Department of Microbiology, TNO Nutrition and Food Research, P.O. Box 360, NL-3700, AJ Zeist, the Netherlands.
Theor Appl Genet. 1994 Jun;88(3-4):472-8. doi: 10.1007/BF00223663.
In order to study genetic variability at the DNA level in chrysanthemum (Dendranthema grandiflora Tzvelev) PstI and HindIII genomic libraries were constructed. Probes from both libraries were tested for the presence of restriction fragment length polymorphisms (RFLPs). Of the probes from the PstI library 91% appeared to hybridize to low-copy genes, while only 35% of those from the HindIII library appeared to do so. The PstI probes were used in further analyses as 79% of them showed RFLPs, whereas the HindIII low-copy number probes gave only 14% polymorphic patterns. Because of the hexaploid character of chrysanthemum, complex patterns generally consisting of 6-12 fragments were visible on a Southern blot after hybridization. To simplify the genetic analysis, locus-specific polymerase chain reaction (PCR) primers were developed that gave simple polymorphic patterns in a number of cases. The RFLP probes and primers developed will be used in future marker-assisted selection in this polyploid crop.
为了在 DNA 水平上研究菊花(Dendranthema grandiflora Tzvelev)的遗传变异性,构建了 PstI 和 HindIII 基因组文库。测试了来自这两个文库的探针,以检测是否存在限制性片段长度多态性(RFLP)。来自 PstI 文库的探针中有 91%似乎与低拷贝基因杂交,而来自 HindIII 文库的探针中只有 35%似乎如此。由于菊花的六倍体特征,Southern 印迹杂交后通常可见到由 6-12 个片段组成的复杂图谱。为了简化遗传分析,开发了针对特定基因座的聚合酶链反应(PCR)引物,在许多情况下产生了简单的多态性模式。在未来的多倍体作物标记辅助选择中,将使用开发的 RFLP 探针和引物。