Suppr超能文献

小尾寒羊与杜泊×小尾寒羊杂交羊背最长肌全基因组DNA甲基化的比较分析

Comparative analysis on genome-wide DNA methylation in longissimus dorsi muscle between Small Tailed Han and Dorper×Small Tailed Han crossbred sheep.

作者信息

Cao Yang, Jin Hai-Guo, Ma Hui-Hai, Zhao Zhi-Hui

机构信息

College of Animal Science, Jilin University, Changchun 130012, China.

Branch of Animal Husbandry, Jilin Academy of Agricultural Sciences, Changchun 130033, China.

出版信息

Asian-Australas J Anim Sci. 2017 Nov;30(11):1529-1539. doi: 10.5713/ajas.17.0154. Epub 2017 Jun 27.

Abstract

OBJECTIVE

The objective of this study was to compare the DNA methylation profile in the longissimus dorsi muscle between Small Tailed Han and Dorper×Small Tailed Han crossbred sheep which were known to exhibit significant difference in meat-production.

METHODS

Six samples (three in each group) were subjected to the methylated DNA immunoprecipitation sequencing (MeDIP-seq) and subsequent bioinformatics analyses to detect differentially methylated regions (DMRs) between the two groups.

RESULTS

23.08 Gb clean data from six samples were generated and 808 DMRs were identified in gene body or their neighboring up/downstream regions. Compared with Small Tailed Han sheep, we observed a tendency toward a global loss of DNA methylation in these DMRs in the crossbred group. Gene ontology enrichment analysis found several gene sets which were hypo-methylated in gene-body region, including nucleoside binding, motor activity, phospholipid binding and cell junction. Numerous genes were found to be differentially methylated between the two groups with several genes significantly differentially methylated, including transforming growth factor beta 3 (TGFB3), acyl-CoA synthetase long chain family member 1 (ACSL1), ryanodine receptor 1 (RYR1), acyl-CoA oxidase 2 (ACOX2), peroxisome proliferator activated receptor-gamma2 (PPARG2), netrin 1 (NTN1), ras and rab interactor 2 (RIN2), microtubule associated protein RP/EB family member 1 (MAPRE1), ADAM metallopeptidase with thrombospondin type 1 motif 2 (ADAMTS2), myomesin 1 (MYOM1), zinc finger, DHHC type containing 13 (ZDHHC13), and SH3 and PX domains 2B (SH3PXD2B). The real-time quantitative polymerase chain reaction validation showed that the 12 genes are differentially expressed between the two groups.

CONCLUSION

In the current study, a tendency to a global loss of DNA methylation in these DMRs in the crossbred group was found. Twelve genes, TGFB3, ACSL1, RYR1, ACOX2, PPARG2, NTN1, RIN2, MAPRE1, ADAMTS2, MYOM1, ZDHHC13, and SH3PXD2B, were found to be differentially methylated between the two groups by gene ontology enrichment analysis. There are differences in the expression of 12 genes, of which ACSL1, RIN2, and ADAMTS2 have a negative correlation with methylation levels and the data suggest that DNA methylation levels in DMRs of the 3 genes may have an influence on the expression. These results will serve as a valuable resource for DNA methylation investigations on screening candidate genes which might be related to meat production in sheep.

摘要

目的

本研究旨在比较小尾寒羊和杜泊×小尾寒羊杂交羊背最长肌中的DNA甲基化谱,已知这两种羊在产肉性能上存在显著差异。

方法

对六个样本(每组三个)进行甲基化DNA免疫沉淀测序(MeDIP-seq)及后续生物信息学分析,以检测两组之间的差异甲基化区域(DMR)。

结果

六个样本共产生23.08 Gb的clean数据,在基因体或其相邻的上下游区域鉴定出808个DMR。与小尾寒羊相比,杂交组中这些DMR的DNA甲基化呈现整体丢失的趋势。基因本体富集分析发现了几个在基因体区域低甲基化的基因集,包括核苷结合、运动活性、磷脂结合和细胞连接。发现两组之间有许多基因存在差异甲基化,其中几个基因差异显著,包括转化生长因子β3(TGFB3)、酰基辅酶A合成酶长链家族成员1(ACSL1)、兰尼碱受体1(RYR1)、酰基辅酶A氧化酶2(ACOX2)、过氧化物酶体增殖物激活受体γ2(PPARG2)、网蛋白1(NTN1)、Ras和Rab相互作用蛋白2(RIN2)、微管相关蛋白RP/EB家族成员1(MAPRE1)、含血小板反应蛋白基序的金属蛋白酶2(ADAMTS2)、肌间蛋白1(MYOM1)、含DHHC型锌指蛋白13(ZDHHC13)以及SH3和PX结构域2B(SH3PXD2B)。实时定量聚合酶链反应验证表明,这12个基因在两组之间差异表达。

结论

在本研究中,发现杂交组中这些DMR的DNA甲基化呈现整体丢失的趋势。通过基因本体富集分析发现,TGFB3、ACSL1、RYR1、ACOX2、PPARG2、NTN1、RIN2、MAPRE1、ADAMTS2、MYOM1、ZDHHC13和SH3PXD2B这12个基因在两组之间存在差异甲基化。12个基因的表达存在差异,其中ACSL1、RIN2和ADAMTS2与甲基化水平呈负相关,数据表明这3个基因DMR中的DNA甲基化水平可能对表达有影响。这些结果将为筛选可能与绵羊产肉性能相关的候选基因的DNA甲基化研究提供有价值的资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bc4/5666187/fd856a9d64a0/ajas-30-11-1529f1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验