Putative "stemness" gene jam-B is not required for maintenance of stem cell state in embryonic, neural, or hematopoietic stem cells

Mol Cell Biol. 2006 Sep;26(17):6557-70. doi: 10.1128/MCB.00729-06.

Abstract

Many genes have been identified that are specifically expressed in multiple types of stem cells in their undifferentiated state. It is generally assumed that at least some of these putative "stemness" genes are involved in maintaining properties that are common to all stem cells. We compared gene expression profiles between undifferentiated and differentiated embryonic stem cells (ESCs) using DNA microarrays. We identified several genes with much greater signal in undifferentiated ESCs than in their differentiated derivatives, among them the putative stemness gene encoding junctional adhesion molecule B (Jam-B gene). However, in spite of the specific expression in undifferentiated ESCs, Jam-B mutant ESCs had normal morphology and pluripotency. Furthermore, Jam-B homozygous mutant mice are fertile and have no overt developmental defects. Moreover, we found that neural and hematopoietic stem cells recovered from Jam-B mutant mice are not impaired in their ability to self-renew and differentiate. These results demonstrate that Jam-B is dispensable for normal mouse development and stem cell identity in embryonic, neural, and hematopoietic stem cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Adhesion Molecules / deficiency
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / metabolism*
  • Cell Differentiation
  • Cells, Cultured
  • Crosses, Genetic
  • Embryo, Mammalian / cytology*
  • Female
  • Gene Expression Regulation
  • Gene Targeting
  • Hematopoietic Stem Cells / cytology*
  • Heterozygote
  • Immunoglobulins / deficiency
  • Immunoglobulins / genetics
  • Immunoglobulins / metabolism*
  • Male
  • Membrane Proteins / deficiency
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mice
  • Mice, Knockout
  • Microarray Analysis
  • Multipotent Stem Cells / cytology
  • Mutation / genetics
  • Nerve Tissue / cytology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Testis / cytology

Substances

  • Cell Adhesion Molecules
  • Immunoglobulins
  • Jam2 protein, mouse
  • Membrane Proteins
  • RNA, Messenger