No specific primer can independently amplify the complete Exon 2 of chicken BLB1 or BLB2 genes

Chicken BLB1 and BLB2 genes are duplicated within MHC-B region that plays a crucial role in disease resistance or susceptibility. To investigate the genetic polymorphism in chicken BLB genes, we analyzed the complete genomic DNA sequences of BLB1 and BLB2 genes from 14 published MHC-B haplotypes (59...

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Autores principales: Li, X.X., Han, L.X., Han, J.L.
Formato: Journal Article
Lenguaje:Inglés
Publicado: 2010
Materias:
Acceso en línea:https://hdl.handle.net/10568/2188
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author Li, X.X.
Han, L.X.
Han, J.L.
author_browse Han, J.L.
Han, L.X.
Li, X.X.
author_facet Li, X.X.
Han, L.X.
Han, J.L.
author_sort Li, X.X.
collection Repository of Agricultural Research Outputs (CGSpace)
description Chicken BLB1 and BLB2 genes are duplicated within MHC-B region that plays a crucial role in disease resistance or susceptibility. To investigate the genetic polymorphism in chicken BLB genes, we analyzed the complete genomic DNA sequences of BLB1 and BLB2 genes from 14 published MHC-B haplotypes (59 kb). Two pairs of primers were chosen or designed to amplify the exon 2 fragments of both genes from six known MHC-B haplotypes. The PCR products were directly sequenced for a preliminary identification of specific variations that were further validated using cloning approach. We found that the specificity of the primers becomes ambiguous to nearly all of the MHC-B haplotypes. Therefore it is impossible to design specific primer according to the complete exon and intron sequences for an independent amplification of complete exon 2 of the BLB1 or BLB2 genes. This calls for an alternative strategy for the investigation of genetic variations in the BLB genes.
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spelling CGSpace21882022-01-29T16:27:46Z No specific primer can independently amplify the complete Exon 2 of chicken BLB1 or BLB2 genes Li, X.X. Han, L.X. Han, J.L. disease resistance chickens Chicken BLB1 and BLB2 genes are duplicated within MHC-B region that plays a crucial role in disease resistance or susceptibility. To investigate the genetic polymorphism in chicken BLB genes, we analyzed the complete genomic DNA sequences of BLB1 and BLB2 genes from 14 published MHC-B haplotypes (59 kb). Two pairs of primers were chosen or designed to amplify the exon 2 fragments of both genes from six known MHC-B haplotypes. The PCR products were directly sequenced for a preliminary identification of specific variations that were further validated using cloning approach. We found that the specificity of the primers becomes ambiguous to nearly all of the MHC-B haplotypes. Therefore it is impossible to design specific primer according to the complete exon and intron sequences for an independent amplification of complete exon 2 of the BLB1 or BLB2 genes. This calls for an alternative strategy for the investigation of genetic variations in the BLB genes. 2010-02-15 2010-08-05T07:49:32Z 2010-08-05T07:49:32Z Journal Article https://hdl.handle.net/10568/2188 en Open Access Li, X.X.; Han, L.X.; Han, J.L. 2010. No specific primer can independently amplify the complete Exon 2 of chicken BLB1 or BLB2 genes. International Journal of Poultry Science 9(2):192-197.
spellingShingle disease resistance
chickens
Li, X.X.
Han, L.X.
Han, J.L.
No specific primer can independently amplify the complete Exon 2 of chicken BLB1 or BLB2 genes
title No specific primer can independently amplify the complete Exon 2 of chicken BLB1 or BLB2 genes
title_full No specific primer can independently amplify the complete Exon 2 of chicken BLB1 or BLB2 genes
title_fullStr No specific primer can independently amplify the complete Exon 2 of chicken BLB1 or BLB2 genes
title_full_unstemmed No specific primer can independently amplify the complete Exon 2 of chicken BLB1 or BLB2 genes
title_short No specific primer can independently amplify the complete Exon 2 of chicken BLB1 or BLB2 genes
title_sort no specific primer can independently amplify the complete exon 2 of chicken blb1 or blb2 genes
topic disease resistance
chickens
url https://hdl.handle.net/10568/2188
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