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Construction and Characterization of a Bacterial Artificial Chromosome Library for the Hexaploid Wheat Line 92R137

For map-based cloning of genes conferring important traits in the hexaploid wheat line 92R137, a bacterial artificial chromosome (BAC) library, including two sublibraries, was constructed using the genomic DNA of 92R137 digested with restriction enzymes HindIII and BamHI. The BAC library was compose...

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Autores principales: Zeng, Qingdong, Yuan, Fengping, Xu, Xin, Shi, Xue, Nie, Xiaojun, Zhuang, Hua, Chen, Xianming, Wang, Zhonghua, Wang, Xiaojie, Huang, Lili, Han, Dejun, Kang, Zhensheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026951/
https://www.ncbi.nlm.nih.gov/pubmed/24895618
http://dx.doi.org/10.1155/2014/845806
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author Zeng, Qingdong
Yuan, Fengping
Xu, Xin
Shi, Xue
Nie, Xiaojun
Zhuang, Hua
Chen, Xianming
Wang, Zhonghua
Wang, Xiaojie
Huang, Lili
Han, Dejun
Kang, Zhensheng
author_facet Zeng, Qingdong
Yuan, Fengping
Xu, Xin
Shi, Xue
Nie, Xiaojun
Zhuang, Hua
Chen, Xianming
Wang, Zhonghua
Wang, Xiaojie
Huang, Lili
Han, Dejun
Kang, Zhensheng
author_sort Zeng, Qingdong
collection PubMed
description For map-based cloning of genes conferring important traits in the hexaploid wheat line 92R137, a bacterial artificial chromosome (BAC) library, including two sublibraries, was constructed using the genomic DNA of 92R137 digested with restriction enzymes HindIII and BamHI. The BAC library was composed of total 765,696 clones, of which 390,144 were from the HindIII digestion and 375,552 from the BamHI digestion. Through pulsed-field gel electrophoresis (PFGE) analysis of 453 clones randomly selected from the HindIII sublibrary and 573 clones from the BamHI sublibrary, the average insert sizes were estimated as 129 and 113 kb, respectively. Thus, the HindIII sublibrary was estimated to have a 3.01-fold coverage and the BamHI sublibrary a 2.53-fold coverage based on the estimated hexaploid wheat genome size of 16,700 Mb. The 765,696 clones were arrayed in 1,994 384-well plates. All clones were also arranged into plate pools and further arranged into 5-dimensional (5D) pools. The probability of identifying a clone corresponding to any wheat DNA sequence (such as gene Yr26 for stripe rust resistance) from the library was estimated to be more than 99.6%. Through polymerase chain reaction screening the 5D pools with Xwe173, a marker tightly linked to Yr26, six BAC clones were successfully obtained. These results demonstrate that the BAC library is a valuable genomic resource for positional cloning of Yr26 and other genes of interest.
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spelling pubmed-40269512014-06-03 Construction and Characterization of a Bacterial Artificial Chromosome Library for the Hexaploid Wheat Line 92R137 Zeng, Qingdong Yuan, Fengping Xu, Xin Shi, Xue Nie, Xiaojun Zhuang, Hua Chen, Xianming Wang, Zhonghua Wang, Xiaojie Huang, Lili Han, Dejun Kang, Zhensheng Biomed Res Int Research Article For map-based cloning of genes conferring important traits in the hexaploid wheat line 92R137, a bacterial artificial chromosome (BAC) library, including two sublibraries, was constructed using the genomic DNA of 92R137 digested with restriction enzymes HindIII and BamHI. The BAC library was composed of total 765,696 clones, of which 390,144 were from the HindIII digestion and 375,552 from the BamHI digestion. Through pulsed-field gel electrophoresis (PFGE) analysis of 453 clones randomly selected from the HindIII sublibrary and 573 clones from the BamHI sublibrary, the average insert sizes were estimated as 129 and 113 kb, respectively. Thus, the HindIII sublibrary was estimated to have a 3.01-fold coverage and the BamHI sublibrary a 2.53-fold coverage based on the estimated hexaploid wheat genome size of 16,700 Mb. The 765,696 clones were arrayed in 1,994 384-well plates. All clones were also arranged into plate pools and further arranged into 5-dimensional (5D) pools. The probability of identifying a clone corresponding to any wheat DNA sequence (such as gene Yr26 for stripe rust resistance) from the library was estimated to be more than 99.6%. Through polymerase chain reaction screening the 5D pools with Xwe173, a marker tightly linked to Yr26, six BAC clones were successfully obtained. These results demonstrate that the BAC library is a valuable genomic resource for positional cloning of Yr26 and other genes of interest. Hindawi Publishing Corporation 2014 2014-05-05 /pmc/articles/PMC4026951/ /pubmed/24895618 http://dx.doi.org/10.1155/2014/845806 Text en Copyright © 2014 Qingdong Zeng et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zeng, Qingdong
Yuan, Fengping
Xu, Xin
Shi, Xue
Nie, Xiaojun
Zhuang, Hua
Chen, Xianming
Wang, Zhonghua
Wang, Xiaojie
Huang, Lili
Han, Dejun
Kang, Zhensheng
Construction and Characterization of a Bacterial Artificial Chromosome Library for the Hexaploid Wheat Line 92R137
title Construction and Characterization of a Bacterial Artificial Chromosome Library for the Hexaploid Wheat Line 92R137
title_full Construction and Characterization of a Bacterial Artificial Chromosome Library for the Hexaploid Wheat Line 92R137
title_fullStr Construction and Characterization of a Bacterial Artificial Chromosome Library for the Hexaploid Wheat Line 92R137
title_full_unstemmed Construction and Characterization of a Bacterial Artificial Chromosome Library for the Hexaploid Wheat Line 92R137
title_short Construction and Characterization of a Bacterial Artificial Chromosome Library for the Hexaploid Wheat Line 92R137
title_sort construction and characterization of a bacterial artificial chromosome library for the hexaploid wheat line 92r137
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026951/
https://www.ncbi.nlm.nih.gov/pubmed/24895618
http://dx.doi.org/10.1155/2014/845806
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