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      Mitochondrial D-loop sequence variation among Central Javanese Duck in Indonesia Translated title: Variação de sequências de D-Loop Mitocondrial entre Pato Central Java na Indonésia

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          Abstract

          ABSTRACT. This study was realized to determine the genetic variation of Central Javanese duck based on the D-Loop mtDNA gene. D-loop gene was amplified using PCR technique by specific primer and sequenced using dideoxy termination method with ABI automatic sequencer. ClustalW from MEGA-6.06 software program was employed for multiple alignments of nucleotide sequences. Nucleotide sequences of D-loop gene of mtDMA from the Central Javanese duck were aligned together with other Anas isolates from Genbank using ClustalW of MEGA-6.06 program. The estimation of genetic distance and phylogenetic tree construction were analyzed by Neighbor-Joining method, whereas the calculation of distance matrix was performed using Kimura 2-parameter. Multiple alignments obtained were 720 nucleotides at position 56 to 779 at the 5 'end. The results of the polymorphism analysis on D-loop sequences produced 23 haplotypes. However, this haplotype information does not represent the relationship among the geographical origins of duck with the certain duck species name. Moreover, a total number of 32 variable sites were identified. Insertions were detected in four sequences (126, 155, 771 and 779 nucleotide number). In the phylogenetic analysis, it is safe to conclude that the Central Javanese duck is closely related to Anas platyrhynchos and Anas zonorynchos.

          Translated abstract

          RESUMO. Este estudo foi realizado para determinar a variação genética do pato de Java Central baseado no D-Loop mtDNA. A D-Loop foi amplificada utilizando a técnica de PCR com primer específico e sequenciado usando o método de terminação dideoxi com sequenciador ITB automático. ClustalW do programa software de MEGA-6.06 foi utilizado para alinhamentos de algumas sequências de nucleótidos. Sequências de nucleótidos de D-loop gene da mtDMA do pato de Java Central foram alinhados em conjunto com alguns isolados de Anas que foram obtidos de Genbank utilizando o programa ClustalW do programa MEGA-6.06. A estimativa da distância genética e a estrutura da árvore filogenética foram analisadas com o método Neighbor-Joining, enquanto que o cálculo da matriz de distância foi utilizado o parâmetro-2 Kimura. Os alinhamentos múltiplos obtidos foram 720 nucleótideos na posição 56 a 779 na extremidade 5’. As análises do polimorfismo sequencial do D-loop resultaram em 23 haplótipos. No entanto, esta informação haplótipo não representa a relação entre a origem geográfica de pato com o nome de determinadas espécies do pato. Além disso, num total de 32 sites favoráveis foram identificados. As inserções foram detectadas em quatro sequências (126, 155, 771 e 779 números de nucleotídeos). Na análise filogenética é seguro concluir que o pato de Java Central está estreitamente relacionada com a Anas platyrhynchos e Anas zonorynchos.

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          MEGA6: Molecular Evolutionary Genetics Analysis version 6.0.

          We announce the release of an advanced version of the Molecular Evolutionary Genetics Analysis (MEGA) software, which currently contains facilities for building sequence alignments, inferring phylogenetic histories, and conducting molecular evolutionary analysis. In version 6.0, MEGA now enables the inference of timetrees, as it implements the RelTime method for estimating divergence times for all branching points in a phylogeny. A new Timetree Wizard in MEGA6 facilitates this timetree inference by providing a graphical user interface (GUI) to specify the phylogeny and calibration constraints step-by-step. This version also contains enhanced algorithms to search for the optimal trees under evolutionary criteria and implements a more advanced memory management that can double the size of sequence data sets to which MEGA can be applied. Both GUI and command-line versions of MEGA6 can be downloaded from www.megasoftware.net free of charge.
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            Evidence of three maternal lineages in Near Eastern sheep supporting multiple domestication events.

            The variability of mtDNA was analysed in local sheep breeds reared throughout Turkey, for which a fragment of the D-loop region and the complete cytochrome b were sequenced. Phylogenetic analyses performed independently for the D-loop and the Cyt b gene revealed three clearly separated clusters indicating three major maternal lineages, two of which had been previously described as types B and A. The new type, C, was present in all the breeds analysed and showed considerable mtDNA variability. Divergence time was obtained on the basis of Cyt b gene and was estimated to be around 160,000-170,000 years ago for lineages B and A, whereas the divergence of lineage C proved to have occurred earlier (between 450,000 and 750,000 years ago). These times greatly predate domestication and suggest that the origin of modern sheep breeds was more complex than previously thought and that at least three independent sheep domestication events occurred. Our results, together with archaeological information and the current wild sheep populations in the Near East region support the high importance of this area in the sheep domestication process. Finally, the evidence of a third maternal lineage has important implications regarding the history of modern sheep.
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              Which genetic marker for which conservation genetics issue?

              Conservation genetics focuses on the effects of contemporary genetic structuring on long-term survival of a species. It helps wildlife managers protect biodiversity by identifying a series of conservation units, which include species, evolutionarily significant units (ESUs), management units (MUs), action units (AUs), and family nets (FNs). Although mitochondrial DNA (mtDNA) evolves 5-10 times faster than single-copy nuclear DNA (scnDNA), it records few traces of contemporary events. Thus, mtDNA can be used to resolve taxonomic uncertainties and ESUs. Variable number of tandem repeats (VNTRs) evolve 100-1000 times faster than scnDNA and provide a powerful tool for analyzing recent and contemporary events. VNTR analysis techniques include polymerase chain reaction (PCR)-based microsatellite assays and oligonucleotide probing. Size homoplasy problems in PCR-based microsatellite assays can strongly affect the inference of recent population history. The high homozygosity in endangered species is reflected in a relatively low number and level of variability in microsatellite loci. This combined with "allelic dropout" and "misprinting" errors contributes to the generation of highly biased genetic data following analyses of natural populations. Thus, in conservation genetics, microsatellites are of limited use for identifying ESUs, MUs, and AUs. In contrast to PCR-based microsatellite analysis, oligonucleotide probing avoids errors resulting from PCR amplification. It is particularly suitable for inferring recent population history and contemporary gene flow between fragmented subpopulations. Oligonucleotide fingerprinting generates individual-specific DNA banding patterns and thus provides a highly precise tool for monitoring demography of natural populations. Hence, DNA fingerprinting is powerful for distinguishing ESUs, MUs, AUs, and FNs. The use of oligonucleotide fingerprinting and fecal DNA is opening new areas for conservation genetics.
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                Author and article information

                Contributors
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Journal
                asas
                Acta Scientiarum. Animal Sciences
                Acta Sci., Anim. Sci.
                Editora da Universidade Estadual de Maringá - EDUEM (Maringá, PR, Brazil )
                1806-2636
                1807-8672
                December 2017
                : 39
                : 4
                : 449-456
                Affiliations
                [1] Semarang orgnameUniversitas Negeri Semarang orgdiv1Departamento de Biologia, Faculdade de Matemática e Ciência Natural Indonesia
                [2] Salatiga Jawa Tengah orgnameBalai Besar Penelitian dan Pengembangan Vektor dan Reservoir Penyakit Indonesia
                Article
                S1807-86722017000400449
                10.4025/actascianimsci.v39i4.34352
                560d9821-d976-4ae3-a930-7226a1d4989e

                This work is licensed under a Creative Commons Attribution 4.0 International License.

                History
                : 04 April 2017
                : 24 November 2016
                Page count
                Figures: 0, Tables: 0, Equations: 0, References: 34, Pages: 8
                Product

                SciELO Brazil


                javanês duck,mtDNA,D-loop,Central Javanese duck,genetic variation,variação genética

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