Construction of a bacterial artificial chromosome (BAC) library for citrus and identification of BAC contigs containing resistance gene candidates

被引:0
|
作者
Z. Deng
Q. Tao
Y.-L. Chang
S. Huang
P. Ling
C. Yu
C. Chen
F. G. Gmitter Jr.
H.-B. Zhang
机构
[1] University of Florida,
[2] Citrus Research and Education Center,undefined
[3] 700 Experiment Station Road,undefined
[4] Lake Alfred,undefined
[5] FL 33850,undefined
[6] USA e-mail: fgg@lal.ufl.edu Fax: +1-863-9564631,undefined
[7] Texas A&M University,undefined
[8] Department of Soil and Crop Sciences and Crop Biotechnology Center,undefined
[9] College Station,undefined
[10] TX 77843,undefined
[11] USA,undefined
来源
Theoretical and Applied Genetics | 2001年 / 102卷
关键词
Keywords Citrus; BAC library; CTV resistance gene; Resistance gene candidates;
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中图分类号
学科分类号
摘要
A BAC library was constructed from the genomic DNA of an intergeneric Citrus and Poncirus hybrid. The library consists of 24,576 clones with an average insert size of 115 kb, representing approximately seven haploid genome equivalents and is able to give a greater than 99% probability of isolating single-copy citrus DNA sequences from this library. High-density colony hybridization-based library screening was performed using DNA markers linked to the citrus tristeza virus (CTV) resistance gene and citrus disease resistance gene candidate (RGC) sequences. Between four and eight clones were isolated with each of the CTV resistance gene-linked markers, which agrees with the library’s predicted genome coverage. Three hundred and twenty-two clones were identified using 13 previously cloned citrus RGC sequences as probes in library screening. One to four fragments in each BAC were shown to hybridize with RGC sequences. One hundred and nine of the RGC BAC clones were fingerprinted using a sequencing gel-based procedure. From the fingerprints, 25 contigs were assembled, each having a size of 120–250 kb and consisting of 2–11 clones. These results indicate that the library is a useful resource for BAC contig construction and molecular isolation of disease resistance genes.
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页码:1177 / 1184
页数:7
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