A biphasic pattern of gene expression during mouse retina development

被引:37
作者
Zhang, Samuel Shao-Min [1 ]
Xu, Xuming
Liu, Mu-Gen
Zhao, Hongyu
Soares, Marcelo Bento
Barnstable, Colin J.
Fu, Xin-Yuan
机构
[1] Yale Univ, Sch Med, Dept Ophthalmol & Visual Sci, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Dept Epidemiol & Publ Hlth, New Haven, CT 06510 USA
[3] Yale Univ, Sch Med, Dept Genet, New Haven, CT 06510 USA
[4] Northwestern Univ, Childrens Mem Res Ctr, Feinberg Sch Med, Evanston, IL 60208 USA
[5] Indiana Univ, Sch Med, Dept Microbiol & Immunol, Bloomington, IN USA
[6] Penn State Univ, Coll Med, Dept Neural & Behav Sci, Hershey, PA USA
关键词
D O I
10.1186/1471-213X-6-48
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Between embryonic day 12 and postnatal day 21, six major neuronal and one glia cell type are generated from multipotential progenitors in a characteristic sequence during mouse retina development. We investigated expression patterns of retina transcripts during the major embryonic and postnatal developmental stages to provide a systematic view of normal mouse retina development, Results: A tissue-specific cDNA microarray was generated using a set of sequence non-redundant EST clones collected from mouse retina. Eleven stages of mouse retina, from embryonic day 12.5 (E12.5) to postnatal day 21 (PN21), were collected for RNA isolation. Non-amplified RNAs were labeled for microarray experiments and three sets of data were analyzed for significance, hierarchical relationships, and functional clustering. Six individual gene expression clusters were identified based on expression patterns of transcripts through retina development. Two developmental phases were clearly divided with postnatal day 5 (PN5) as a separate cluster. Among 4,180 transcripts that changed significantly during development, approximately 2/3 of the genes were expressed at high levels up until PN5 and then declined whereas the other 1/3 of the genes increased expression from PN5 and remained at the higher levels until at least PN21. Less than 1% of the genes observed showed a peak of expression between the two phases. Among the later increased population, only about 40% genes are correlated with rod photoreceptors, indicating that multiple cell types contributed to gene expression in this phase. Within the same functional classes, however, different gene populations were expressed in distinct developmental phases. A correlation coefficient analysis of gene expression during retina development between previous SAGE studies and this study was also carried out. Conclusion: This study provides a complementary genome-wide view of common gene dynamics and a broad molecular classification of mouse retina development. Different genes in the same functional clusters are expressed in the different developmental stages, suggesting that cells might change gene expression profiles from differentiation to maturation stages. We propose that large-scale changes in gene regulation during development are necessary for the final maturation and function of the retina.
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共 62 条
[1]   THE HUMAN REPLACEMENT HISTONE H3.3B GENE (H3F3B) [J].
ALBIG, W ;
BRAMLAGE, B ;
GRUBER, K ;
KLOBECK, HG ;
KUNZ, J ;
DOENECKE, D .
GENOMICS, 1995, 30 (02) :264-272
[2]  
Altieri Dario C, 2003, Prog Cell Cycle Res, V5, P447
[3]   A MOLECULAR VIEW OF VERTEBRATE RETINAL DEVELOPMENT [J].
BARNSTABLE, CJ .
MOLECULAR NEUROBIOLOGY, 1987, 1 (1-2) :9-46
[4]   MONOCLONAL-ANTIBODIES WHICH RECOGNIZE DIFFERENT CELL-TYPES IN THE RAT RETINA [J].
BARNSTABLE, CJ .
NATURE, 1980, 286 (5770) :231-235
[5]   GABAA receptors in Muller glial cells of the human retina [J].
Biedermann, B ;
Bringmann, A ;
Franze, K ;
Faude, F ;
Wiedemann, P ;
Reichenbach, A .
GLIA, 2004, 46 (03) :302-310
[6]   Genomic analysis of mouse retinal development [J].
Blackshaw, S ;
Harpavat, S ;
Trimarchi, J ;
Cai, L ;
Huang, HY ;
Kuo, WP ;
Weber, G ;
Lee, K ;
Fraioli, RE ;
Cho, SH ;
Yung, R ;
Asch, E ;
Ohno-Machado, L ;
Wong, WH ;
Cepko, CL .
PLOS BIOLOGY, 2004, 2 (09) :1411-1431
[7]   Comprehensive analysis of photoreceptor gene expression and the identification of candidate retinal disease genes [J].
Blackshaw, S ;
Fraioli, RE ;
Furukawa, T ;
Cepko, CL .
CELL, 2001, 107 (05) :579-589
[8]   The roles of intrinsic and extrinsic cues and bHLH genes in the determination of retinal cell fates [J].
Cepko, CL .
CURRENT OPINION IN NEUROBIOLOGY, 1999, 9 (01) :37-46
[9]   The patterning and onset of opsin expression in vertebrate retinae [J].
Cepko, CL .
CURRENT OPINION IN NEUROBIOLOGY, 1996, 6 (04) :542-546
[10]   Identification of novel genes preferentially expressed in the retina using a custom human retina cDNA microarray [J].
Chowers, I ;
Gunatilaka, TL ;
Farkas, RH ;
Qian, J ;
Hackam, AS ;
Duh, E ;
Kageyama, M ;
Wang, CW ;
Vora, A ;
Campochiaro, PA ;
Zack, DJ .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 (09) :3732-3741