Identification of F1 Cassava (<i>Manihot esculenta</i>Crantz) Progeny Using Microsatellite Markers and Capillary Electrophoresis

• 作者: Baguma Yona Ferguson Morag Kaweesi Tadeo Kawuki Robert Kyaligonza Vincent Vuzi Peter
• 来源期刊: 美国植物学期刊(英文)
• 学科: 医学
• 关键词: CASSAVA CROSSES Authenticity of F1 PROGENY Molecular Markers
• 年，卷（期）: 2014,（1）
• 页码范围: 119-125
• 页数: 7页
• 分类号: R73

摘要

Generation of genetic diversity is necessary in improving on the potential of cassava when faced with various biotic and abiotic challenges. Presently, cassava breeders are breeding for a number of traits, such as drought tolerance, early root bulking, yield, starch, beta-carotene, protein, dry matter, pest and disease resistance, by relying on genetic diversity that exists in manihot esculenta germplasm. Controlled pollination is one of the main methods used to generate genetic diversity in cassava. However, the process of controlled pollination especially in an open field is prone to contamination by illegitimate pollen right from the time of pollination, seed collection, nursery bed establishment to planting of the trials. Therefore, authentication of the progeny obtained from cassava crosses is very important for genetic studies. Twelve informative microsatellite markers were used to verify the authenticity of 364 F1 progeny thought to come from four controlled parental crosses. The transmission of each allele at nine microsatellite loci was tracked from parents to progeny in each of the four Namikonga-derived F1 cassava families. Out of the 364 F1 progeny, 317 (87.1%) were true-to-type, 44 (12.1%) were a product of self-pollination and 3 (0.8%) were a product of open pollination. The consistency of the results obtained using microsatellite markers makes this technique a reliable tool for assessing the purity of progeny generated from cassava crosses.