Uncovering regulatory pathways that effect hematopoietic stem cell function using 'genetical genomics'

Leonid Bystrykh, Ellen Weersing, Bert Dontje, Sue Sutton, Mathew T. Pletcher, Tim Wiltshire, Andrew I. Su, Edo Vellenga, Jintao Wang, Kenneth F. Manly, Lu Lu, Elissa J. Chesler, Rudi Alberts, Ritsert C. Jansen, Robert W. Williams, M. Cooke, MT Pletcher, G de Haan*, AI Su, JT WangKF Manly, EJ Chesler, O. Williams

*Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    330 Citations (Scopus)
    238 Downloads (Pure)

    Abstract

    We combined large-scale mRNA expression analysis and gene mapping to identify genes and loci that control hematopoietic stem cell (HSC) function. We measured mRNA expression levels in purified HSCs isolated from a panel of densely genotyped recombinant inbred mouse strains. We mapped quantitative trait loci (QTLs) associated with variation in expression of thousands of transcripts. By comparing the physical transcript position with the location of the controlling QTL, we identified polymorphic cis-acting stem cell genes. We also identified multiple trans-acting control loci that modify expression of large numbers of genes. These groups of coregulated transcripts identify pathways that specify variation in stem cells. We illustrate this concept with the identification of candidate genes involved with HSC turnover. We compared expression QTLs in HSCs and brain from the same mice and identified both shared and tissue-specific QTLs. Our data are accessible through WebQTL, a web-based interface that allows custom genetic linkage analysis and identification of coregulated transcripts.
    Original languageEnglish
    Pages (from-to)225 - 232
    Number of pages8
    JournalNature Genetics
    Volume37
    Issue number3
    DOIs
    Publication statusPublished - Mar-2005

    Keywords

    • MOUSE
    • MICE
    • IDENTIFICATION
    • DISSECTION
    • LESSONS

    Fingerprint

    Dive into the research topics of 'Uncovering regulatory pathways that effect hematopoietic stem cell function using 'genetical genomics''. Together they form a unique fingerprint.

    Cite this