Gene expression profile of human bone marrow stromal cells: High-throughput expressed sequence tag sequencing analysis

被引:41
|
作者
Jia, L
Young, MF
Powell, J
Yang, LM
Ho, NC
Hotchkiss, R
Robey, PG
Francomano, CA [1 ]
机构
[1] NIA, Genet Lab, NIH, Baltimore, MD 21224 USA
[2] NHGRI, Med Genet Branch, NIH, Bethesda, MD 20892 USA
[3] NIDCR, Craniofacial & Skeletal Dis Branch, NIH, Bethesda, MD 20892 USA
[4] NCI, Ctr Informat Technol, Bioinformat & Mol Anal Sect, Bethesda, MD 20892 USA
[5] Hosp Special Surg, New York, NY 10021 USA
关键词
human bone marrow stromal cells; EST sequencing analysis; novel genes; gene expression profile; data mining;
D O I
10.1006/geno.2001.6683
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Human bone marrow stromal cells (HBMSC) are pluripotent cells with the potential to differentiate into osteoblasts, chondrocytes, myelosupportive stroma, and marrow adipocytes. We used high-throughput DNA sequencing analysis to generate 4258 single-pass sequencing reactions (known as expressed sequence tags, or ESTs) obtained from the 5' (97) and 3' (4161) ends of human cDNA clones from a HBMSC cDNA library. Our goal was to obtain tag sequences from the maximum number of possible genes and to deposit them in the publicly accessible database for ESTs (dbEST of the National Center for Biotechnology Information). Comparisons of our EST sequencing data with nonredundant human mRNA and protein databases showed that the ESTs represent 1860 gene clusters. The EST sequencing data analysis showed 60 novel genes found only in this cDNA library after BLAST analysis against 3.0 million ESTs in NCBI's dbEST database. The BLAST search also showed the identified ESTs that have close homology to known genes, which suggests that these may be newly recognized members of known gene families. The gene expression profile of this cell type is revealed by analyzing both the frequency with which a message is encountered and the functional categorization of expressed sequences. Comparing an EST sequence with the human genomic sequence database enables assignment of an EST to a specific chromosomal region (a process called digital gene localization) and often enables immediate partial determination of intron/exon boundaries within the genomic structure. It is expected that high-throughput EST sequencing and data mining analysis will greatly promote our understanding of gene expression in these cells and of growth and development of the skeleton.
引用
收藏
页码:7 / 17
页数:11
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