Identification and mapping of simple sequence repeat markers from common bean (phaseolus vulgaris l.) bacterial artificial chromosome end sequences for genome characterization and genetic-physical map integration

Microsatellite markers or simple sequence repeat (SSR) loci are useful for diversity characterization and genetic?physical mapping. Different in silico microsatellite search methods have been developed for mining bacterial artificial chromosome (BAC) end sequences for SSRs. The overall goal of this study was genome characterization based on SSRs in 89,017 BAC end sequences (BESs) from the G19833 common bean (Phaseolus vulgaris L.) library. Another objective was to identify new SSR taking into account three tandem motif identification programs (Automated Microsatellite Marker Development [AMMD], Tandem Repeats Finder [TRF], and SSRLocator [SSRL]). Among the microsatellite search engines, SSRL identified the highest number of SSRs; however, when primer design was attempted, the number dropped due to poor primer design regions. Automated Microsatellite Marker Development software identified many SSRs with valuable AT/TA or AG/TC motifs, while TRF found fewer SSRs and produced no primers. A subgroup of 323 AT-rich, di-, and trinucleotide SSRs were selected from the AMMD results and used in a parental survey with DOR364 and G19833, of which 75 could be mapped in the corresponding population; these represented 4052 BAC clones. Together with 92 previously mapped BES- and 114 non-BES-derived markers, a total of 280 SSRs were included in the polymerase chain reaction (PCR)-based map, integrating a total of 8232 BAC clones in 162 contigs from the physical map.

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Main Authors: Cordoba, J.M., Chavarro, C., Rojas, F., Muñoz, C., Blair, M.W.
Format: Article biblioteca
Language:English
Published: Crop Science Society of America 2010
Subjects:AGRICULTURAL SCIENCES AND BIOTECHNOLOGY, MICROSATELLITES, PHASEOLUS VULGARIS, PCR, GENETIC MAPS,
Online Access:http://hdl.handle.net/10883/1845
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spelling dig-cimmyt-10883-18452021-02-09T20:59:00Z Identification and mapping of simple sequence repeat markers from common bean (phaseolus vulgaris l.) bacterial artificial chromosome end sequences for genome characterization and genetic-physical map integration Cordoba, J.M. Chavarro, C. Rojas, F. Muñoz, C. Blair, M.W. AGRICULTURAL SCIENCES AND BIOTECHNOLOGY MICROSATELLITES PHASEOLUS VULGARIS PCR GENETIC MAPS Microsatellite markers or simple sequence repeat (SSR) loci are useful for diversity characterization and genetic?physical mapping. Different in silico microsatellite search methods have been developed for mining bacterial artificial chromosome (BAC) end sequences for SSRs. The overall goal of this study was genome characterization based on SSRs in 89,017 BAC end sequences (BESs) from the G19833 common bean (Phaseolus vulgaris L.) library. Another objective was to identify new SSR taking into account three tandem motif identification programs (Automated Microsatellite Marker Development [AMMD], Tandem Repeats Finder [TRF], and SSRLocator [SSRL]). Among the microsatellite search engines, SSRL identified the highest number of SSRs; however, when primer design was attempted, the number dropped due to poor primer design regions. Automated Microsatellite Marker Development software identified many SSRs with valuable AT/TA or AG/TC motifs, while TRF found fewer SSRs and produced no primers. A subgroup of 323 AT-rich, di-, and trinucleotide SSRs were selected from the AMMD results and used in a parental survey with DOR364 and G19833, of which 75 could be mapped in the corresponding population; these represented 4052 BAC clones. Together with 92 previously mapped BES- and 114 non-BES-derived markers, a total of 280 SSRs were included in the polymerase chain reaction (PCR)-based map, integrating a total of 8232 BAC clones in 162 contigs from the physical map. 154-165 2013-06-07T21:02:47Z 2013-06-07T21:02:47Z 2010 Article 1940-3372 http://hdl.handle.net/10883/1845 10.3835/plantgenome2010.06.0013 English Open Access PDF Crop Science Society of America 3 3 The Plant Genome
institution CIMMYT
collection DSpace
country México
countrycode MX
component Bibliográfico
access En linea
databasecode dig-cimmyt
tag biblioteca
region America del Norte
libraryname CIMMYT Library
language English
topic AGRICULTURAL SCIENCES AND BIOTECHNOLOGY
MICROSATELLITES
PHASEOLUS VULGARIS
PCR
GENETIC MAPS
AGRICULTURAL SCIENCES AND BIOTECHNOLOGY
MICROSATELLITES
PHASEOLUS VULGARIS
PCR
GENETIC MAPS
spellingShingle AGRICULTURAL SCIENCES AND BIOTECHNOLOGY
MICROSATELLITES
PHASEOLUS VULGARIS
PCR
GENETIC MAPS
AGRICULTURAL SCIENCES AND BIOTECHNOLOGY
MICROSATELLITES
PHASEOLUS VULGARIS
PCR
GENETIC MAPS
Cordoba, J.M.
Chavarro, C.
Rojas, F.
Muñoz, C.
Blair, M.W.
Identification and mapping of simple sequence repeat markers from common bean (phaseolus vulgaris l.) bacterial artificial chromosome end sequences for genome characterization and genetic-physical map integration
description Microsatellite markers or simple sequence repeat (SSR) loci are useful for diversity characterization and genetic?physical mapping. Different in silico microsatellite search methods have been developed for mining bacterial artificial chromosome (BAC) end sequences for SSRs. The overall goal of this study was genome characterization based on SSRs in 89,017 BAC end sequences (BESs) from the G19833 common bean (Phaseolus vulgaris L.) library. Another objective was to identify new SSR taking into account three tandem motif identification programs (Automated Microsatellite Marker Development [AMMD], Tandem Repeats Finder [TRF], and SSRLocator [SSRL]). Among the microsatellite search engines, SSRL identified the highest number of SSRs; however, when primer design was attempted, the number dropped due to poor primer design regions. Automated Microsatellite Marker Development software identified many SSRs with valuable AT/TA or AG/TC motifs, while TRF found fewer SSRs and produced no primers. A subgroup of 323 AT-rich, di-, and trinucleotide SSRs were selected from the AMMD results and used in a parental survey with DOR364 and G19833, of which 75 could be mapped in the corresponding population; these represented 4052 BAC clones. Together with 92 previously mapped BES- and 114 non-BES-derived markers, a total of 280 SSRs were included in the polymerase chain reaction (PCR)-based map, integrating a total of 8232 BAC clones in 162 contigs from the physical map.
format Article
topic_facet AGRICULTURAL SCIENCES AND BIOTECHNOLOGY
MICROSATELLITES
PHASEOLUS VULGARIS
PCR
GENETIC MAPS
author Cordoba, J.M.
Chavarro, C.
Rojas, F.
Muñoz, C.
Blair, M.W.
author_facet Cordoba, J.M.
Chavarro, C.
Rojas, F.
Muñoz, C.
Blair, M.W.
author_sort Cordoba, J.M.
title Identification and mapping of simple sequence repeat markers from common bean (phaseolus vulgaris l.) bacterial artificial chromosome end sequences for genome characterization and genetic-physical map integration
title_short Identification and mapping of simple sequence repeat markers from common bean (phaseolus vulgaris l.) bacterial artificial chromosome end sequences for genome characterization and genetic-physical map integration
title_full Identification and mapping of simple sequence repeat markers from common bean (phaseolus vulgaris l.) bacterial artificial chromosome end sequences for genome characterization and genetic-physical map integration
title_fullStr Identification and mapping of simple sequence repeat markers from common bean (phaseolus vulgaris l.) bacterial artificial chromosome end sequences for genome characterization and genetic-physical map integration
title_full_unstemmed Identification and mapping of simple sequence repeat markers from common bean (phaseolus vulgaris l.) bacterial artificial chromosome end sequences for genome characterization and genetic-physical map integration
title_sort identification and mapping of simple sequence repeat markers from common bean (phaseolus vulgaris l.) bacterial artificial chromosome end sequences for genome characterization and genetic-physical map integration
publisher Crop Science Society of America
publishDate 2010
url http://hdl.handle.net/10883/1845
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