Tissue-specific gene expression analysis of silkworm (Bombyx mori) by quantitative real-time RT-PCR
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The Bombyx mori Microarray Database (BmMDB; http://silkworm. swu.edu.cn/microarray) provides information for tissue-specific gene expression by using the whole-genome oligonucleotide microarray in the silkworm. We analyzed the tissue-specific expression patterns in the silk gland, fat body, and midgut five days of fifth instar larvae during the development of B. mori. To verify the tissue-specific expression, analysis was conducted using quantitative Real-time RT-PCR and the highly expressed endogenous Actin RNA as an intrinsic reference. Finally, we confirmed five genes, (sw15872, sw00692,sw20990, sw05300,and sw2250), out of 18 candidates expressed in two different tissues, which was consistent with the data published by Dr. Xiang’s group, thereby supporting the BmMDB. Further studies for promoter regions of candidate genes can be applied in creating transgenic silkworms as biomedical insects for use in producing biomaterials, and to serve as well-characterized models for understanding the mechanism for the genetic regulation of tissue-specific development.
Abstract
The Bombyx mori Microarray Database (BmMDB; http://silkworm. swu.edu.cn/microarray) provides information for tissue-specific gene expression by using the whole-genome oligonucleotide microarray in the silkworm. We analyzed the tissue-specific expression patterns in the silk gland, fat body, and midgut five days of fifth instar larvae during the development of B. mori. To verify the tissue-specific expression, analysis was conducted using quantitative Real-time RT-PCR and the highly expressed endogenous Actin RNA as an intrinsic reference. Finally, we confirmed five genes, (sw15872, sw00692,sw20990, sw05300,and sw2250), out of 18 candidates expressed in two different tissues, which was consistent with the data published by Dr. Xiang’s group, thereby supporting the BmMDB. Further studies for promoter regions of candidate genes can be applied in creating transgenic silkworms as biomedical insects for use in producing biomaterials, and to serve as well-characterized models for understanding the mechanism for the genetic regulation of tissue-specific development.
참고문헌 (12)
- International Silkworm Genome Consortium, "The genome of a lepidopteran model insect, the silkworm Bombyx mori", Insect Biochem. Mol. Biol., 38, pp.1036~1045 (2008)
- Fuchs, S., "Dynamic processes involved in the pre-vascularization of silk fibroin constructs for bone regeneration using outgrowth endothelial cells", Biomaterials, 30, pp.1329~1338 (2009)
- Gong, Z. H., "Expression of Cholera Toxin B Subunit and Assembly as Functional Oligomers in Silkworm", J. Biochem. Mol. Biol., 38, pp.717~724 (2005)
- Yun, E. Y., "Bombyx mori transferrin: Genomic structure, expression and antimicrobial activity of recombinant protein", Dev. Comp. Immunol., 33, pp.1064~1069 (2009)
- Mita, K., "The genome sequence of silkworm, Bombyx mori", DNA Res., 29, pp.27~35 (2004)
- Mita, K., "The construction of an EST database for Bombyx mori and its application", Proc. Natl. Acad. Sci. U.S.A., 통권 : 100, pp.14121~14126 (2003)
- Ote, M., "Microarray analysis of gene expression profiles in wing discs of Bombyx mori during pupal ecdysis", Insect Biochem. Mol. Biol., 34, pp.775~784 (2004)
- Parthasarathy, R., "Comparative analysis of the development of the mandibular salivary glands and the labial silk glands in the mulberry silkworm, Bombyx mori", Gene. Expr. Patterns., 5, pp.323~339 (2005)
- Xia, Q., "Microarray-based gene expression profiles in multiple tissues of the domesticated silkworm, Bombyx mori", Genome Biol., 8, pp.R162~ (2007)
- Zavallo, D., "Isolation and functional characterization of two novel seed-specific promoters from sunflower (Helianthus annuus L.)", Plant Cell Rep., 29, pp.239~248 (2010)
- Tomita, M., "Transgenic silkworms produce recombinant human type III procollagen in cocoons", Nat. Biotechnol., 21, pp.52~56 (2002)
- Castelló, R., "Quantitative real-time reverse transcription-PCR assay for urokinase plasminogen activator, plasminogen activator inhibitor type 1, and tissue metalloproteinase inhibitor type 1 gene expressions in primary breast cancer", Clin. Chem., 48, pp.1288~1295 (2002)
