Please use this identifier to cite or link to this item: https://doi.org/10.1111/j.1365-2109.2010.02637.x
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dc.titleLysozyme transgenic Atlantic salmon (Salmo salar L.)
dc.contributor.authorFletcher, G.L.
dc.contributor.authorHobbs, R.S.
dc.contributor.authorEvans, R.P.
dc.contributor.authorShears, M.A.
dc.contributor.authorHahn, A.L.
dc.contributor.authorHew, C.L.
dc.date.accessioned2014-10-27T08:32:56Z
dc.date.available2014-10-27T08:32:56Z
dc.date.issued2011-02
dc.identifier.citationFletcher, G.L., Hobbs, R.S., Evans, R.P., Shears, M.A., Hahn, A.L., Hew, C.L. (2011-02). Lysozyme transgenic Atlantic salmon (Salmo salar L.). Aquaculture Research 42 (3) : 427-440. ScholarBank@NUS Repository. https://doi.org/10.1111/j.1365-2109.2010.02637.x
dc.identifier.issn1355557X
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/101045
dc.description.abstractDisease outbreaks are a major constraint to salmon aquaculture worldwide. Therefore, there is considerable interest in finding means to alleviate this problem by enhancing their innate immune system. Because lysozyme is an important component of this system, we generated a line of transgenic Atlantic salmon using a gene construct consisting of a rainbow trout lysozyme gene under the control of the ocean pout antifreeze protein gene promoter op5a (opAFP-rtLys). The results show that the transgene exhibited Mendelian inheritance at both the F1 and the F2 generations and demonstrated that it had integrated into a single chromosome in the genetic founder. Sequence analysis of F2 generation salmon revealed the presence of a complete copy of an intact lysozyme transgene integrant that was identical in sequence to that of the construct. The computationally translated peptide sequence of the lysozyme coding region differed by four amino acids from those present in GenBank (accession nos CAA42084; AAG34564). Reverse transcriptase-polymerase chain reaction analysis demonstrated the expression of the transgene in most body tissues. However, Northern analysis revealed that visible levels of mRNA were only evident in the spleen, skin and kidney. The lysozyme lytic activity of kidney tissue extracts from F2 transgenic salmon was 40% greater than it was in non-transgenic siblings. © 2010 Blackwell Publishing Ltd.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1111/j.1365-2109.2010.02637.x
dc.sourceScopus
dc.subjectAntifreeze protein gene promoter
dc.subjectAquaculture
dc.subjectDisease resistance
dc.subjectOp5a
dc.subjectRainbow trout lysozyme sequence
dc.subjectTransgene expression
dc.typeArticle
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.description.doi10.1111/j.1365-2109.2010.02637.x
dc.description.sourcetitleAquaculture Research
dc.description.volume42
dc.description.issue3
dc.description.page427-440
dc.description.codenAQREF
dc.identifier.isiut000287032900012
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