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瘤胃功能创新的遗传适应模式。

Modes of genetic adaptations underlying functional innovations in the rumen.

机构信息

Key Laboratory of Animal Genetics, Breeding and Reproduction of Shaanxi Province, College of Animal Science and Technology, Northwest A&F University, Yangling, 712100, China.

School of Ecology and Environment, Northwestern Polytechnical University, Xi'an, 710072, China.

出版信息

Sci China Life Sci. 2021 Jan;64(1):1-21. doi: 10.1007/s11427-020-1828-8. Epub 2020 Nov 5.

Abstract

The rumen is the hallmark organ of ruminants and hosts a diverse ecosystem of microorganisms that facilitates efficient digestion of plant fibers. We analyzed 897 transcriptomes from three Cetartiodactyla lineages: ruminants, camels and cetaceans, as well as data from ruminant comparative genomics and functional assays to explore the genetic basis of rumen functional innovations. We identified genes with relatively high expression in the rumen, of which many appeared to be recruited from other tissues. These genes show functional enrichment in ketone body metabolism, regulation of microbial community, and epithelium absorption, which are the most prominent biological processes involved in rumen innovations. Several modes of genetic change underlying rumen functional innovations were uncovered, including coding mutations, genes newly evolved, and changes of regulatory elements. We validated that the key ketogenesis rate-limiting gene (HMGCS2) with five ruminant-specific mutations was under positive selection and exhibits higher synthesis activity than those of other mammals. Two newly evolved genes (LYZ1 and DEFB1) are resistant to Gram-positive bacteria and thereby may regulate microbial community equilibrium. Furthermore, we confirmed that the changes of regulatory elements accounted for the majority of rumen gene recruitment. These results greatly improve our understanding of rumen evolution and organ evo-devo in general.

摘要

反刍动物的瘤胃是标志性器官,它拥有一个多样化的微生物生态系统,有助于有效地消化植物纤维。我们分析了三个偶蹄目动物谱系(反刍动物、骆驼和鲸目动物)的 897 个转录组,以及反刍动物比较基因组学和功能分析的数据,以探讨瘤胃功能创新的遗传基础。我们确定了在瘤胃中相对高表达的基因,其中许多似乎是从其他组织招募而来的。这些基因在酮体代谢、微生物群落调节和上皮吸收等方面具有功能富集,这些是与瘤胃创新相关的最显著的生物学过程。我们发现了几种支持瘤胃功能创新的遗传变化模式,包括编码突变、新进化的基因和调控元件的变化。我们验证了具有五个反刍动物特异性突变的关键酮体生成限速基因(HMGCS2)受到正选择,其合成活性高于其他哺乳动物。两个新进化的基因(LYZ1 和 DEFB1)对革兰氏阳性菌具有抗性,因此可能调节微生物群落平衡。此外,我们证实调控元件的变化解释了瘤胃基因招募的大部分原因。这些结果大大提高了我们对瘤胃进化和一般器官进化发育的理解。

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