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Asb4, Ata3, and Dcn are novel imprinted genes identified by high-throughput screening using RIKEN cDNA microarray
Yosuke Mizuno1, Yusuke Sotomaru, Yukiko Katsuzawa
1Laboratory for Genome Exploration Research Group, RIKEN Genomic Sciences Center, RIKEN Yokohama Institute, Yokohama 230-0045, Japan.
Biochemical and Biophysical Research Communications
|February 1, 2002
Summary
Researchers identified novel imprinted genes using a high-throughput mouse cDNA microarray. This method efficiently screens for genes with parent-specific expression, aiding in understanding genomic imprinting.
Area of Science:
- Developmental Biology
- Genetics
- Epigenetics
Background:
- Imprinted genes are expressed from only one parental allele (maternal or paternal).
- Identifying imprinted genes is crucial for understanding development and disease.
- Previous methods for identifying imprinted genes were often low-throughput.
Purpose of the Study:
- To develop a high-throughput method for screening novel imprinted genes.
- To identify candidate imprinted genes by comparing gene expression in parthenogenetic and androgenetic embryos.
Main Methods:
- Utilized the RIKEN full-length enriched mouse cDNA microarray.
- Compared gene expression profiles between parthenogenetic and androgenetic embryos.
- Confirmed candidate imprinted genes using normal diploid embryos from reciprocal crosses.
Main Results:
- Identified 25 candidate genes differentially expressed between parthenogenetic and androgenetic embryos.
- Confirmed 8 known imprinted genes and identified 3 novel imprinted genes (Asb4, Ata3, Decorin).
- Some candidates showed no imprinting-associated expression in normal diploid embryos, highlighting the screening method's specificity.
Conclusions:
- The RIKEN cDNA microarray provides a feasible high-throughput method for discovering novel imprinted genes.
- This approach accelerates the identification of genes involved in genomic imprinting.
- The findings contribute to a better understanding of parent-specific gene regulation in mammals.