m6A-Dependent RNA Dynamics in T Cell Differentiation

被引:31
|
作者
Furlan, Mattia [1 ,2 ,3 ]
Galeota, Eugenia [1 ]
de Pretis, Stefano [1 ]
Caselle, Michele [2 ,3 ]
Pelizzola, Mattia [1 ]
机构
[1] Fdn Ist Italiano Tecnol, Ctr Genom Sci, I-20139 Milan, Italy
[2] Univ Turin, Phys Dept, I-10125 Turin, Italy
[3] Univ Turin, INFN, I-10125 Turin, Italy
来源
GENES | 2019年 / 10卷 / 01期
关键词
RNA-seq; RNA dynamics; m6A; RNA modifications; RNA metabolic labeling; mathematical modeling; PRE-MESSENGER-RNA; M(6)A; METHYLATION; STEM; TRANSLATION; DEMETHYLASE; IMPACTS; REVEALS; M6A;
D O I
10.3390/genes10010028
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
N6-methyladenosine (m6A) is the most abundant RNA modification. It has been involved in the regulation of RNA metabolism, including degradation and translation, in both physiological and disease conditions. A recent study showed that m6A-mediated degradation of key transcripts also plays a role in the control of T cells homeostasis and IL-7 induced differentiation. We re-analyzed the omics data from that study and, through the integrative analysis of total and nascent RNA-seq data, we were able to comprehensively quantify T cells RNA dynamics and how these are affected by m6A depletion. In addition to the expected impact on RNA degradation, we revealed a broader effect of m6A on RNA dynamics, which included the alteration of RNA synthesis and processing. Altogether, the combined action of m6A on all major steps of the RNA life-cycle closely re-capitulated the observed changes in the abundance of premature and mature RNA species. Ultimately, our re-analysis extended the findings of the initial study, focused on RNA stability, and proposed a yet unappreciated role for m6A in RNA synthesis and processing dynamics.
引用
收藏
页数:9
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