Transcriptome analysis reveals the key long non-coding RNAs and genes related to cashmere shedding in goats.

IF 2.5 2区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Yixing Fan, Tiantian Gong, Siyu Feng, Huiling Zhang, Ran Wang, Mingzhao Hu, Qi Zhang, Taiyu Hui, Jincheng Shen, Ruqing Xu, Yubo Zhu, Man Bai, Zeying Wang, Wenlin Bai
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引用次数: 0

Abstract

Objective: Cashmere goat is renowned for its superior characteristics of cashmere fibers. Cashmere shedding is closely related to the cashmere production in cashmere goats, but its molecular regulatory mechanism is not fully understood.

Methods: In this study, we collected skin tissues from already-shed cashmere goats (AS) and non-shed cashmere goats (NS). Morphological differences were observed and relative expression levels of indicator genes distinguishing anagen from telogen of hair follicles were assessed. Whole transcriptome sequencing was employed to investigate key regulatory factors including long non-coding RNAs (lncRNAs) and different expression genes (DEGs) and followed by preliminary validation, interaction network construction and functional verification.

Results: Comparative histological analysis found that density, depth, width, hair bulb width and activity of secondary hair follicles (SHFs) in AS individuals were significantly lower than those in NS individuals. Expression detection results of indicator genes distinguishing anagen from telogen indicated that the SHFs of NS individuals were predominantly in telogen phase, whereas those of AS individuals were more inclined towards anagen phase. Transcriptome sequencing analysis screened 450 DEGs with 338 upregulated and 112 downregulated, as well as 352 different expression lncRNAs including 168 upregulated and 184 downregulated. Regulatory networks of lncRNAs and their co-expression DEGs were constructed, and lncRNA LOC108637151 and its co-expression gene, Selenoprotein P (SEPP1), were identified as key regulatory factors of cashmere shedding in goats, and both of them showed high expression levels in AS individuals. The overexpression of LOC108637151 in dermal papilla cells (DPCs) led to the increasing expression of its target gene SEPP1 and promoted the proliferation of DPCs in cashmere goats.

Conclusion: This study identified key lncRNAs and genes related to cashmere shedding in goats along with their regulatory relationships. The results provided a basis for revealing the potential molecular mechanisms of cashmere shedding in goats.

转录组分析揭示了山羊羊绒脱落的关键长链非编码rna和相关基因。
目的:羊绒山羊以其优越的羊绒纤维特性而闻名。绒山羊的脱绒与羊绒产量密切相关,但其分子调控机制尚不完全清楚。方法:本研究采集已蜕绒山羊(AS)和未蜕绒山羊(NS)的皮肤组织。观察毛囊生长和休止期的形态学差异,并评估毛囊生长和休止期指示基因的相对表达水平。采用全转录组测序技术研究长链非编码rna (long non-coding rna, lncRNAs)和不同表达基因(different expression genes, DEGs)等关键调控因子,并进行初步验证、相互作用网络构建和功能验证。结果:比较组织学分析发现,AS个体的次毛囊(SHFs)密度、深度、宽度、毛球宽度和活性显著低于NS个体。生长休止期与休止期区分指示基因的表达检测结果表明,NS个体的SHFs主要处于休止期,而AS个体的SHFs更倾向于生长休止期。转录组测序分析筛选出450个deg,其中338个表达上调,112个表达下调;352个不同表达的lncrna,其中168个表达上调,184个表达下调。构建lncRNA及其共表达基因deg调控网络,确定lncRNA LOC108637151及其共表达基因硒蛋白P (SEPP1)是山羊脱绒的关键调控因子,且两者在as个体中均表现出高表达水平。LOC108637151在绒山羊真皮乳头细胞(DPCs)中过表达,导致其靶基因SEPP1表达增加,促进了DPCs在绒山羊体内的增殖。结论:本研究确定了山羊羊绒脱落相关的关键lncrna和基因,以及它们之间的调控关系。研究结果为揭示山羊脱绒的潜在分子机制提供了基础。
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来源期刊
Animal Bioscience
Animal Bioscience AGRICULTURE, DAIRY & ANIMAL SCIENCE-
CiteScore
5.00
自引率
0.00%
发文量
223
审稿时长
3 months
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