Upregulation of the let-7 microRNA with precocious development in lin-12/Notch hypermorphic Caenorhabditis elegans mutants

被引:24
作者
Solomon, Aharon [1 ]
Mian, Yousaf [1 ]
Ortega-Cava, Cesar [1 ]
Liu, Victor Won Tat [1 ,3 ]
Gurumurthy, Channabasavaiah Basavaraju [2 ]
Naramura, Mayumi [1 ]
Band, Vimla [2 ,3 ]
Band, Hamid [1 ,2 ,3 ]
机构
[1] Evanston NW Healthcare Res Inst, Div Mol Oncol, Evanston, IL USA
[2] Evanston NW Healthcare Res Inst, Div Canc Biol, Evanston, IL USA
[3] Northwestern Univ, Dept Biochem Mol Biol & Cell Biol, Weinberg Coll Arts & Sci, Evanston, IL 60201 USA
关键词
heterochronic genes; developmental timing; lin-12/Notch; let-7; lin-41; microRNA molting; cell fate; seam cells;
D O I
10.1016/j.ydbio.2007.12.046
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The lin-12/Notch signaling pathway is conserved from worms to humans and is a master regulator of metazoan development. Here, we demonstrate that lin-12/Notch gain-of-function (gf) animals display precocious alae at the L4 larval stage with a significant increase in let-7 expression levels. Furthermore, lin-12(gf) animals display a precocious and higher level of let-7 gfp transgene expression in seam cells at L3 stage. Interestingly, lin-12(gf) mutant rescued the lethal phenotype of let-7 mutants similar to other known heterochronic mutants. We propose that lin-12/Notch signaling pathway functions in late developmental timing, upstream of or in parallel to the let-7 heterochronic pathway. Importantly, the human microRNA let-7a was also upregulated in various human cell lines in response to Notch1 activation, suggesting an evolutionarily conserved cross-talk between let-7 and the canonical lin-12/Notch signaling pathway. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:191 / 199
页数:9
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