Identification of the Human Mature B Cell miRNome

被引:134
作者
Basso, Katia [1 ,2 ,8 ]
Sumazin, Pavel [3 ]
Morozov, Pavel [3 ]
Schneider, Christof [1 ,2 ,9 ]
Maute, Roy L. [1 ,2 ]
Kitagawa, Yukiko [1 ,2 ]
Mandelbaum, Jonathan [1 ,2 ]
Haddad, Joseph, Jr. [4 ]
Chen, Chang-Zheng [10 ]
Califano, Andrea [1 ,2 ,3 ,5 ]
Dalla-Favera, Riccardo [1 ,2 ,6 ,7 ]
机构
[1] Columbia Univ, Inst Canc Genet, New York, NY 10032 USA
[2] Columbia Univ, Herbert Irving Comprehens Canc Ctr, New York, NY 10032 USA
[3] Columbia Univ, Joint Ctr Syst Biol, New York, NY 10032 USA
[4] Columbia Univ, Dept Otolaryngol, New York, NY 10032 USA
[5] Columbia Univ, Dept Biomed Informat, New York, NY 10032 USA
[6] Columbia Univ, Dept Pathol, New York, NY 10032 USA
[7] Columbia Univ, Dept Genet & Dev, New York, NY 10032 USA
[8] Univ Padua, Dept Pediat, I-35100 Padua, Italy
[9] Univ Ulm, Dept Internal Med 3, D-89081 Ulm, Germany
[10] Stanford Univ, Sch Med, Dept Microbiol & Immunol, Stanford, CA 94305 USA
关键词
POSTTRANSCRIPTIONAL REGULATION; EXPRESSION; MICRORNAS; BIOGENESIS; MECHANISMS; MIRBASE; TARGETS;
D O I
10.1016/j.immuni.2009.03.017
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The full set of microRNAs (miRNAs) in the human genome is not known. Because presently known miRNAs have been identified by virtue of their abundant expression in a few cell types, many tissue-specific miRNAs remain unrevealed. To understand the role of miRNAs in B cell function and lymphoma-genesis, we generated short-RNA libraries from normal human B cells at different stages of development (naive, germinal center, memory) and from a Burkitt lymphoma cell line. A combination of cloning and computational analysis identified 178 miRNAs (miRNome) expressed in normal and/or transformed B cell libraries. Most notably, the B cell miRNome included 75 miRNAs which to our knowledge have not been previously reported and of which 66 have been validated by RNA blot and/or RT-PCR analyses. Numerous miRNAs were expressed in a stage- or transformation-specific fashion in B cells, suggesting specific functional or pathologic roles. These results provide a resource for studying the role of miRNAs in B cell development, immune function, and lymphomagenesis.
引用
收藏
页码:744 / 752
页数:9
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