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dc.contributor.authorLodish, Harvey F.
dc.contributor.authorChen, Chang-Zheng
dc.contributor.authorBartel, David P.
dc.date.accessioned2004-12-15T23:15:48Z
dc.date.available2004-12-15T23:15:48Z
dc.date.issued2005-01
dc.identifier.urihttp://hdl.handle.net/1721.1/7483
dc.description.abstractMicroRNAs (miRNAs), an abundant class of ~22 nucleotide non-coding RNAs, are thought to play an important regulatory role in animal and plant development at the posttranscriptional level. Many miRNAs cloned from mouse bone marrow cells are differentially regulated in various hematopoietic lineages, suggesting that they might influence hematopoietic lineage differentiation. Some human miRNAs are linked to leukemias: the miR-15a/miR-16 locus is frequently deleted or down-regulated in patients with B-cell chronic lymphocytic leukemia and miR-142 is at a translocation site found in a case of aggressive B-cell leukemia. miR-181, a miRNA upregulated only in the B cell lineage of mouse bone marrow cells, promotes B cell differentiation and inhibits production of CD8⁺ T cells when expressed in hematopoietic stem/progenitor cells. In contrast miR-142s inhibits production of both CD4⁺ and CD8⁺ T cells and does not affect B cells. Collectively, these results indicate that microRNAs are components of the molecular circuitry controlling mouse hematopoiesis and suggest that other microRNAs have similar regulatory roles during other facets of vertebrate development.en
dc.description.sponsorshipSingapore-MIT Alliance (SMA)en
dc.format.extent1625451 bytes
dc.format.mimetypeapplication/pdf
dc.language.isoen
dc.relation.ispartofseriesMolecular Engineering of Biological and Chemical Systems (MEBCS);
dc.subjectmicroRNAen
dc.subjectB cellsen
dc.subjectT cellsen
dc.subjectleukemiaen
dc.subjectlymphomaen
dc.subjectstem cellsen
dc.subjectCD4+en
dc.subjectCD8+en
dc.titleMicroRNAs Modulate Hematopoietic Lineage Differentiationen
dc.typeArticleen


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