详细信息
Chromosome microdissection, cloning and painting of the chromosome 1 in poplar (Populus tremula) ( EI收录)
文献类型:期刊文献
英文题名:Chromosome microdissection, cloning and painting of the chromosome 1 in poplar (Populus tremula)
作者:Zhang, Y.[1] Zhang, S.G.[2] Qi, L.W.[2] Liu, B.[1] Gao, J.M.[1] Chen, C.B.[1] Li, X.L.[1] Song, W.Q.[1]
第一作者:Zhang, Y.
通信作者:Song, W.Q.
机构:[1] Laboratory of Cell Biology, College of Life Sciences, Nankai University, Tianjin 300071, China; [2] Laboratory of Cell Biology, Research Institute of Forestry, Chinese Academy of Forestry, Beijing 100091, China
年份:2005
卷号:54
期号:4-5
起止页码:211-217
外文期刊名:Silvae Genetica
收录:EI(收录号:2005529617074);Scopus(收录号:2-s2.0-29244451088)
语种:英文
外文关键词:Cloning - DNA - Fluorescence - Genes - Plants (botany)
摘要:The chromosome microdissection, cloning and painting technology has evolved into an efficient tool for genomic research. Application of these techniques has rarely been applied for forest plants, largely due to the difficulty of chromosome preparation. The present study was performed to establish a method for single chromosome microdissection, cloning and painting in forest plants using poplar (Populus tremula) as a model. An individual chromosome 1 was microdissected from the metaphase spreads of poplar root-tip cells with fine glass needle controlled by a micromanipulator. The dissected chromosome was amplified in vitro by the Sau3A linker adaptor mediated PCR (LA-PCR) technique, by which 200bp to 3,000bp smear DNA fragments were obtained. Then, the second round PCR products from the single chromosome 1 were cloned into T-easy vectors to generate a DNA library of the chromosome 1. Approximately 3 × 10 5 recombinant clones were obtained. The second round PCR products were used as a complex probe mixture for fluorescent in situ hybridization (FISH) on the metaphase spreads of poplar. Hybridization signals were observed, mainly, along the entire chromosome 1, at the same time, signals were also present on telomeric and centromeric regions of other chromosomes. Therefore, this research suggests that chromosome microdissection, cloning and painting of the single small chromosome in forest plants are feasible.
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