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以柚(Citrus grandis)为模型对染色体较小的木本果树单条染色体进行显微切割和分子操作。I. 单条染色体DNA文库的构建。

Microdissection and molecular manipulation of single chromosomes in woody fruit trees with small chromosomes using pomelo (Citrus grandis) as a model. I. Construction of single chromosomal DNA libraries.

作者信息

Huang D, Wu W, Zhou Y, Hu Z, Lu L

机构信息

College of horticulture, Fujian Agriculture and Forestry University, 350002, Fuzhou, P.R. China.

出版信息

Theor Appl Genet. 2004 May;108(7):1366-70. doi: 10.1007/s00122-003-1550-3. Epub 2004 Jan 16.

Abstract

Construction of single chromosomal DNA libraries by means of chromosome microdissection and microcloning will be useful for genomic research, especially for those species that have not been extensively studied genetically. Application of the technology of microdissection and microcloning to woody fruit plants has not been reported hitherto, largely due to the generally small sizes of metaphase chromosomes and the difficulty of chromosome preparation. The present study was performed to establish a method for single chromosome microdissection and microcloning in woody fruit species using pomelo as a model. The standard karyotype of a pomelo cultivar ( Citrus grandis cv. Guanxi) was established based on 20 prometaphase photomicrographs. According to the standard karyotype, chromosome 1 was identified and isolated with fine glass microneedles controlled by a micromanipulator. DNA fragments ranging from 0.3 kb to 2 kb were acquired from the isolated single chromosome 1 via two rounds of PCR mediated by Sau3A linker adaptors and then cloned into T-easy vectors to generate a DNA library of chromosome 1. Approximately 30,000 recombinant clones were obtained. Evaluation based on 108 randomly selected clones showed that the sizes of the cloned inserts varied from 0.5 kb to 1.5 kb with an average of 860 bp. Our research suggests that microdissection and microcloning of single small chromosomes in woody plants is feasible.

摘要

通过染色体显微切割和微克隆构建单条染色体DNA文库,将有助于基因组研究,特别是对于那些尚未进行广泛遗传研究的物种。迄今尚未见将显微切割和微克隆技术应用于木本果树植物的报道,这主要是由于中期染色体通常较小以及染色体标本制备困难。本研究以柚为模式,旨在建立木本果树单条染色体显微切割和微克隆的方法。基于20张早中期显微照片建立了一个柚品种(琯溪蜜柚)的标准核型。根据标准核型,用显微操作仪控制的精细玻璃微针鉴定并分离出1号染色体。通过Sau3A接头介导的两轮PCR从分离的单条1号染色体中获得了0.3 kb至2 kb的DNA片段,然后将其克隆到T - easy载体中,构建了1号染色体的DNA文库。共获得约30000个重组克隆。对随机选取的108个克隆进行评估表明,克隆插入片段的大小在0.5 kb至1.5 kb之间,平均为860 bp。我们的研究表明,木本植物单条小染色体的显微切割和微克隆是可行的。

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