Modulation of T-lymphocyte development, growth and cell size by the Myc antagonist and transcriptional repressor Mad1
AUTOR(ES)
Iritani, Brian M.
FONTE
Oxford University Press
RESUMO
Activated lymphocytes must increase in size and duplicate their contents (cell growth) before they can divide. The molecular events that control cell growth in proliferating lymphocytes and other metazoan cells are still unclear. Here, we utilized transgenesis to provide evidence suggesting that the basic helix–loop– helix–zipper (bHLHZ) transcriptional repressor Mad1, considered to be an antagonist of Myc function, inhibits lymphocyte expansion, maturation and growth following pre-T-cell receptor (pre-TCR) and TCR stimulation. Furthermore, we utilized cDNA microarray technology to determine that, of the genes repressed by Mad1, the majority (77%) are involved in cell growth, which correlates with a decrease in size of Mad1 transgenic thymocytes. Over 80% of the genes repressed by Mad1 have previously been found to be induced by Myc. These results suggest that a balance between Myc and Mad levels may normally modulate lymphocyte proliferation and development in part by controlling expression of growth-regulating genes.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=126288Documentos Relacionados
- Inhibition of cell proliferation by the Mad1 transcriptional repressor.
- Function of the c-Myc antagonist Mad1 during a molecular switch from proliferation to differentiation.
- HAT cofactor Trrap regulates the mitotic checkpoint by modulation of Mad1 and Mad2 expression
- Inhibition of T-lymphocyte mitogenic responses and effects on cell functions by bovine herpesvirus 1.
- Modulation of T-lymphocyte differentiation antigens: potential relevance for multiple sclerosis.