Vorwerk S, Forneck A
Department of Special Crop Cultivation and Crop Physiology, Section of Viticulture and Biotechnology (370a), University of Hohenheim, D-70593 Stuttgart, Germany.
Genome. 2007 Jul;50(7):660-7. doi: 10.1139/g07-046.
Two AFLP fingerprinting methods were employed to estimate the potential of AFLP fingerprints for the detection of genetic diversity within single founder lineages of grape phylloxera (Daktulosphaira vitifoliae Fitch). Eight clonal lineages, reared under controlled conditions in a greenhouse and reproducing asexually throughout a minimum of 15 generations, were monitored and mutations were scored as polymorphisms between the founder individual and individuals of succeeding generations. Genetic variation was detected within all lineages, from early generations on. Six to 15 polymorphic loci (from a total of 141 loci) were detected within the lineages, making up 4.3% of the total amount of genetic variation. The presence of contaminating extra-genomic sequences (e.g., viral material, bacteria, or ingested chloroplast DNA) was excluded as a source of intraclonal variation. Sequencing of 37 selected polymorphic bands confirmed their origin in mostly noncoding regions of the grape phylloxera genome. AFLP techniques were revealed to be powerful for the identification of reproducible banding patterns within clonal lineages.
采用两种扩增片段长度多态性(AFLP)指纹图谱方法,来评估AFLP指纹图谱在检测葡萄根瘤蚜(Daktulosphaira vitifoliae Fitch)单一创始谱系内遗传多样性方面的潜力。对8个克隆谱系进行了监测,这些谱系在温室的可控条件下饲养,至少经过15代无性繁殖,将创始个体与后代个体之间的突变记为多态性。从早期世代开始,在所有谱系中均检测到了遗传变异。在这些谱系中检测到6至15个多态性位点(总共141个位点),占遗传变异总量的4.3%。作为克隆内变异的一个来源,排除了污染性的基因组外序列(如病毒物质、细菌或摄入的叶绿体DNA)的存在。对37条选定的多态性条带进行测序,证实它们大多起源于葡萄根瘤蚜基因组的非编码区域。结果表明,AFLP技术在识别克隆谱系内可重复的条带模式方面很强大。