全转录组分析揭示了非编码RNA调控抱窝母鸡卵巢萎缩的调控网络及相关通路。

Whole transcriptome analysis revealed the regulatory network and related pathways of non-coding RNA regulating ovarian atrophy in broody hens.

作者信息

Xiong Hanlin, Li Wendong, Wang Lecong, Wang Xuchen, Tang Bincheng, Cui Zhifu, Liu Lingbin

机构信息

College of Animal Science and Technology, Southwest University, Chongqing, China.

出版信息

Front Vet Sci. 2024 May 29;11:1399776. doi: 10.3389/fvets.2024.1399776. eCollection 2024.

Abstract

Poultry broodiness can cause ovarian atresia, which has a detrimental impact on egg production. Non-coding RNAs (ncRNAs) have become one of the most talked-about topics in life sciences because of the increasing evidence of their novel biological roles in regulatory systems. However, the molecular mechanisms of ncRNAs functions and processes in chicken ovarian development remain largely unknown. Whole-transcriptome RNA sequencing of the ovaries of broodiness and laying chickens was thus performed to identify the ncRNA regulatory mechanisms associated with ovarian atresia in chickens. Subsequent analysis revealed that the ovaries of laying chickens and those with broodiness had 40 differentially expressed MicroRNA (miRNAs) (15 up-regulated and 25 down-regulated), 379 differentially expressed Long Noncoding RNA (lncRNAs) (213 up-regulated and 166 down-regulated), and 129 differentially expressed circular RNA (circRNAs) (63 up-regulated and 66 down-regulated). The competing endogenous RNAs (ceRNA) network analysis further revealed the involvement of ECM-receptor interaction, AGE-RAGE signaling pathway, focal adhesion, cytokine-cytokine receptor interaction, inflammatory mediator regulation of TRP channels, renin secretion, gap junction, insulin secretion, serotonergic synapse, and IL-17 signaling pathways in broodiness. Upon further analysis, it became evident that and are significant candidate genes implicated in the regulation of broodiness. The expression of these genes is linked to miR-155-x, miR-211-z, miR-1682-z, gga-miR-155, and gga-miR-1682, as well as to the competitive binding of novel_circ_014674 and MSTRG.3306.4. The findings of this study reveal the existence of a regulatory link between non-coding RNAs and their competing mRNAs, which provide a better comprehension of the ncRNA function and processes in chicken ovarian development.

摘要

家禽抱窝会导致卵巢闭锁,这对产蛋量有不利影响。非编码RNA(ncRNAs)因其在调控系统中新型生物学作用的证据不断增加,已成为生命科学中最受关注的话题之一。然而,ncRNAs在鸡卵巢发育中的功能和作用机制仍 largely unknown。因此,对抱窝鸡和产蛋鸡的卵巢进行了全转录组RNA测序,以确定与鸡卵巢闭锁相关的ncRNA调控机制。随后的分析表明,产蛋鸡和抱窝鸡的卵巢有40个差异表达的微小RNA(miRNAs)(15个上调和25个下调)、379个差异表达的长链非编码RNA(lncRNAs)(213个上调和166个下调)以及129个差异表达的环状RNA(circRNAs)(63个上调和66个下调)。竞争性内源RNA(ceRNA)网络分析进一步揭示了细胞外基质-受体相互作用、晚期糖基化终产物受体(AGE-RAGE)信号通路、粘着斑、细胞因子-细胞因子受体相互作用、TRP通道的炎症介质调节、肾素分泌、缝隙连接、胰岛素分泌、5-羟色胺能突触和IL-17信号通路参与抱窝过程。进一步分析发现, 和 是参与抱窝调控的重要候选基因。这些基因的表达与miR-155-x、miR-211-z、miR-1682-z、gga-miR-155和gga-miR-1682以及novel_circ_014674和MSTRG.3306.4的竞争性结合有关。本研究结果揭示了非编码RNA与其竞争性mRNA之间存在调控联系,这有助于更好地理解ncRNAs在鸡卵巢发育中的功能和作用机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b0b/11168117/11e99d64d655/fvets-11-1399776-g001.jpg

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