Long noncoding RNAs in B-cell development and activation

被引:130
作者
Brazao, Tiago F. [1 ]
Johnson, Jethro S. [2 ]
Muller, Jennifer [1 ]
Heger, Andreas [2 ]
Ponting, Chris P. [2 ]
Tybulewicz, Victor L. J. [1 ,3 ]
机构
[1] Francis Crick Inst, London NW7 1AA, England
[2] Univ Oxford, MRC, Computat Genom Anal & Training Ctr, Funct Genom Unit,Dept Physiol Anat & Genet, Oxford, England
[3] Imperial Coll, London, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
ACUTE LYMPHOBLASTIC-LEUKEMIA; DIVERGENT TRANSCRIPTION; STEM-CELLS; EXPRESSION; DIFFERENTIATION; GENOME; REVEALS; REGULATORS; ELEMENTS; FAS;
D O I
10.1182/blood-2015-11-680843
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Long noncoding RNAs (lncRNAs) are potentially important regulators of cell differentiation and development, but little is known about their roles in Blymphocytes. Using RNAseq and de novo transcript assembly, we identified 4516 lncRNAs expressed in 11 stages of B-cell development and activation. Most of these lncRNAs have not been previously detected, even in the closely related T-cell lineage. Comparison with lncRNAs previously described in human B cells identified 185 mouse lncRNAs that have human orthologs. Using chromatin immunoprecipitation-seq, we classified 20% of the lncRNAs as either enhancer-associated (eRNA) or promoter-associated RNAs. We identified 126 eRNAs whose expression closely correlated with the nearest coding gene, thereby indicating the likely location of numerous enhancers active in the B-cell lineage. Furthermore, using this catalog of newly discovered lncRNAs, we show that PAX5, a transcription factor required to specify the B-cell lineage, bound to and regulated the expression of 109 lncRNAs in pro-B and matureB cells and 184 lncRNAs in acute lymphoblastic leukemia.
引用
收藏
页码:E10 / E19
页数:10
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