Evidence map›Paper›PMID 23374863›Full record

ArticleMolecular cytogenetics2013

Generation of multicolor banding probes for chromosomes of different species.

Nadezda Kosyakova, Ahmed Basheer Hamid, Arunrat Chaveerach, Krit Pinthong, Pornnarong Siripiyasing, Weerayuth Supiwong, Svetlana Romanenko, Vladimir Trifonov, Xiaobo Fan

Abstract read
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Article in Molecular cytogenetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Cellular and genomic approaches for exploring structural chromosomal rearrangements.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2020
    Review
  4. Article
  5. Molecular Cytogenetic Characterization Identified the Murine B-Cell Lymphoma Cell Line A-20 as a Model for Sporadic Burkitt's Lymphoma.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2017
    Article
  6. Article
  7. Article
  8. Article
  9. Article
4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Nadezda KosyakovaJena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Kollegiengasse 10, Jena, D-07743, Germany. Nadezda.Kosyakova@mti.uni-jena.de.
Ahmed Basheer Hamid
Arunrat Chaveerach
Krit Pinthong
Pornnarong Siripiyasing
Weerayuth Supiwong
Svetlana Romanenko
Vladimir Trifonov
Xiaobo Fan

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelled

backgroundThe 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.

resultsHere 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

conclusionsThe 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.

Identifiers

PMID23374863
PMCPMC3575270

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.