Evidence map›Paper›PMID 39980057›Full record

ArticleMolecular cytogenetics2025

Preparing high-quality chromosome spreads from Crocus species for karyotyping and FISH.

Abdullah El-Nagish, Susan Liedtke, Sarah Breitenbach, Tony Heitkam

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Article in Molecular cytogenetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 authors.

Abdullah El-NagishDepartment of Biology, Institute of Biology I, RWTH Aachen University, Worringer Weg 3, 52074, Aachen, Germany.ORCID http://orcid.org/0000-0002-5704-5475
Susan LiedtkeFaculty of Biology, Institute of Botany, Technische Universität Dresden, 01069, Dresden, Germany.
Sarah BreitenbachFaculty of Biology, Institute of Botany, Technische Universität Dresden, 01069, Dresden, Germany.
Tony HeitkamDepartment of Biology, Institute of Biology I, RWTH Aachen University, Worringer Weg 3, 52074, Aachen, Germany. tony.heitkam@rwth-aachen.de.ORCID http://orcid.org/0000-0003-0168-8428

Funding

Deutsche Forschungsgemeinschaft 433081887Ministry of Higher Education Call 2019-2020
6 · The paper itself

Abstract

backgroundThe saffron-producing Crocus sativus (L.) and its wild relative C. cartwrightianus (Herb.) are key species for understanding genetic evolution in this genus. Molecular-cytogenetic methods, especially fluorescent in situ hybridization (FISH), are essential for exploring the genetic relationships in this genus. Yet, preparing high-quality chromosomes for FISH analysis across Crocus species remains difficult. A standardized protocol for achieving clear and well-separated mitotic chromosomes is still lacking. This study aimed to assess the effectiveness of pretreatments with four chromosome synchronization methods for optimal chromosome spread preparation in Crocus. Root tips of different Crocus species were treated with four chromosome preparation methods namely hydroxyurea-colchicine (HC), nitrous oxide (NO), hydroxyquinoline (HQ), and ice water (IW) pretreatments to investigate their effectiveness in producing high-quality mitotic chromosome spreads. Metaphases obtained by the four methods were analyzed to assess their quality and metaphase index.

resultsEvaluation of 22,507 cells allowed us to confidently recommend a protocol for Crocus chromosome preparation. Among the methods, ice water pretreatment yielded the highest metaphase index (2.05%), more than doubling the results of HC (1.08%), NO (1.15%), and HQ (1.16%). Ice water-treated chromosomes exhibited better chromosome morphology, with relatively proper size, and non-overlapping chromosomes that were optimal for FISH analysis. Ice water pretreatment was also applied to C. cartwrightianus, the diploid progenitor of C. sativus, where it demonstrated similar efficacy. DAPI staining of chromosomes in both species allowed for clear visualization of intercalary and terminal heterochromatin. FISH analysis using 18S-5.8S-25S and 5S rDNA probes confirmed the utility of IW-prepared chromosome spreads for cytogenetic studies.

conclusionsWe strongly recommend ice water pretreatment as a suitable and effective method for obtaining many metaphase spreads of high-quality in C. sativus and related species, particularly for applications involving a detailed cytogenetic analysis.

Indexed as

Crocus sativusFluorescent in situhybridizationHydroxyquinolineHydroxyurea-colchicine methodIce Water pretreatmentMetaphase indexNitrous oxideSaffron

Identifiers

PMID39980057
PMCPMC11843997

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