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卵巢组织转录组分析突出了控制能量平衡和氧化应激的基因,这些基因可能是杂交蛋鸡产蛋数和产蛋量杂种优势的潜在驱动因素。

Transcriptome analysis of ovarian tissues highlights genes controlling energy homeostasis and oxidative stress as potential drivers of heterosis for egg number and clutch size in crossbred laying hens.

机构信息

State Key Laboratory of Animal Biotech Breeding, Key Laboratory of Animal (Poultry) Genetics Breeding and Reproduction, Ministry of Agriculture and Rural Affairs, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China; Department of Animal Science, Usmanu Danfodiyo University, Sokoto, Nigeria.

State Key Laboratory of Animal Biotech Breeding, Key Laboratory of Animal (Poultry) Genetics Breeding and Reproduction, Ministry of Agriculture and Rural Affairs, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China.

出版信息

Poult Sci. 2024 Jan;103(1):103163. doi: 10.1016/j.psj.2023.103163. Epub 2023 Oct 4.

Abstract

Heterosis is the major benefit of crossbreeding and has been exploited in laying hens breeding for a long time. This genetic phenomenon has been linked to various modes of nonadditive gene action. However, the molecular mechanism of heterosis for egg production in laying hens has not been fully elucidated. To fill this research gap, we sequenced mRNAs and lncRNAs of the ovary stroma containing prehierarchical follicles in White Leghorn, Rhode Island Red chickens as well as their reciprocal crossbreds that demonstrated heterosis for egg number and clutch size. We further delineated the modes of mRNAs and lncRNAs expression to identify their potential functions in the observed heterosis. Results showed that dominance was the principal mode of nonadditive expression exhibited by mRNAs and lncRNAs in the prehierarchical follicles of crossbred hens. Specifically, low-parent dominance was the main mode of mRNA expression, while high-parent dominance was the predominant mode of lncRNA expression. Important pathways enriched by genes that showed higher expression in crossbreds compared to either one or both parental lines were cell adhesion molecules, tyrosine and purine metabolism. In contrast, ECM-receptor interaction, focal adhesion, PPAR signaling, and ferroptosis were enriched in genes with lower expression in the crossbred. Protein network interaction identified nonadditively expressed genes including apolipoprotein B (APOB), transferrin, acyl-CoA synthetase medium-chain family member (APOBEC) 3, APOBEC1 complementation factor, and cathepsin S as hub genes. Among these potential hub genes, APOB was the only gene with underdominance expression common to the 2 reciprocal crossbred lines, and has been linked to oxidative stress. LncRNAs with nonadditive expression in the crossbred hens targeted natriuretic peptide receptor 1, epidermal differentiation protein beta, spermatogenesis-associated gene 22, sperm-associated antigen 16, melanocortin 2 receptor, dolichol kinase, glycine amiinotransferase, and prolactin releasing hormone receptor. In conclusion, genes with nonadditive expression in the crossbred may play crucial roles in follicle growth and atresia by improving follicle competence and increasing oxidative stress, respectively. These 2 phenomena could underpin heterosis for egg production in crossbred laying hens.

摘要

杂种优势是杂交的主要优势,长期以来一直被用于蛋鸡的选育。这种遗传现象与各种非加性基因作用模式有关。然而,蛋鸡产蛋杂种优势的分子机制尚未完全阐明。为了填补这一研究空白,我们对怀特莱杭鸡和罗得岛红鸡及其具有产蛋数和总产蛋数杂种优势的正反交杂种母鸡卵巢基质中包含的前层级卵泡进行了 mRNA 和 lncRNA 测序。我们进一步描述了 mRNA 和 lncRNA 表达的模式,以确定它们在观察到的杂种优势中的潜在功能。结果表明,在杂交母鸡的前层级卵泡中,显性是 mRNA 和 lncRNA 非加性表达的主要模式。具体来说,低亲显性是 mRNA 表达的主要模式,而高亲显性是 lncRNA 表达的主要模式。与任一亲本品系或双亲本品系相比,在杂交品系中表达更高的基因富集的重要途径包括细胞黏附分子、酪氨酸和嘌呤代谢。相比之下,在杂交品系中表达较低的基因富集了 ECM-受体相互作用、焦点粘附、PPAR 信号和铁死亡。蛋白质网络互作鉴定出非加性表达的基因,包括载脂蛋白 B(APOB)、转铁蛋白、酰基辅酶 A 合成酶中链家族成员(APOBEC)3、APOBEC1 补体因子和组织蛋白酶 S 作为枢纽基因。在这些潜在的枢纽基因中,APOB 是仅有的在 2 个反向杂交品系中表现出次显性表达的基因,并且与氧化应激有关。在杂交母鸡中具有非加性表达的 lncRNA 靶向利钠肽受体 1、表皮分化蛋白β、精子发生相关基因 22、精子相关抗原 16、黑素皮质素 2 受体、多萜醇激酶、甘氨酸转氨酶和催乳素释放激素受体。总之,在杂交品系中具有非加性表达的基因可能通过提高卵泡的竞争力和增加氧化应激,分别在卵泡生长和闭锁中发挥关键作用。这两个现象可能是杂交蛋鸡产蛋杂种优势的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0274/10684806/855f65b90085/gr1.jpg

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