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首页> 外文期刊>Journal of Applied Phycology >Sex identification and genetic variation of Saccharina (Phaeophyta) gametophytes as revealed by inter-simple sequence repeat (ISSR) markers
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Sex identification and genetic variation of Saccharina (Phaeophyta) gametophytes as revealed by inter-simple sequence repeat (ISSR) markers

机译:简易序列重复(ISSR)标记揭示了糖精(配生植物)配子体的性别鉴定和遗传变异

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Inter-simple sequence repeat (ISSR) polymerase chain reaction (PCR) markers were utilized to investigate the genetic variation between male and female gametophyte populations of strains Rongfu and 901 of Saccharina. In total, 11 ISSR primers were able to generate 135 satisfactory and reproducible loci, of which 134 were polymorphic with 99.26 % polymorphism. The percentages of polymorphism of female gametophyte populations (60 and 62 % for their respective strains) were higher than those of the males (53 %), and the Nei's genetic diversity and Shannon's information index showed a similar tendency. The clustering of gametophytes of the same sex from each strain was well resolved by both an unweighted paired group method using the arithmetic average and a principal component analysis, suggesting that any male/female gametophyte pair could represent each strain. However, a single pair was not adequate for germplasm maintenance because the genetic variance among individuals within a population accounted for 57.45 % of the total (P < 0.0001), as shown by the analysis of molecular variance. The gametophyte sex could be identified by amplification with primer UBC809 because of a differential band present in the females. According to the sequence of this band, a pair of ISSR-derived sequence-characterized amplified region (SCAR) primers was designed. With the primers, one female-specific fragment was detected using PCR and Southern blot hybridization. This converted SCAR marker was localized on one unique chromosome of the female gametophytes of these two strains by use of fluorescence in situ hybridization, confirming that it was a female chromosome-specific marker.
机译:利用简单序列间重复(ISSR)聚合酶链反应(PCR)标记研究了荣糖和901糖酵母菌株的雄配子体和雌配子体群体之间的遗传变异。总共有11个ISSR引物能够产生135个满意且可重复的基因座,其中134个为多态性,具有99.26%的多态性。女性配子体种群的多态性百分比(分别为60%和62%)高于男性(53%),Nei的遗传多样性和Shannon信息指数也显示出相似的趋势。通过使用算术平均值的非加权配对方法和主成分分析,可以很好地解决每个菌株中同性配子体的聚类,这表明任何雄/母配子体对都可以代表每个菌株。但是,单对不足以维持种质,因为分子变异分析表明,种群中个体之间的遗传变异占总数的57.45%(P <0.0001)。由于母体中存在差异带,可以通过用引物UBC809扩增来鉴定配子体性别。根据该条带的序列,设计了一对ISSR衍生的序列特征扩增区(SCAR)引物。使用引物,使用PCR和Southern blot杂交检测到一个女性特异性片段。通过使用荧光原位杂交,将该转化的SCAR标记物定位在这两个菌株的雌配子体的一个独特染色体上,证实它是女性染色体特异性标记物。

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