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作 者:骆鹏[1] 曹玉婷[1] 莫家兴[1] 翁怀峰 施季森[1] 徐进[1] LUO Peng CAO Yuting MO Jiaxing WENG Huaifeng SHI Jisen XU Jin(Co-Innovotion Center for the Sustainable Forestry in Southern China, College of Forestry, Nanjing Forestry University, Nanjing, 210037, China State-owned Forest Farm of Fujian Yangmeiling, Xiapu 355100, China)
机构地区:[1]南方现代林业协同创新中心南京林业大学林学院,江苏南京210037 [2]福建省霞浦杨梅岭林场,福建霞浦355100
出 处:《南京林业大学学报(自然科学版)》2017年第4期191-196,共6页Journal of Nanjing Forestry University:Natural Sciences Edition
基 金:国家林业公益性行业科研专项项目(201304104);江苏省"六大人才高峰"项目(2014-NY-013);江苏高校优势学科建设工程资助项目(PARD);福建省林木种苗科技攻关五期项目
摘 要:【目的】为了构建柳杉无性系的DNA指纹图谱,准确区分柳杉无性系。【方法】利用SSR标记分析了柳杉89个无性系的遗传多样性和指纹图谱。【结果】11对引物共检测出53个等位点,平均每个SSR位点有5个,变化范围为3~6个;有效等位基因数(Ne)变化范围为1.887 0~4.295 6,平均为3.041 1;Shannon信息指数(I)变化范围为0.774 9~1.556 3,平均为1.208 1。表明SSR标记具有较高的多态性。根据SSR标记特点及引物的顺序,将SSR引物扩增统计的"0"、"1"转换成基因型,通过不同基因型组合,构建了柳杉89个无性系的DNA分子指纹图谱,使每个无性系都获得了1个22位数的指纹图谱号码,同时基于个体间的遗传距离将柳杉89个无性系分为5类。【结论】SSR标记适用于柳杉无性系遗传多样性分析及鉴定,柳杉的遗传多态性处于中等偏高水平。【Objective】Molecular fingerprinting and genetic diversity analysis are important for protecting and managing superior germplasm resources,as well as for identifying superior clones.【Method】In the present study,11 SSR primer pairs were used to assess the genetic diversity and DNA fingerprints of 89 C.fortunei clones.【Result】A total of 53 putative alleles were detected from 11 pairs of primers,with a mean of five putative alleles per locus,ranging from three to six.The number of effective alleles(Ne) ranged from 1.887 0 to 4.295 6,with a mean of 3.041 1,and the Shannon's information index ranged from 0.774 9 to 1.556 3,with a mean of 1.208 1.These findings indicate that SSR markers in C.fortunei exist a relative high polymorphism.Furthermore,according to the characteristics of the SSR markers and primer sequences,the present(recorded as 1) and absent(recorded as 0) collected from amplification by SSR markers were transferred into genetic types.By combining different genetic types code,we established DNA fingerprints of 89 C.fortunei clones,and attached a 22-digit fingerprint number to each clone.The 89 clones were also separated into five clusters based on genetic distance.【Conclusion】SSR markers are suitable for analyzing and identifying the genetic diversity of C.fortune,and C.fortune shows moderate to high genetic diversity.
分 类 号:S791.31[农业科学—林木遗传育种]
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