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Generation of multicolor banding probes for chromosomes of different species

BACKGROUND: The multicolor banding (MCB/mBAND) technique provides a unique opportunity to characterize intrachromosomal rearrangements and to determine chromosomal breakpoints. Until recently, MCB probes have only been available for human and some murine chromosomes. Generation of MCB probes for chr...

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Autores principales: Kosyakova, Nadezda, Hamid, Ahmed Basheer, Chaveerach, Arunrat, Pinthong, Krit, Siripiyasing, Pornnarong, Supiwong, Weerayuth, Romanenko, Svetlana, Trifonov, Vladimir, Fan, Xiaobo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3575270/
https://www.ncbi.nlm.nih.gov/pubmed/23374863
http://dx.doi.org/10.1186/1755-8166-6-6
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author Kosyakova, Nadezda
Hamid, Ahmed Basheer
Chaveerach, Arunrat
Pinthong, Krit
Siripiyasing, Pornnarong
Supiwong, Weerayuth
Romanenko, Svetlana
Trifonov, Vladimir
Fan, Xiaobo
author_facet Kosyakova, Nadezda
Hamid, Ahmed Basheer
Chaveerach, Arunrat
Pinthong, Krit
Siripiyasing, Pornnarong
Supiwong, Weerayuth
Romanenko, Svetlana
Trifonov, Vladimir
Fan, Xiaobo
author_sort Kosyakova, Nadezda
collection PubMed
description BACKGROUND: The multicolor banding (MCB/mBAND) technique provides a unique opportunity to characterize intrachromosomal rearrangements and to determine chromosomal breakpoints. Until recently, MCB probes have only been available for human and some murine chromosomes. Generation of MCB probes for chromosomes of other species, useful and required in many cytogenetics research fields, was limited by technical difficulties. MCB probes are established by chromosome microdissection followed by whole genomic DNA amplification. However, unambiguous identification of the target chromosome is required for MCB-probe establishment. Previously proposed protocols suggested G-banding staining or preliminary FISH with whole chromosome paints (WCP) as methods to identify the chromosome of interest. RESULTS: Here we present a complete workflow for MCB probe generation for those cases and species where chromosome morphology is too challenging to recognize target chromosomes by conventional methods and where WCP probes are not available. The workflow was successfully applied for murine chromosomes that are difficult to identify unambiguously. Additionally, we showed that glass-needle based microdissection enables establishment of a whole set of WCP paints by microdissection of individual chromosomes of a single metaphase CONCLUSIONS: The present method can be applied for generation of whole or region-specific DNA probes for species, where karyotyping of G-banded chromosomes is challenging due to similar chromosome morphology and/or chromosome banding patterns.
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spelling pubmed-35752702013-02-19 Generation of multicolor banding probes for chromosomes of different species Kosyakova, Nadezda Hamid, Ahmed Basheer Chaveerach, Arunrat Pinthong, Krit Siripiyasing, Pornnarong Supiwong, Weerayuth Romanenko, Svetlana Trifonov, Vladimir Fan, Xiaobo Mol Cytogenet Methodology BACKGROUND: The multicolor banding (MCB/mBAND) technique provides a unique opportunity to characterize intrachromosomal rearrangements and to determine chromosomal breakpoints. Until recently, MCB probes have only been available for human and some murine chromosomes. Generation of MCB probes for chromosomes of other species, useful and required in many cytogenetics research fields, was limited by technical difficulties. MCB probes are established by chromosome microdissection followed by whole genomic DNA amplification. However, unambiguous identification of the target chromosome is required for MCB-probe establishment. Previously proposed protocols suggested G-banding staining or preliminary FISH with whole chromosome paints (WCP) as methods to identify the chromosome of interest. RESULTS: Here we present a complete workflow for MCB probe generation for those cases and species where chromosome morphology is too challenging to recognize target chromosomes by conventional methods and where WCP probes are not available. The workflow was successfully applied for murine chromosomes that are difficult to identify unambiguously. Additionally, we showed that glass-needle based microdissection enables establishment of a whole set of WCP paints by microdissection of individual chromosomes of a single metaphase CONCLUSIONS: The present method can be applied for generation of whole or region-specific DNA probes for species, where karyotyping of G-banded chromosomes is challenging due to similar chromosome morphology and/or chromosome banding patterns. BioMed Central 2013-02-04 /pmc/articles/PMC3575270/ /pubmed/23374863 http://dx.doi.org/10.1186/1755-8166-6-6 Text en Copyright ©2013 Kosyakova et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology
Kosyakova, Nadezda
Hamid, Ahmed Basheer
Chaveerach, Arunrat
Pinthong, Krit
Siripiyasing, Pornnarong
Supiwong, Weerayuth
Romanenko, Svetlana
Trifonov, Vladimir
Fan, Xiaobo
Generation of multicolor banding probes for chromosomes of different species
title Generation of multicolor banding probes for chromosomes of different species
title_full Generation of multicolor banding probes for chromosomes of different species
title_fullStr Generation of multicolor banding probes for chromosomes of different species
title_full_unstemmed Generation of multicolor banding probes for chromosomes of different species
title_short Generation of multicolor banding probes for chromosomes of different species
title_sort generation of multicolor banding probes for chromosomes of different species
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3575270/
https://www.ncbi.nlm.nih.gov/pubmed/23374863
http://dx.doi.org/10.1186/1755-8166-6-6
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