Pensel S M, Vilardi J C, Remis M I
Departamento de Ecología, Genética y Evolución, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Argentina.
Genome. 2005 Dec;48(6):971-6. doi: 10.1139/g05-076.
RFLP analysis of mtDNA in natural populations is a valuable tool for phylogeographic and population genetic studies. The amplification of long DNA fragments using universal primers may contribute to the development of novel homologous probes in species for which no previous genomic information is available. Here we report how we obtained the complete mtDNA genome of Sinipta dalmani (Orthoptera) in 2 fragments (7 and 9 kb) using primers of conserved regions. The specificity of the PCR reactions was ultimately confirmed by several lines of evidence. These fragments were used as a probe for a mtDNA RFLP study in S. dalmani that analyzed the pattern of haplotype distribution and nucleotide diversity within and among chromosomally differentiated natural populations. Our results suggest that the restriction in gene flow detected at the molecular level may explain the chromosome differentiation detected previously and the maintenance of chromosome polymorphism in some areas of S. dalmani geographic distribution.
对自然种群中线粒体DNA(mtDNA)进行限制性片段长度多态性(RFLP)分析,是系统地理学和种群遗传学研究的一项重要工具。使用通用引物扩增长DNA片段,可能有助于为尚无基因组信息的物种开发新型同源探针。在此,我们报告了如何利用保守区域的引物,在两个片段(7 kb和9 kb)中获得了东方蝼蛄(直翅目)的完整线粒体基因组。PCR反应的特异性最终通过多条证据得以证实。这些片段被用作东方蝼蛄线粒体DNA RFLP研究的探针,该研究分析了染色体分化的自然种群内部和种群间的单倍型分布模式及核苷酸多样性。我们的结果表明,在分子水平检测到的基因流限制,可能解释了先前检测到的染色体分化以及东方蝼蛄地理分布某些区域中染色体多态性的维持。