Gene expression profiling of embryo-derived stem cells reveals candidate genes associated with pluripotency and lineage specificity

被引:171
作者
Tanaka, TS
Kunath, T
Kimber, WL
Jaradat, SA
Stagg, CA
Usuda, M
Yokota, T
Niwa, H
Rossant, J
Ko, MSH [1 ]
机构
[1] NIA, Genet Lab, NIH, Baltimore, MD 21224 USA
[2] Univ Toronto, Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[3] Univ Tokyo, Inst Med Sci, Dept Stem Cell Regulat, Tokyo, Japan
[4] RIKEN, Ctr Dev Biol, Lab Pluripotent Cell Studies, Kobe, Hyogo, Japan
关键词
D O I
10.1101/gr.670002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Large-scale gene expression profiling was performed on embryo-derived stem cell lines to identify molecular signatures of pluripotency and lineage specificity. Analysis of pluripotent embryonic stem (ES) cells, extra embryonic-restricted trophoblast stem (TS) cells, and terminally-differentiated mouse embryo fibroblast (MEF) cells identified expression profiles unique to each cell type, as well as genes common only to ES and TS cells. Whereas most of the MEF-specific genes had been characterized previously, the majority (67%) of the ES-specific genes were novel and did not include known differentiated cell markers. Comparison with microarray data from embryonic material demonstrated that ES-specific genes were underrepresented in all stages sampled, whereas TS-specific genes included known placental markers. Investigation of four novel TS-specific genes showed trophoblast-restricted expression in cell lines and in vivo, whereas one uncharacterized ES-specific gene, Esg-1, was found to be exclusively associated with pluripotency. We suggest that pluripotency requires a set of genes not expressed in other cell types, whereas lineage-restricted stem cells, like TS cells, express genes predictive of their differentiated lineage.
引用
收藏
页码:1921 / 1928
页数:8
相关论文
共 45 条
  • [1] Abe K, 1998, INT J DEV BIOL, V42, P1051
  • [2] Adinolfi S, 1999, BIOPOLYMERS, V51, P153
  • [3] [Anonymous], 1994, MANIPULATING MOUSE E
  • [4] CHANGES IN GENE-EXPRESSION FOLLOWING EXPOSURE OF NULLI-SCCI MURINE EMBRYONAL CARCINOMA-CELLS TO INDUCERS OF DIFFERENTIATION - CHARACTERIZATION OF A DOWN-REGULATED MESSENGER-RNA
    ASTIGIANO, S
    BARKAI, U
    ABARZUA, P
    TAN, S
    HARPER, MI
    SHERMAN, MI
    [J]. DIFFERENTIATION, 1991, 46 (01) : 61 - 67
  • [5] BEDDINGTON RSP, 1989, DEVELOPMENT, V105, P733
  • [6] BIERBAUM P, 1994, CELL GROWTH DIFFER, V5, P37
  • [7] DBEST - DATABASE FOR EXPRESSED SEQUENCE TAGS
    BOGUSKI, MS
    LOWE, TMJ
    TOLSTOSHEV, CM
    [J]. NATURE GENETICS, 1993, 4 (04) : 332 - 333
  • [8] MOLECULAR-CLONING OF A CDNA SEQUENCE ENCODING A TROPHECTODERM-SPECIFIC MARKER DURING MOUSE BLASTOCYST FORMATION
    BRULET, P
    JACOB, F
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (07): : 2328 - 2332
  • [9] The lethal mutation of the mouse wasted (wst) is a deletion that abolishes expression of a tissue-specific isoform of translation elongation factor 1α, encoded by the Eefla2 gene
    Chambers, DM
    Peters, J
    Abbott, CM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (08) : 4463 - 4468
  • [10] Chen GX, 2002, STAT SINICA, V12, P241