Isolation and characterization of MHCIIA gene from Nile tilapi a
El-Semlawy, A., El-Said, K., El-Magd, M., Mohamed, T. (2019). Isolation and characterization of MHCIIA gene from Nile tilapi a. EKB Journal Management System, 40(1), 78-87. doi: 10.21608/djs.2019.139211
Aml A. El-Semlawy; Karim S. El-Said; Mohammed A. El-Magd; Tarek M. Mohamed. "Isolation and characterization of MHCIIA gene from Nile tilapi a". EKB Journal Management System, 40, 1, 2019, 78-87. doi: 10.21608/djs.2019.139211
El-Semlawy, A., El-Said, K., El-Magd, M., Mohamed, T. (2019). 'Isolation and characterization of MHCIIA gene from Nile tilapi a', EKB Journal Management System, 40(1), pp. 78-87. doi: 10.21608/djs.2019.139211
El-Semlawy, A., El-Said, K., El-Magd, M., Mohamed, T. Isolation and characterization of MHCIIA gene from Nile tilapi a. EKB Journal Management System, 2019; 40(1): 78-87. doi: 10.21608/djs.2019.139211

Isolation and characterization of MHCIIA gene from Nile tilapi a

Delta Journal of Science
Article 9, Volume 40, Issue 1, June 2019, Page 78-87  XML PDF (1.54 MB)
Document Type: Research and Reference
DOI: 10.21608/djs.2019.139211
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Authors
Aml A. El-Semlawy1; Karim S. El-Said1; Mohammed A. El-Magd2; Tarek M. Mohamed* 1
1Department of Chemistry (Biochemistry section), Faculty of Science, Tanta University, Egypt
2Department of Anatomy and Embryology, Faculty of Veterinary Medicine, Kafrelsheikh University, Egypt
Abstract
This study was conducted to isolate and characterize the major
histocompatibility complex (MHC) class IIA gene from Nile tilapia
and to compare between different genotypes of this gene following
infection with Aeromonas hydrophila. To achieve our goals PCR was
used to isolate MHC IIA gene following extraction of genomic DNA
from fish blood and then single strand conformational polymorphism
(SSCP) was used to genotype resistant and susceptible/diseased fish.
The results showed 12 nucleotides deletion polymorphisms in MHC
IIA with a product size of 267 bp in control and resistant fish and 255
bp in susceptible/diseased fish(Glover KA, et al.2007) .Additionally ,
sequences out of 50 from susceptible/diseased fish showed a nonsynonymous
G23T SNP which interestingly changed the stop codon
to glycin (G) amino acid with subsequent right shift to the open
reading frame (ORF) . This SNP also resulted in three genotype
(TT ,TG ,GG) with frequencies of 0.9,0.07 and 0.03 respectively .
total protein , albumin and globulin as well as in the phagocytic. The
G23T SNP was also associated with the expression level of MHC IIA
in spleen with lowest expression in susceptible/diseased fish carrying
GG genotype to resistant fish (Xu T et al .,2008). Thus , SNP-disease
resistance association analysis revealed that genotypes (GG and TG)
and alleles (G) of the G23T SNP were high risk for infection
Keywords
Major histocompatibility complex; Genotype; Nile tilapia; SSCPPCR
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