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人类成熟B细胞微小RNA组的鉴定。

Identification of the human mature B cell miRNome.

作者信息

Basso Katia, Sumazin Pavel, Morozov Pavel, Schneider Christof, Maute Roy L, Kitagawa Yukiko, Mandelbaum Jonathan, Haddad Joseph, Chen Chang-Zheng, Califano Andrea, Dalla-Favera Riccardo

机构信息

Institute of Cancer Genetics and Herbert Irving Comprehensive Cancer Center, Columbia University, New York, NY 10032, USA.

出版信息

Immunity. 2009 May;30(5):744-52. doi: 10.1016/j.immuni.2009.03.017. Epub 2009 May 14.

DOI:10.1016/j.immuni.2009.03.017
PMID:19446474
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2764486/
Abstract

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 lymphomagenesis, 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.

摘要

人类基因组中微小RNA(miRNA)的完整集合尚不清楚。由于目前已知的miRNA是通过它们在少数细胞类型中的高丰度表达而被鉴定出来的,许多组织特异性miRNA仍未被发现。为了了解miRNA在B细胞功能和淋巴瘤发生中的作用,我们从处于不同发育阶段(初始、生发中心、记忆)的正常人B细胞以及一个伯基特淋巴瘤细胞系中生成了短RNA文库。克隆和计算分析相结合,鉴定出在正常和/或转化的B细胞文库中表达的178种miRNA(miRNA组)。最值得注意的是,B细胞miRNA组包含75种miRNA,据我们所知,此前尚未有相关报道,其中66种已通过RNA印迹和/或逆转录-聚合酶链反应分析得到验证。许多miRNA在B细胞中以阶段特异性或转化特异性的方式表达,提示其具有特定的功能或病理作用。这些结果为研究miRNA在B细胞发育、免疫功能和淋巴瘤发生中的作用提供了资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e3e/2764486/6f5633b0949f/nihms150218f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e3e/2764486/50bf45fd3740/nihms150218f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e3e/2764486/2f058d63fadb/nihms150218f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e3e/2764486/84437caec857/nihms150218f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e3e/2764486/6f5633b0949f/nihms150218f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e3e/2764486/50bf45fd3740/nihms150218f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e3e/2764486/2f058d63fadb/nihms150218f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e3e/2764486/84437caec857/nihms150218f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e3e/2764486/6f5633b0949f/nihms150218f4.jpg

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