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High genetic diversity and small genetic variation among populations of Magnolia wufengensis (Magnoliaceae), revealed by ISSR and SRAP markers

机译:用ISSR和SRAP标记揭示五峰木兰种群的高遗传多样性和小遗传变异

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Background: Genetic diversity and genetic variation of 10 populations and subpopulations of Magnolia wufengensis, a new and endangered endemic species, were examined by inter simple sequence repeat (ISSR) and sequence-related amplified polymorphism (SRAP) molecular markers. Compared with other endangered endemic Magnolia taxa, Magnolia wufengensis holds a relatively high level of genetic variation. Result: Total genetic diversity was found to be 87.7% for ISSR and 88.0% for SRAP markers. For polymorphic loci (P), the effective mean number of alleles (Ae) was 1.414 for ISSR markers and 1.458 for SRAP markers, while the mean expected heterozygosity (H) was 0.256 using ISSR and 0.291 for SRAP markers. Within-population variation was estimated for P as 74.9% using ISSR and 74.6% with SRAP markers; the number of alleles Ae was 1.379 with ISSR and 1.397 for SRAP and H 0.235 with ISSR and 0.247 for SRAP markers. Conclusion: The analysis of molecular variation of both ISSR and SRAP marker systems indicated that most genetic variation is within populations, with values of 90.64% and 82.92% respectively. Mantel tests indicated a moderate association between the two marker systems and a low correlation between genetic and geographic distances. High levels of genetic diversity and low levels of population divergence suggest that genetic drift is not currently of great concern for this species. Severe habitat loss and fragmentation, predominantly ascribed to anthropogenic pressures, caused in-situ developing restriction of this species. Action for conserving this rare species for its long-term survival should be taken immediately.
机译:背景:通过相互简单重复序列(ISSR)和与序列相关的扩增多态性(SRAP)分子标记研究了五种木兰五峰(一种新的濒危特有物种)的遗传多样性和遗传变异。与其他濒危特有木兰类相比,五峰木兰具有较高的遗传变异水平。结果:ISSR和SRAP标记的总遗传多样性分别为87.7%和88.0%。对于多态性位点(P),ISSR标记的等位基因有效平均数(Ae)为1.414,SRAP标记为1.458,而ISSR的平均预期杂合度(H)为0.256,SRAP标记为0.291。使用ISSR估计P的种群内变异为74.9%,使用SRAP标记估计为74.6%;对于ISSR,等位基因Ae的数目为1.379,对于SRAP,等位基因的数目为H,对于ISAP,等位基因的数目为0.235,对于SRAP标记,H等位基因的数目为0.247。结论:对ISSR和SRAP标记系统的分子变异分析表明,大多数遗传变异都在种群内,分别为90.64%和82.92%。壁炉架测试表明,两种标记系统之间存在中等关联,而遗传距离和地理距离之间的相关性较低。高水平的遗传多样性和低水平的种群分化表明,目前对该物种的遗传漂移并不十分关注。主要归因于人为压力的严重栖息地丧失和破碎造成了该物种的原位发育限制。应该立即采取行动保护这种稀有物种的长期生存。

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