Analysis of Nonlinear Gene Expression Progression Reveals Extensive Pathway and Age-Specific Transitions in Aging Human Brains

被引:3
|
作者
Cao, Kajia [1 ,3 ]
Ryvkin, Paul [2 ]
Hwang, Yih-Chii [2 ]
Johnson, F. Brad [1 ,4 ]
Wang, Li-San [1 ,3 ,4 ]
机构
[1] Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA USA
[2] Univ Penn, Genom & Computat Biol Grad Grp, Philadelphia, PA 19104 USA
[3] Univ Penn, Penn Ctr Bioinformat, Philadelphia, PA 19104 USA
[4] Univ Penn, Inst Aging, Philadelphia, PA 19104 USA
来源
PLOS ONE | 2013年 / 8卷 / 10期
关键词
TRANSCRIPTIONAL PROFILES; ALZHEIMERS-DISEASE; OXIDATIVE DAMAGE; AMYLOID-BETA; FATTY-ACIDS; DNA-DAMAGE; BIOLOGY; STRESS; KEGG; RNA;
D O I
10.1371/journal.pone.0074578
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Several recent gene expression studies identified hundreds of genes that are correlated with age in brain and other tissues in human. However, these studies used linear models of age correlation, which are not well equipped to model abrupt changes associated with particular ages. We developed a computational algorithm for age estimation in which the expression of each gene is treated as a dichotomized biomarker for whether the subject is older or younger than a particular age. In addition, for each age-informative gene our algorithm identifies the age threshold with the most drastic change in expression level, which allows us to associate genes with particular age periods. Analysis of human aging brain expression datasets from three frontal cortex regions showed that different pathways undergo transitions at different ages, and the distribution of pathways and age thresholds varies across brain regions. Our study reveals age-correlated expression changes at particular age points and allows one to estimate the age of an individual with better accuracy than previously published methods.
引用
收藏
页数:11
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