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Construction and Identification of Bacterial Artificial Chromosome Library for 0‐613‐2R in Upland Cotton
Author(s) -
Yin JianMei,
Guo WangZhen,
Zhang TianZhen
Publication year - 2006
Publication title -
journal of integrative plant biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.734
H-Index - 83
eISSN - 1744-7909
pISSN - 1672-9072
DOI - 10.1111/j.1744-7909.2006.00169.x-i1
Subject(s) - bacterial artificial chromosome , insert (composites) , biology , genomic library , genome , genetics , cloning (programming) , library , clone (java method) , genomic dna , positional cloning , chromosome , gene , contig , sequence tagged site , genome size , gene mapping , 16s ribosomal rna , mechanical engineering , computer science , engineering , base sequence , programming language , mutant
A bacterial artificial chromosome (BAC) library containing a large genomic DNA insert is an important tool for genome physical mapping, map‐based cloning, and genome sequencing. To isolate genes via a map‐based cloning strategy and to perform physical mapping of the cotton genome, a high‐quality BAC library containing large cotton DNA inserts is needed. We have developed a BAC library of the restoring line 0‐613‐2R for isolating the fertility restorer (Rf1) gene and genomic research in cotton (Gossypium hirsutum L.). The BAC library contains 97 825 clones stored in 255 pieces of a 384‐well microtiter plate. Random samples of BACs digested with the NotI enzyme indicated that the average insert size is approximately 130 kb, with a range of 80–275 kb, and 95.7% of the BAC clones in the library have an average insert size larger than 100 kb. Based on a cotton genome size of 2 250 Mb, library coverage is 5.7 × haploid genome equivalents. Four clones were selected randomly from the library to determine the stability of the BAC clones. There were no different fingerprints for 0 and 100 generations of each clone digested with NotI and HindIII enzymes. Thus, the stability of a single BAC clone can be sustained at least for 100 generations. Eight simple sequence repeat (SSR) markers flanking the Rf 1 gene were chosen to screen the BAC library by pool using PCR method and 25 positive clones were identified with 3.1 positive clones per SSR marker. (Managing editor: Li‐Hui Zhao)