Authors :
Ojoawo H.T; Ogunpaimo O. J; Ilori B. M, Wheto, M; Adeleke, M. A.; Adebambo, A. O.; Adebambo, O. A.
Volume/Issue :
Volume 5 - 2020, Issue 4 - April
Google Scholar :
http://bitly.ws/9nMw
Scribd :
https://bit.ly/2W4VqVi
Abstract :
Insulin like Growth Factor 1 gene is a
biological and positional candidate gene known to play
an important role in growth, proliferation and
differentiation, body composition, metabolism, skeletal
characteristics, growth of adipose tissue and fat
deposition in chicken. The polymorphisms of Insulin
like Growth Factor 1 gene were investigated in the
FUNAAB Alpha and Marshall Broiler chicken
populations. A total of 642 FUNAAB Alpha dual
purpose, 67 Marshall and 118 FUNAAB Alpha Broiler
chickens were used. Blood samples were collected
through the wing vein of each chicken with the use of a
5ml disposable syringe. Genomic Deoxyribonucleic acid
was extracted from the blood samples using
ZymobeadTM Deoxyribonucleic acid extraction kit
which was amplified using Polymerase Chain Reaction.
The Polymerase Chain Reaction products were
electrophoresed and amplicons obtained were digested
with HinfI which was then electrophoresed on 1.5%
agarose gel. Results obtained indicated that there was
no observed polymorphism in the exons of the Insulin
like Growth Factor 1 gene. However, the restriction
analysis revealed two alleles; A and C in the promoter
region.
Keywords :
FUNAAB Alpha.
Insulin like Growth Factor 1 gene is a
biological and positional candidate gene known to play
an important role in growth, proliferation and
differentiation, body composition, metabolism, skeletal
characteristics, growth of adipose tissue and fat
deposition in chicken. The polymorphisms of Insulin
like Growth Factor 1 gene were investigated in the
FUNAAB Alpha and Marshall Broiler chicken
populations. A total of 642 FUNAAB Alpha dual
purpose, 67 Marshall and 118 FUNAAB Alpha Broiler
chickens were used. Blood samples were collected
through the wing vein of each chicken with the use of a
5ml disposable syringe. Genomic Deoxyribonucleic acid
was extracted from the blood samples using
ZymobeadTM Deoxyribonucleic acid extraction kit
which was amplified using Polymerase Chain Reaction.
The Polymerase Chain Reaction products were
electrophoresed and amplicons obtained were digested
with HinfI which was then electrophoresed on 1.5%
agarose gel. Results obtained indicated that there was
no observed polymorphism in the exons of the Insulin
like Growth Factor 1 gene. However, the restriction
analysis revealed two alleles; A and C in the promoter
region.