R. Widayanti, Siti Naimah, Rahma Prihutami, Trini Susmiati
{"title":"基于ND1基因核苷酸序列的印尼本地鲶鱼遗传多样性研究","authors":"R. Widayanti, Siti Naimah, Rahma Prihutami, Trini Susmiati","doi":"10.22146/jsv.62755","DOIUrl":null,"url":null,"abstract":"One of the native catfish to Indonesia is the baung fish (Hemibagrus). Baung fish are found in rivers in Sumatra, Kalimantan and Java. The catfish population is declining, thus conservation is needed to prevent extinction. To conduct an effective conservation efforts, molecular studies are needed to confirm the fish species from the three islands. Mitochondrial DNA is one of the markers that is often used to see the lineage and kinship of animals for conservation purposes. The purpose of this study is to determine the genetic diversity of the NADH Dehydrogenase Subunit I (ND1) gene catfish from each of these locations, can be used as a genetic marker. Samples were obtained from their natural habitat, namely Magelang (5), Palembang (3), Riau (2), Samarinda (2), 2 from Sintang, and 3 from Banjarmasin. The DNA of the fish sample was then isolated and then used as a template for amplification of DNA fragments using PCR techniques. Amplikon (PCR product) was then purified by gel extraction and then sequenced to determine the DNA sequence. The potential of DNA sequences as catfish genetic markers was proven by analyzing genetic diversity between species using the MEGA version 7.0 program (Kumar et al., 2016). The sequencing results 972 nucleotides composing the ND gene, and found differences in 268 nucleotide sites and 47 amino acid sites. Based on the nucleotide sequence of the ND1 gene, catfish from the Progo river (Magelang, Central Java), the Musi river (Palembang, Sumatra), the Kampar river (Riau), the Kapuas river (Sintang, Kalimantan), the Martapura river (Banjarmasin), the Mahakam river (Kalimantan) is included in the Hemibagrus sp.; catfish from the Elo river (Magelang, Central Java) belongs to the genus Mystus sp.; catfish from the Bengawan Solo river (Bojonegoro, East Java) belongs to the Pangasius sp.","PeriodicalId":17708,"journal":{"name":"Jurnal Sain Veteriner","volume":"5 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Study of Genetic Diversity of Native Indonesian Catfish Based on Nucleotide Sequences of the ND1 Gene\",\"authors\":\"R. 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The DNA of the fish sample was then isolated and then used as a template for amplification of DNA fragments using PCR techniques. Amplikon (PCR product) was then purified by gel extraction and then sequenced to determine the DNA sequence. The potential of DNA sequences as catfish genetic markers was proven by analyzing genetic diversity between species using the MEGA version 7.0 program (Kumar et al., 2016). The sequencing results 972 nucleotides composing the ND gene, and found differences in 268 nucleotide sites and 47 amino acid sites. 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引用次数: 0
摘要
印度尼西亚的本地鲶鱼之一是baung鱼(半鲶鱼)。Baung鱼在苏门答腊、加里曼丹和爪哇的河流中被发现。鲶鱼的数量正在下降,因此需要保护以防止灭绝。为了进行有效的保护工作,需要进行分子研究来确定三个岛屿的鱼类种类。线粒体DNA是一种标记,通常用于观察动物的血统和亲属关系,以保护动物。本研究的目的是确定鲶鱼NADH脱氢酶亚基I (ND1)基因在这些位点的遗传多样性,是否可以作为遗传标记。样本来自它们的自然栖息地,即马格朗(5只)、巨港(3只)、廖内(2只)、萨玛林达(2只)、辛塘(2只)和班贾玛辛(3只)。然后分离鱼样本的DNA,然后使用PCR技术作为扩增DNA片段的模板。扩增子(PCR产物)经凝胶萃取纯化,测序确定DNA序列。通过使用MEGA version 7.0程序分析物种间的遗传多样性,证明了DNA序列作为鲶鱼遗传标记的潜力(Kumar et al., 2016)。测序结果显示,ND基因由972个核苷酸组成,发现268个核苷酸位点和47个氨基酸位点存在差异。根据ND1基因的核苷酸序列,来自Progo河(Magelang,中爪哇)、Musi河(Palembang,苏门答腊)、Kampar河(廖内省)、Kapuas河(Sintang, Kalimantan)、Martapura河(Banjarmasin)、Mahakam河(Kalimantan)的鲶鱼被包括在Hemibagrus sp.;来自Elo河(中爪哇Magelang)的鲶鱼属于Mystus属;本加万梭罗河(东爪哇Bojonegoro)鲶鱼属鲶鱼科。
Study of Genetic Diversity of Native Indonesian Catfish Based on Nucleotide Sequences of the ND1 Gene
One of the native catfish to Indonesia is the baung fish (Hemibagrus). Baung fish are found in rivers in Sumatra, Kalimantan and Java. The catfish population is declining, thus conservation is needed to prevent extinction. To conduct an effective conservation efforts, molecular studies are needed to confirm the fish species from the three islands. Mitochondrial DNA is one of the markers that is often used to see the lineage and kinship of animals for conservation purposes. The purpose of this study is to determine the genetic diversity of the NADH Dehydrogenase Subunit I (ND1) gene catfish from each of these locations, can be used as a genetic marker. Samples were obtained from their natural habitat, namely Magelang (5), Palembang (3), Riau (2), Samarinda (2), 2 from Sintang, and 3 from Banjarmasin. The DNA of the fish sample was then isolated and then used as a template for amplification of DNA fragments using PCR techniques. Amplikon (PCR product) was then purified by gel extraction and then sequenced to determine the DNA sequence. The potential of DNA sequences as catfish genetic markers was proven by analyzing genetic diversity between species using the MEGA version 7.0 program (Kumar et al., 2016). The sequencing results 972 nucleotides composing the ND gene, and found differences in 268 nucleotide sites and 47 amino acid sites. Based on the nucleotide sequence of the ND1 gene, catfish from the Progo river (Magelang, Central Java), the Musi river (Palembang, Sumatra), the Kampar river (Riau), the Kapuas river (Sintang, Kalimantan), the Martapura river (Banjarmasin), the Mahakam river (Kalimantan) is included in the Hemibagrus sp.; catfish from the Elo river (Magelang, Central Java) belongs to the genus Mystus sp.; catfish from the Bengawan Solo river (Bojonegoro, East Java) belongs to the Pangasius sp.