Effects of RNA degradation on gene expression analysis of human postmortem tissues

被引:89
作者
Lee, J [1 ]
Hever, A [1 ]
Willhite, D [1 ]
Zlotnik, A [1 ]
Hevezi, P [1 ]
机构
[1] Neurocrine Biosci Inc, Dept Mol Med, San Diego, CA 92130 USA
关键词
thymus; RNA quality; GPCR;
D O I
10.1096/fj.04-3552fje
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
The Affymetrix GeneChip platform was used to build a gene expression database of the normal human body. Postmortem human tissues represent a valuable source of biological materials for this type of study, but their use entails some delays before harvesting such tissues. We first evaluated the RNA quality obtained from tissues obtained 3-5 h postmortem and found variations that were both tissue and donor-dependent. RNAs extracted from brain regions were of higher quality than those obtained from the gut, while the cause of death was a significant factor in donor-dependent differences. To avoid these variables, we used rat duodenum to determine the effects of RNA degradation on the analysis of gene expression. Surprisingly, even samples exhibiting significant RNA degradation yielded robust gene expression results, comparable to those obtained using intact samples at a certain signal intensity cutoff. We extended these findings to our human expression database and obtained similar results, indicating that the Affymetrix platform, which is biased to the 3' end of transcripts for detection, can tolerate significant RNA degradation, while still yielding high quality expression data. Our resulting body index expression database is a valuable research tool. As examples of potential uses, we report novel expression sites for four potential therapeutic targets-CCL27, GPR22, GPR113 and GPR128-and as well as a set of thymus-specific genes, including three not previously associated with the thymus.
引用
收藏
页码:1356 / +
页数:25
相关论文
共 41 条
[21]   Thermal effects on reverse transcription: Improvement of accuracy and processivity in cDNA synthesis [J].
Malboeuf, CM ;
Isaacs, SJ ;
Tran, NH ;
Kim, B .
BIOTECHNIQUES, 2001, 30 (05) :1074-+
[22]   The human olfactory receptor gene family [J].
Malnic, B ;
Godfrey, PA ;
Buck, LB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (08) :2584-2589
[23]   Quantitative polymerase chain reaction: Validation of microarray results from postmortem brain studies [J].
Mimmack, ML ;
Brooking, J ;
Bahn, S .
BIOLOGICAL PSYCHIATRY, 2004, 55 (04) :337-345
[24]   Murine CCR9, a chemokine receptor for thymus-expressed chemokine that is up-regulated following pre-TCR signaling [J].
Norment, AM ;
Bogatzki, LY ;
Gantner, BN ;
Bevan, MJ .
JOURNAL OF IMMUNOLOGY, 2000, 164 (02) :639-648
[25]   Cloning and chromosomal mapping of four putative novel human G-protein-coupled receptor genes [J].
ODowd, BF ;
Nguyen, T ;
Jung, BP ;
Marchese, A ;
Cheng, R ;
Heng, HHQ ;
Kolakowski, LF ;
Lynch, KR ;
George, SR .
GENE, 1997, 187 (01) :75-81
[26]  
PAPSIDERO LD, 1981, J NATL CANCER I, V66, P37
[27]   An optimistic view for quantifying mRNA in post-mortem human brain [J].
Preece, P ;
Virley, DJ ;
Costandi, M ;
Coombes, R ;
Moss, SJ ;
Mudge, AW ;
Jazin, E ;
Cairns, NJ .
MOLECULAR BRAIN RESEARCH, 2003, 116 (1-2) :7-16
[28]   Gene expression changes in peripheral blood-derived dendritic cells following exposure to a contact allergen [J].
Ryan, CA ;
Gildea, LA ;
Hulette, BC ;
Dearman, RJ ;
Kimber, I ;
Gerberick, GF .
TOXICOLOGY LETTERS, 2004, 150 (03) :301-316
[29]   Transcriptional profile of postmortem skeletal muscle [J].
Sanoudou, D ;
Kang, PB ;
Haslett, JN ;
Han, M ;
Kunkel, LM ;
Beggs, AH .
PHYSIOLOGICAL GENOMICS, 2004, 16 (02) :222-228
[30]  
Schmidt W. M., 2003, International Journal of Clinical Pharmacology and Therapeutics, V41, P624