Generation of expressed sequence tags for immune gene discovery and marker development in the sea squirt, Halocynthia roretzi
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Kim, Young-Ok
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Natl Fisheries Res & Dev Inst, Biotechnol Res Inst, Pusan 619902, South KoreaNatl Fisheries Res & Dev Inst, Biotechnol Res Inst, Pusan 619902, South Korea
Kim, Young-Ok
[1
]
Cho, Hyun Kook
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Pusan Natl Univ, Dept Mol Biol, Pusan 609735, South KoreaNatl Fisheries Res & Dev Inst, Biotechnol Res Inst, Pusan 619902, South Korea
Cho, Hyun Kook
[2
]
Park, Eun-Mi
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Natl Fisheries Res & Dev Inst, Biotechnol Res Inst, Pusan 619902, South KoreaNatl Fisheries Res & Dev Inst, Biotechnol Res Inst, Pusan 619902, South Korea
Park, Eun-Mi
[1
]
Nam, Bo-Hye
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Natl Fisheries Res & Dev Inst, Biotechnol Res Inst, Pusan 619902, South KoreaNatl Fisheries Res & Dev Inst, Biotechnol Res Inst, Pusan 619902, South Korea
Nam, Bo-Hye
[1
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Hur, Young Baek
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Res Ctr Aquaculture Environm, Tongyoung 650943, South KoreaNatl Fisheries Res & Dev Inst, Biotechnol Res Inst, Pusan 619902, South Korea
Hur, Young Baek
[3
]
Lee, Sang-Jun
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Natl Fisheries Res & Dev Inst, Biotechnol Res Inst, Pusan 619902, South KoreaNatl Fisheries Res & Dev Inst, Biotechnol Res Inst, Pusan 619902, South Korea
Lee, Sang-Jun
[1
]
Cheong, JaeHun
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Pusan Natl Univ, Dept Mol Biol, Pusan 609735, South KoreaNatl Fisheries Res & Dev Inst, Biotechnol Res Inst, Pusan 619902, South Korea
Cheong, JaeHun
[2
]
机构:
[1] Natl Fisheries Res & Dev Inst, Biotechnol Res Inst, Pusan 619902, South Korea
[2] Pusan Natl Univ, Dept Mol Biol, Pusan 609735, South Korea
[3] Res Ctr Aquaculture Environm, Tongyoung 650943, South Korea
Expresssed sequence tag (EST) analysis was developed from three cDNA libraries constructed from cells of the digestive tract, gonad, and liver of sea squirt. Randomly selected cDNA clones were partially sequenced to generate a total of 922 ESTs, in which 687 unique ESTs were identified respectively. Results of BLASTX search showed that 612 ESTs (89%) have homology to genes of known function whereas 75 ESTs (11%) were unidentified or novel. Based on the major function of their encoded proteins, the identified clones were classified into ten broad categories. We also identified several kinds of immune-related genes as identifying novel genes. Sequence analysis of ESTs revealed the presence of microsatellite-containing genes that may be valuable for further gene mapping studies. The accumulation of a large number of identified cDNA clones is invaluable for the study of sea squirt genetics and developmental biology. Further studies using cDNA microarrays are needed to identify the differentially expressed transcripts after disease infection.