In situ-synthesized novel microarray optimized for mouse stem cell and early developmental expression profiling

被引:86
作者
Carter, MG
Hamatani, T
Sharov, AA
Carmack, CE
Qian, Y
Aiba, K
Ko, NT
Dudekula, DB
Brzoska, PM
Hwang, SS
Ko, MSH [1 ]
机构
[1] NIA, Genet Lab, Dev Genom & Aging Sect, NIH, Bethesda, MD 20892 USA
[2] Agilent Technol, Palo Alto, CA 94304 USA
关键词
D O I
10.1101/gr.878903
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
Applications of microarray technologies to mouse embryology/genetics have been limited, due to the nonavailability of microarrays containing large numbers of embryonic genes and the gap between microgram quantities of RNA required by typical microarray methods and the miniscule amounts of tissue available to researchers. To overcome these problems, we have developed a microarray platform containing in situ-synthesized 60-mer oligonucleotide probes representing approximately 22,000 unique mouse transcripts, assembled primarily from sequences of stem cell and embryo cDNA libraries. We have optimized RNA labeling protocols and experimental designs to use as little as 2 ng total RNA reliably and reproducibly. At least 98% of the probes contained in the microarray correspond to clones in our publicly available collections, making cDNAs readily available for further experimentation on genes of interest. These characteristics, combined with the ability to profile very small samples, make this system a resource for stem cell and embryogenomics research.
引用
收藏
页码:1011 / 1021
页数:11
相关论文
共 43 条
[1]   A Bayesian framework for the analysis of microarray expression data: regularized t-test and statistical inferences of gene changes [J].
Baldi, P ;
Long, AD .
BIOINFORMATICS, 2001, 17 (06) :509-519
[2]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[3]   Resolution of pluripotential intermediates in murine hematopoietic differentiation by global complementary DNA amplification from single cells: confirmation of assignments by expression profiling of cytokine receptor transcripts [J].
Billia, F ;
Barbara, M ;
McEwen, J ;
Trevisan, M ;
Iscove, NN .
BLOOD, 2001, 97 (08) :2257-2268
[4]   Assessment of the parallelization approach of d2_cluster for high-performance sequence clustering [J].
Carpenter, JE ;
Christoffels, A ;
Weinbach, Y ;
Hide, WA .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 2002, 23 (07) :755-757
[5]  
Chun JY, 1999, DEV DYNAM, V216, P257, DOI 10.1002/(SICI)1097-0177(199911)216:3<257::AID-DVDY4>3.0.CO
[6]  
2-0
[7]   IMPLANTATION AND THE PLACENTA - KEY PIECES OF THE DEVELOPMENT PUZZLE [J].
CROSS, JC ;
WERB, Z ;
FISHER, SJ .
SCIENCE, 1994, 266 (5190) :1508-1518
[8]   A new member of the mouse prolactin (PRL)-like protein-C subfamily, PRL-like protein-Cα:: Structure and expression [J].
Dai, GL ;
Chapman, BM ;
Liu, B ;
Orwig, KE ;
Wang, DH ;
White, RA ;
Preuett, B ;
Soares, MJ .
ENDOCRINOLOGY, 1998, 139 (12) :5157-5163
[9]   Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868
[10]  
Hamilton R T, 1990, Curr Top Dev Biol, V24, P193, DOI 10.1016/S0070-2153(08)60088-5