Goals of this research project are to collect many mouse cDNA clones and prepare cDNA microarrays containing as many mouse genes as possible. The idea behind this work is to develop a method to monitor the expression levels of a large number of genes in various experimental conditions and to understand global changes of gene expression patterns in development and aging. The systematic analysis of expression patterns of a large number of genes quickly becomes the method of choice for many laboratories to understand biological systems. Accordingly the demand for high quality cDNA libraries and cDNA microarrays is increasing. In addition to 30,000 expressed sequence tags (ESTs) we generated in our previous work, we have generated 30,000 ESTs at NIA during this period. After scoring for redundancy, the 60,000 ESTs have been grouped into 15,275 sets of unique genes. This non-redundant gene set consists of 2132 genes from E7.5 extraembryonic tissue cDNA library, 893 genes from E7.5 embryonic tissue cDNA library, 7692 genes from preimplantation cDNA libraries (unfertilized eggs, fertilized eggs, 2-cell, 4-cell, 8-cell, 16-cell embryos and blastocysts), and 4620 genes. from E12.5 mesonephros and newborn ovary cDNA libraries. Sequence similarity searches against public sequence databases revealed that this gene set includes 3331 (22%) known (named) genes, 3526 (23.1%) new genes with some similarity to named genes, and 8418 (55.1%) new genes. Thus, this set of unique gene contains an unusually high fraction of novel genes. A set of these unique genes was rearrayed and the inserts of individual cDNA clones were amplified by PCR. The PCR products have been spotted onto a nylon membrane to make a cDNA microarray and have been used for differential gene expression analyses of the 15,275 component genes.Future plans include: the improvement of current methods to isolate full-length cDNA clones more efficiently, the expansion of the set of unique genes to 30,000 genes by sequencing more cDNA clones from various embryonic collections, and the preparation of cDNA microarrays from the expanded set of unique genes - Mouse development; cDNA project; EST project; cDNA microarrays

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Intramural Research (Z01)
Project #
1Z01AG000656-01
Application #
6227831
Study Section
Special Emphasis Panel (LG)
Project Start
Project End
Budget Start
Budget End
Support Year
1
Fiscal Year
1999
Total Cost
Indirect Cost
Name
National Institute on Aging
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Sharov, Alexei A (2017) Composite Agency: Semiotics of Modularity and Guiding Interactions. Biosemiotics 10:157-178
Sharov, Alexei A (2016) Coenzyme world model of the origin of life. Biosystems 144:8-17
Sharov, Alexei A (2016) Evolutionary biosemiotics and multilevel construction networks. Biosemiotics 9:399-416
Teratani-Ota, Yusuke; Yamamizu, Kohei; Piao, Yulan et al. (2016) Induction of specific neuron types by overexpression of single transcription factors. In Vitro Cell Dev Biol Anim 52:961-973
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Morgani, Sophie M; Canham, Maurice A; Nichols, Jennifer et al. (2013) Totipotent embryonic stem cells arise in ground-state culture conditions. Cell Rep 3:1945-57
Hammachi, Fella; Morrison, Gillian M; Sharov, Alexei A et al. (2012) Transcriptional activation by Oct4 is sufficient for the maintenance and induction of pluripotency. Cell Rep 1:99-109
Canham, Maurice A; Sharov, Alexei A; Ko, Minoru S H et al. (2010) Functional heterogeneity of embryonic stem cells revealed through translational amplification of an early endodermal transcript. PLoS Biol 8:e1000379
Kunisada, Makoto; Cui, Chang-Yi; Piao, Yulan et al. (2009) Requirement for Shh and Fox family genes at different stages in sweat gland development. Hum Mol Genet 18:1769-78
Sharova, Lioudmila V; Sharov, Alexei A; Nedorezov, Timur et al. (2009) Database for mRNA half-life of 19 977 genes obtained by DNA microarray analysis of pluripotent and differentiating mouse embryonic stem cells. DNA Res 16:45-58

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