containing the follistatin and the EGF domains, however, is not sufficient for nodal inhibition; the location of TMEFF1 at the membrane is essential for its function. These results suggest that TMEFF1 inhibits nodal through a novel mechanism. TMEFF1 also blocks mesodermal, but not epidermal induction by BMP2. Unlike nodal inhibition, regulation of BMP activities by TMEFF1 requires the latter's cytoplasmic tail, while deletion of either the follistatin modules or the EGF motif does not interfere with the BMP inhibitory function of TMEFF1. These results imply that TMEFF1 may employ different mechanisms in the regulation of nodal and BMP signals. In Xenopus, TMEFF1 is expressed from midgastrula stages onward and is enriched in neural tissue derivatives. This expression pattern suggests that TMEFF1 may modulate nodal and BMP activities during neural patterning. In summary, our data demonstrate that tomoregulin-1 is a novel regulator of nodal and BMP signaling during early vertebrate embryogenesis. (C) 2003 Elsevier Science (USA). All rights reserved. [References: 57]
机译:在早期脊椎动物发育过程中,转化生长因子β(TGFbeta)家族的成员在多种过程中起着重要作用,包括胚层规格,模式,细胞分化,迁移和器官发生。需要严格控制TGFbetas的活动,以确保其在正确的时间和地点发挥作用。尽管鉴定了骨形态发生蛋白(BMP)亚家族配体的多种调节剂,但TGFβ配体的激活素/节点类的调节剂仍然有限,包括卵泡抑素,Cerberus和Lefty。最近,分离了一种膜蛋白tomoregulin-1(TMEFF1,最初命名为X7365),发现它除了表皮生长因子(EGF)结构域外还包含两个卵泡抑素模块,表明TMEFF1可能参与了TGFbeta功能的调节。在这里,我们显示,与卵泡抑素和卵泡抑素相关基因(FLRG)不同,TMEFF1在非洲爪蟾中抑制淋巴结但不抑制激活素。有趣的是,卵泡抑素模块和EGF基序均有助于抑制淋巴结。但是,含有卵泡抑素和EGF结构域的可溶性蛋白不足以抑制淋巴结。 TMEFF1在膜上的位置对其功能至关重要。这些结果表明TMEFF1通过一种新颖的机制抑制节点。 TMEFF1还阻止BMP2诱导中胚层,但不阻止表皮诱导。与淋巴结抑制不同,TMEFF1对BMP活性的调节需要后者的胞质尾巴,而卵泡抑素模块或EGF基序的缺失则不会干扰TMEFF1的BMP抑制功能。这些结果表明,TMEFF1在节点和BMP信号的调节中可能采用不同的机制。在非洲爪蟾中,TMEFF1从胃中部开始表达,并富含神经组织衍生物。此表达模式表明TMEFF1可能在神经模式形成过程中调节淋巴结和BMP活性。总之,我们的数据表明tomoregulin-1是早期脊椎动物胚胎发生过程中新型的节点和BMP信号调节剂。 (C)2003 Elsevier Science(美国)。版权所有。 [参考:57]

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