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嘌呤稳态对于 中的发育定时、生殖系维持和肌肉完整性是必要的。

Purine Homeostasis Is Necessary for Developmental Timing, Germline Maintenance and Muscle Integrity in .

机构信息

Institut de Biochimie et Génétique Cellulaires, Université de Bordeaux and CNRS UMR5095, 33077 Bordeaux cedex, France.

Andalusian Center for Developmental Biology, Consejo Superior de Investigaciones Científicas/Junta de Andalucía/Universidad Pablo de Olavide, Department of Molecular Biology and Biochemical Engineering, 41013 Seville, Spain.

出版信息

Genetics. 2019 Apr;211(4):1297-1313. doi: 10.1534/genetics.118.301062. Epub 2019 Jan 30.

Abstract

Purine homeostasis is ensured through a metabolic network widely conserved from prokaryotes to humans. Purines can either be synthesized , reused, or produced by interconversion of extant metabolites using the so-called recycling pathway. Although thoroughly characterized in microorganisms, such as yeast or bacteria, little is known about regulation of the purine biosynthesis network in metazoans. In humans, several diseases are linked to purine metabolism through as yet poorly understood etiologies. Particularly, the deficiency in adenylosuccinate lyase (ADSL)-an enzyme involved both in the purine and recycling pathways-causes severe muscular and neuronal symptoms. In order to address the mechanisms underlying this deficiency, we established as a metazoan model organism to study purine metabolism, while focusing on ADSL. We show that the purine biosynthesis network is functionally conserved in Moreover, (the gene encoding ADSL in ) is required for developmental timing, germline stem cell maintenance and muscle integrity. Importantly, these traits are not affected when solely the pathway is abolished, and we present evidence that germline maintenance is linked specifically to ADSL activity in the recycling pathway. Hence, our results allow developmental and tissue specific phenotypes to be ascribed to separable steps of the purine metabolic network in an animal model.

摘要

嘌呤稳态是通过一个广泛存在于原核生物到人类的代谢网络来保证的。嘌呤可以通过合成、再利用或现存代谢物的相互转化来产生,这就是所谓的回收途径。尽管在微生物(如酵母或细菌)中得到了充分的研究,但人们对真核生物嘌呤生物合成网络的调控知之甚少。在人类中,有几种疾病与嘌呤代谢有关,其病因尚不清楚。特别是,腺嘌呤琥珀酸裂解酶(ADSL)——一种既参与嘌呤途径又参与回收途径的酶的缺乏,会导致严重的肌肉和神经元症状。为了研究这种缺乏的机制,我们建立了一个真核生物模型生物来研究嘌呤代谢,同时重点研究 ADSL。我们发现,嘌呤生物合成网络在功能上是保守的,此外,(编码 ADSL 的基因)对于发育时间、生殖干细胞维持和肌肉完整性是必需的。重要的是,当仅仅废除 途径时,这些特征不受影响,我们提供的证据表明,生殖干细胞的维持与回收途径中 ADSL 活性特异性相关。因此,我们的结果允许在动物模型中将可分离的嘌呤代谢网络步骤归因于发育和组织特异性表型。

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