Failure of PCR-RAPD technique to differentiate sex in Mahisefied (Rutilus frisii kutum) from the South Caspian Sea

In order to identify the sex marker in Mahisefied, Rutilus frisii kutum, samples from 5 male and 5 female fish were collected from the south Caspian Sea. Polymerase chain reaction random amplified polymorphic DNA (PCR-RAPD) was performed using 124 primer sets. All bands were numbered using 1 and 0 scores corresponding to the presence or absence of bands, respectively and data were analyzed using RAPDPLOT program. Results indicated that 44 sets of primers did not show any flanking site and produced no bands, while the remaining 80 produced sharp and visible bands on polyacrylamid gel. In total, 1600 bands were scored. However, none of the bands corresponded to either the male or female fish. According to the results it has been concluded that RAPD technique failed to detect sex and cannot be considered as a robust molecular tool for sex differentiation in the studied fish. The reason may be the absence of sex chromosomes in this species or that the genes corresponding to sex differentiation are spread on different autosomal chromosomes with interaction of some environmental factors.

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Bibliographic Details
Main Authors: Pourkazemi, M., Razikazemi, S.
Format: Journal Contribution biblioteca
Language:English
Published: 2011
Subjects:Rutilus frisii kutum, Mahisefid, Random Amplified Polymorphic DNA, Sex determination, Failure, Sex, DNA,
Online Access:http://hdl.handle.net/1834/10411
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spelling dig-aquadocs-1834-104112021-05-19T06:54:10Z Failure of PCR-RAPD technique to differentiate sex in Mahisefied (Rutilus frisii kutum) from the South Caspian Sea Pourkazemi, M. Razikazemi, S. Rutilus frisii kutum Mahisefid Random Amplified Polymorphic DNA Sex determination Failure Sex DNA In order to identify the sex marker in Mahisefied, Rutilus frisii kutum, samples from 5 male and 5 female fish were collected from the south Caspian Sea. Polymerase chain reaction random amplified polymorphic DNA (PCR-RAPD) was performed using 124 primer sets. All bands were numbered using 1 and 0 scores corresponding to the presence or absence of bands, respectively and data were analyzed using RAPDPLOT program. Results indicated that 44 sets of primers did not show any flanking site and produced no bands, while the remaining 80 produced sharp and visible bands on polyacrylamid gel. In total, 1600 bands were scored. However, none of the bands corresponded to either the male or female fish. According to the results it has been concluded that RAPD technique failed to detect sex and cannot be considered as a robust molecular tool for sex differentiation in the studied fish. The reason may be the absence of sex chromosomes in this species or that the genes corresponding to sex differentiation are spread on different autosomal chromosomes with interaction of some environmental factors. Published 2017-11-17T07:25:13Z 2017-11-17T07:25:13Z 2011 Journal Contribution Refereed 1735-3033 http://hdl.handle.net/1834/10411 en pp.235-242 Iran Caspian Sea
institution UNESCO
collection DSpace
country Francia
countrycode FR
component Bibliográfico
access En linea
databasecode dig-aquadocs
tag biblioteca
region Europa del Oeste
libraryname Repositorio AQUADOCS
language English
topic Rutilus frisii kutum
Mahisefid
Random Amplified Polymorphic DNA
Sex determination
Failure
Sex
DNA
Rutilus frisii kutum
Mahisefid
Random Amplified Polymorphic DNA
Sex determination
Failure
Sex
DNA
spellingShingle Rutilus frisii kutum
Mahisefid
Random Amplified Polymorphic DNA
Sex determination
Failure
Sex
DNA
Rutilus frisii kutum
Mahisefid
Random Amplified Polymorphic DNA
Sex determination
Failure
Sex
DNA
Pourkazemi, M.
Razikazemi, S.
Failure of PCR-RAPD technique to differentiate sex in Mahisefied (Rutilus frisii kutum) from the South Caspian Sea
description In order to identify the sex marker in Mahisefied, Rutilus frisii kutum, samples from 5 male and 5 female fish were collected from the south Caspian Sea. Polymerase chain reaction random amplified polymorphic DNA (PCR-RAPD) was performed using 124 primer sets. All bands were numbered using 1 and 0 scores corresponding to the presence or absence of bands, respectively and data were analyzed using RAPDPLOT program. Results indicated that 44 sets of primers did not show any flanking site and produced no bands, while the remaining 80 produced sharp and visible bands on polyacrylamid gel. In total, 1600 bands were scored. However, none of the bands corresponded to either the male or female fish. According to the results it has been concluded that RAPD technique failed to detect sex and cannot be considered as a robust molecular tool for sex differentiation in the studied fish. The reason may be the absence of sex chromosomes in this species or that the genes corresponding to sex differentiation are spread on different autosomal chromosomes with interaction of some environmental factors.
format Journal Contribution
topic_facet Rutilus frisii kutum
Mahisefid
Random Amplified Polymorphic DNA
Sex determination
Failure
Sex
DNA
author Pourkazemi, M.
Razikazemi, S.
author_facet Pourkazemi, M.
Razikazemi, S.
author_sort Pourkazemi, M.
title Failure of PCR-RAPD technique to differentiate sex in Mahisefied (Rutilus frisii kutum) from the South Caspian Sea
title_short Failure of PCR-RAPD technique to differentiate sex in Mahisefied (Rutilus frisii kutum) from the South Caspian Sea
title_full Failure of PCR-RAPD technique to differentiate sex in Mahisefied (Rutilus frisii kutum) from the South Caspian Sea
title_fullStr Failure of PCR-RAPD technique to differentiate sex in Mahisefied (Rutilus frisii kutum) from the South Caspian Sea
title_full_unstemmed Failure of PCR-RAPD technique to differentiate sex in Mahisefied (Rutilus frisii kutum) from the South Caspian Sea
title_sort failure of pcr-rapd technique to differentiate sex in mahisefied (rutilus frisii kutum) from the south caspian sea
publishDate 2011
url http://hdl.handle.net/1834/10411
work_keys_str_mv AT pourkazemim failureofpcrrapdtechniquetodifferentiatesexinmahisefiedrutilusfrisiikutumfromthesouthcaspiansea
AT razikazemis failureofpcrrapdtechniquetodifferentiatesexinmahisefiedrutilusfrisiikutumfromthesouthcaspiansea
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