Stress-induced changes in gene interactions in human cells

被引:20
|
作者
Nayak, Renuka R. [1 ]
Bernal, William E. [2 ]
Lee, Jessica W. [3 ]
Kearns, Michael J. [4 ,5 ]
Cheung, Vivian G. [5 ,6 ,7 ]
机构
[1] Univ Penn, Perelman Sch Med, Med Scientist Training Program, Philadelphia, PA 19104 USA
[2] Childrens Hosp Philadelphia, Div Rheumatol, Philadelphia, PA 19104 USA
[3] Univ Penn, HHMI Med Res Fellows Program, Philadelphia, PA 19104 USA
[4] Univ Penn, Dept Comp & Informat Sci, Philadelphia, PA 19104 USA
[5] Univ Penn, Dept Pediat, Philadelphia, PA 19104 USA
[6] Univ Penn, Dept Genet, Philadelphia, PA 19104 USA
[7] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
基金
美国国家卫生研究院;
关键词
ENDOPLASMIC-RETICULUM STRESS; IONIZING-RADIATION; DNA-DAMAGE; EXPRESSION; CANCER; DEATH; RESISTANCE; INHIBITION; APOPTOSIS; ATM;
D O I
10.1093/nar/gkt999
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
Cells respond to variable environments by changing gene expression and gene interactions. To study how human cells response to stress, we analyzed the expression of >5000 genes in cultured B cells from nearly 100 normal individuals following endoplasmic reticulum stress and exposure to ionizing radiation. We identified thousands of genes that are induced or repressed. Then, we constructed coexpression networks and inferred interactions among genes. We used coexpression and machine learning analyses to study how genes interact with each other in response to stress. The results showed that for most genes, their interactions with each other are the same at baseline and in response to different stresses; however, a small set of genes acquired new interacting partners to engage in stress-specific responses. These genes with altered interacting partners are associated with diseases in which endoplasmic reticulum stress response or sensitivity to radiation has been implicated. Thus, our findings showed that to understand disease-specific pathways, it is important to identify not only genes that change expression levels but also those that alter interactions with other genes.
引用
收藏
页码:1757 / 1771
页数:15
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