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Delineating a Conserved Genetic Cassette Promoting Outgrowth of Body Appendages

机译:划定一个保守的基因盒带动身体附件的生长

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摘要

The acquisition of the external genitalia allowed mammals to cope with terrestrial-specific reproductive needs for internal fertilization, and thus it represents one of the most fundamental steps in evolution towards a life on land. How genitalia evolved remains obscure, and the key to understanding this process may lie in the developmental genetics that underpins the early establishment of the genital primordium, the genital tubercle (GT). Development of the GT is similar to that of the limb, which requires precise regulation from a distal signaling epithelium. However, whether outgrowth of the GT and limbs is mediated by common instructive signals remains unknown. In this study, we used comprehensive genetic approaches to interrogate the signaling cascade involved in GT formation in comparison with limb formation. We demonstrate that the FGF ligand responsible for GT development is FGF8 expressed in the cloacal endoderm. We further showed that forced Fgf8 expression can rescue limb and GT reduction in embryos deficient in WNT signaling activity. Our studies show that the regulation of Fgf8 by the canonical WNT signaling pathway is mediated in part by the transcription factor SP8. Sp8 mutants elicit appendage defects mirroring WNT and FGF mutants, and abolishing Sp8 attenuates ectopic appendage development caused by a gain-of-function β-catenin mutation. These observations indicate that a conserved WNT-SP8-FGF8 genetic cassette is employed by both appendages for promoting outgrowth, and suggest a deep homology shared by the limb and external genitalia.
机译:外部生殖器的获得使哺乳动物能够应对陆地特定的内部受精生殖需求,因此,它代表着向陆上生物发展的最基本步骤之一。生殖器如何进化仍然不清楚,理解这一过程的关键可能在于发育遗传学,该遗传学支持生殖器原基(生殖器结节,GT)的早期建立。 GT的发展与肢体的发展相似,这需要远端信号上皮的精确调控。但是,GT和四肢的长大是否由常见的指导性信号介导仍是未知的。在这项研究中,我们使用综合的遗传学方法来询问与肢体形成相比,GT形成中涉及的信号级联。我们证明负责GT发展的FGF配体是泄殖腔内胚层中表达的FGF8。我们进一步表明,强迫性Fgf8表达可以挽救WNT信号活性不足的胚胎的肢体和GT减少。我们的研究表明,经典WNT信号通路对Fgf8的调节部分由转录因子SP8介导。 Sp8突变体引起与WNT和FGF突变体相似的附件缺陷,而废除Sp8则减弱了由功能获得性β-catenin突变引起的异位附件发育。这些观察结果表明,两个附肢都采用保守的WNT-SP8-FGF8遗传盒来促进生长,并表明肢体和外生殖器共有很深的同源性。

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