Gene cloning of fish interferon / 魚類干擾素基因之選殖

碩士 / 國立海洋大學 / 水產養殖學系 / 84 / In order to study the antivrial machanism induced by poly I:C,
we firsttested and found that the poly I:C dose not cause
cytotoxicity to fishcell lines. We treated 5 different fish cell
lines with poly I:C thentreated with T42G strain IPNV, and found
that RTG-2 cell line preasenthighest antiviral ability in
response to the poly I:C treatment. Whendifferent
concerntractions of poly I:C were applied to the RTG-2 cells,the
antiviral ability of these cells increased as the dosage of poly
I:Cincreased, up to 6 ug/ml of poly I:C. SDS-PAGE
electrophoresis to analysisthe poly I:C treated RTG-2 cell
culture medium showed the present of an extra-protein band of
about 17.4KD by commassie blue staining. In order to confirm
that this protein is induced by poly I:C, we labled the poly I:
Ctreated RTG-2 cells with 35S-methionine,and showed that a
labled protein of about 17.4KD also present in the culture
medium, and the radioactivity ofthis protein band is stronger
than the one in the medium of control not treated with poly I:C.
So we proved that this protein is induced by poly I:Ctreatment.
According to the above data, we think that the interferon gene
is exist inthe RTG-2 cells, so we synthesized squence-specific
primers according to thecDNA squence of flatfish interferon
published by Tamai, to amplify and squenced, which showen 48%
homology when compared with flatfish interferon cDNA. Since
there are stop codens with in the fragment. We need further
studyto evaluate whether this fragment really respresent a part
of fish interferongene.

Identiferoai:union.ndltd.org:TW/084NTOU0086016
Date January 1996
CreatorsWu, chieng-hung, 巫建宏
ContributorsChou Hsin-Yiu, 周信佑
Source SetsNational Digital Library of Theses and Dissertations in Taiwan
Languagezh-TW
Detected LanguageEnglish
Type學位論文 ; thesis
Format54

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