scholarly journals Microarray analysis reveals a major direct role of DNA copy number alteration in the transcriptional program of human breast tumors

2002 ◽  
Vol 99 (20) ◽  
pp. 12963-12968 ◽  
Author(s):  
J. R. Pollack ◽  
T. Sorlie ◽  
C. M. Perou ◽  
C. A. Rees ◽  
S. S. Jeffrey ◽  
...  
2016 ◽  
Vol 17 (6) ◽  
pp. 814 ◽  
Author(s):  
Chen-Sung Lin ◽  
Hui-Ting Lee ◽  
Ming-Huei Lee ◽  
Siao-Cian Pan ◽  
Chen-Yeh Ke ◽  
...  

2009 ◽  
Vol 6 (4) ◽  
pp. 245-249
Author(s):  
Mengquan Li ◽  
Jingruo Li ◽  
Mingxun Chen ◽  
Juntao Bao

2010 ◽  
Vol 83 (1) ◽  
pp. 52-62 ◽  
Author(s):  
Timothy Wai ◽  
Asangla Ao ◽  
Xiaoyun Zhang ◽  
Daniel Cyr ◽  
Daniel Dufort ◽  
...  

2001 ◽  
Vol 98 (14) ◽  
pp. 7952-7957 ◽  
Author(s):  
A. N. Jain ◽  
K. Chin ◽  
A.-L. Borresen-Dale ◽  
B. K. Erikstein ◽  
P. E. Lonning ◽  
...  

2020 ◽  
Author(s):  
John D. Laver ◽  
Jimmy Ly ◽  
Allison K. Winn ◽  
Angelo Karaiskakis ◽  
Sichun Lin ◽  
...  

SUMMARYG3BP RNA-binding proteins are important components of stress granules (SGs). Here we analyze the role of Drosophila G3BP, Rasputin (RIN), in unstressed cells, where RIN is not SG associated. Immunoprecipitation followed by microarray analysis identified over 550 mRNAs that copurify with RIN. The mRNAs found in SGs are long and translationally silent. In contrast, we find that RIN-bound mRNAs, which encode core components of the transcription, splicing and translation machinery, are short, stable and highly translated. We show that RIN is associated with polysomes and provide evidence for a direct role for RIN and its human homologs in stabilizing and upregulating the translation of their target mRNAs. We propose that when cells are stressed the resulting incorporation of RIN/G3BPs into SGs sequesters them away from their short target mRNAs. This would downregulate the expression of these transcripts, even though they are not incorporated into stress granules.


2021 ◽  
Vol 6 (1) ◽  
pp. 53-73
Author(s):  
Junfeng Liu ◽  
Harner Harner ◽  
Harry Yang

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