CAJ | 학술논문

采用ISSR分子标记技术,对吉富尼罗罗非鱼群体（GF）、尼罗罗非鱼群体Ⅰ（NLⅠ）、尼罗罗非鱼群体Ⅱ（NLⅡ）、尼罗罗非鱼群体Ⅲ（NLⅢ）和尼罗罗非鱼群体Ⅳ（NLⅣ）的遗传多样性进行分析。用81个ISSR引物对5个尼罗罗非鱼群体进行扩增,15个ISSR引物获得多态片段。根据Nei＇s遗传距离矩阵构建了5个尼罗罗非鱼群体的遗传关系树状图。UPGMA聚类图表明：NLⅢ群体和NLⅣ群体最先聚在一起;其次二者再与GF群体聚在一起;NLⅠ群体与NLⅡ群体聚在一起。分析结果显示：GF群体与其它4个罗非鱼群体区分较明显;用UBC835扩增的500 bp片段为GF所特有,可作为区别GF和其它尼罗罗非鱼的分子标记。
채용ISSR분자표기기술,대길부니라라비어군체（GF）、니라라비어군체Ⅰ（NLⅠ）、니라라비어군체Ⅱ（NLⅡ）、니라라비어군체Ⅲ（NLⅢ）화니라라비어군체Ⅳ（NLⅣ）적유전다양성진행분석。용81개ISSR인물대5개니라라비어군체진행확증,15개ISSR인물획득다태편단。근거Nei＇s유전거리구진구건료5개니라라비어군체적유전관계수상도。UPGMA취류도표명：NLⅢ군체화NLⅣ군체최선취재일기;기차이자재여GF군체취재일기;NLⅠ군체여NLⅡ군체취재일기。분석결과현시：GF군체여기타4개라비어군체구분교명현;용UBC835확증적500 bp편단위GF소특유,가작위구별GF화기타니라라비어적분자표기。
ISSR analysis was used to investigate the genetic relationships of five Nile Tilapia populations from different areas called GF,NLⅠ,NLⅡ,NLⅢ and NLⅣ in this paper.Among 81 ISSR primers,15 primers were able to generate highly reproducibly polymorphic DNA fragments.The genetic trees were constructed based on ISSR amplification finger printings using unweighted pair group method for arithmetic averages analysis(UPGMA).According to the tree,Population NL Ⅲ and NL Ⅳ formed one branch first,then grouped with population GF.Population NLⅠand NLⅡ formed another branch.This result showed that population GF separated from other Nile Tilapias populations;The 500 bp band amplified by primer UBC835 could distinguish population GF from other Nile Tilapia populations.