Whole-transcriptome splicing profiling of E7.5 mouse primary germ layers reveals frequent alternative promoter usage during mouse early embryogenesis
Whole-transcriptome splicing profiling of E7.5 mouse primary germ layers reveals frequent alternative promoter usage during mouse early embryogenesis
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E7.5小鼠初级胚层的全转录组剪接分析揭示了小鼠早期胚胎发生过程中频繁使用的替代启动子
DOI:
10.1242/bio.032508
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发表时间:
2018-03
期刊:
影响因子:
2.4
通讯作者:
Li Lei
中科院分区:
文献类型:
--
作者:
Lu Xukun;Zhao Zhen-Ao;Wang Xiaoqing;Zhang Xiaoxin;Zhai Yanhua;Deng Wenbo;Yi Zhaohong;Li Lei
ABSTRACT Alternative splicing (AS) and alternative promoter (AP) usage expand the repertories of mammalian transcriptome profiles and thus diversify gene functions. However, our knowledge about the extent and functions of AS and AP usage in mouse early embryogenesis remains elusive. Here, by performing whole-transcriptome splicing profiling with high-throughput next generation sequencing, we report that AS extensively occurs in embryonic day (E) 7.5 mouse primary germ layers, and may be involved in multiple developmental processes. In addition, numerous RNA splicing factors are differentially expressed and alternatively spliced across the three germ layers, implying the potential importance of AS machinery in shaping early embryogenesis. Notably, AP usage is remarkably frequent at this stage, accounting for more than one quarter (430/1,648) of the total significantly different AS events. Genes generating the 430 AP events participate in numerous biological processes, and include important regulators essential for mouse early embryogenesis, suggesting that AP usage is widely used and might be relevant to mouse germ layer specification. Our data underline the potential significance of AP usage in mouse gastrulation, providing a rich data source and opening another dimension for understanding the regulatory mechanisms of mammalian early development. Summary: This study seeks to capture the alternative splicing landscape during mouse gastrulation, underlining the potential importance of alternative promoter usage in mammalian early embryogenesis.
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影响因子:
64.8
作者:
Heintzman, Nathaniel D.;Hon, Gary C.;Hawkins, R. David;Kheradpour, Pouya;Stark, Alexander;Harp, Lindsey F.;Ye, Zhen;Lee, Leonard K.;Stuart, Rhona K.;Ching, Christina W.;Ching, Keith A.;Antosiewicz-Bourget, Jessica E.;Liu, Hui;Zhang, Xinmin;Green, Roland D.;Lobanenkov, Victor V.;Stewart, Ron;Thomson, James A.;Crawford, Gregory E.;Kellis, Manolis;Ren, Bing
通讯作者:
Ren, Bing
影响因子:
14.9
作者:
通讯作者:
--
影响因子:
4.6
作者:
Verdier-Pinard P;Salaun D;Bouguenina H;Shimada S;Pophillat M;Audebert S;Agavnian E;Coslet S;Charafe-Jauffret E;Tachibana T;Badache A
通讯作者:
Badache A
DOI:
10.1083/jcb.200712086
发表时间:
2008-09-22
期刊:
The Journal of cell biology
影响因子:
--
作者:
Hirano M;Hashimoto S;Yonemura S;Sabe H;Aizawa S
通讯作者:
Aizawa S
影响因子:
4.1
作者:
Warzecha CC;Shen S;Xing Y;Carstens RP
通讯作者:
Carstens RP