Karyotyping of commercial cultivars of melon (Cucumis melo L.)

Background This study on cultivars of melon ( Cucumis melo L.) marketed in Brazil was conducted to obtain information to be used in breeding programs of this species. Little is known about the karyotype variability among C. melo L. cultivars targeted at the consumer market. The objective of the pres...

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Veröffentlicht in:Molecular biology reports 2022-11, Vol.49 (11), p.10279-10292
Hauptverfasser: Santos, Matusalem Campos, Souza, Margarete Magalhães, de Melo, Cláusio Antônio Ferreira, Silva, Gonçalo Santos
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container_end_page 10292
container_issue 11
container_start_page 10279
container_title Molecular biology reports
container_volume 49
creator Santos, Matusalem Campos
Souza, Margarete Magalhães
de Melo, Cláusio Antônio Ferreira
Silva, Gonçalo Santos
description Background This study on cultivars of melon ( Cucumis melo L.) marketed in Brazil was conducted to obtain information to be used in breeding programs of this species. Little is known about the karyotype variability among C. melo L. cultivars targeted at the consumer market. The objective of the present study was to verify the karyotype variability in eight commercial melon cultivars used in the Brazilian market. Methods and results Slides were stained with 2% Giemsa and assembled with Neomount to perform chromosomal morphometry. GC-rich heterochromatin was observed by CMA 3 /DAPI staining. 5 S rDNA, centromeric satellite DNA (SatDNA), and telomeric sites were visualized using fluorescence in situ hybridization. All images were captured on an Olympus BX41 microscope equipped with a 5 M Olympus DP25 digital camera and DP2-BSW software. The cultivars showed symmetrical karyotypes with significant differences in total chromosome length and average chromosome size. Heterochromatic CMA 3 + blocks were observed in terminal regions related to satellites (secondary constrictions), as well as in centromeric and pericentromeric regions. A single chromosomal pair of 5 S rDNA sites was observed in all cultivars, but at distinct locations. Centromeric satellite sequences, tested for the first time in melon, revealed only centromeric sites. Telomeric sites were observed in all the chromosomes of the cultivars. Conclusions Karyotype variation was observed in cultivars of melon, which were analyzed for chromosomal morphology and localization of GC-rich heterochromatin, as well centromeric SatDNA, rDNA, and telomeric chromosomal markers. Hence, these cultivars can be used in future breeding programs.
doi_str_mv 10.1007/s11033-022-07520-z
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Little is known about the karyotype variability among C. melo L. cultivars targeted at the consumer market. The objective of the present study was to verify the karyotype variability in eight commercial melon cultivars used in the Brazilian market. Methods and results Slides were stained with 2% Giemsa and assembled with Neomount to perform chromosomal morphometry. GC-rich heterochromatin was observed by CMA 3 /DAPI staining. 5 S rDNA, centromeric satellite DNA (SatDNA), and telomeric sites were visualized using fluorescence in situ hybridization. All images were captured on an Olympus BX41 microscope equipped with a 5 M Olympus DP25 digital camera and DP2-BSW software. The cultivars showed symmetrical karyotypes with significant differences in total chromosome length and average chromosome size. Heterochromatic CMA 3 + blocks were observed in terminal regions related to satellites (secondary constrictions), as well as in centromeric and pericentromeric regions. A single chromosomal pair of 5 S rDNA sites was observed in all cultivars, but at distinct locations. Centromeric satellite sequences, tested for the first time in melon, revealed only centromeric sites. Telomeric sites were observed in all the chromosomes of the cultivars. Conclusions Karyotype variation was observed in cultivars of melon, which were analyzed for chromosomal morphology and localization of GC-rich heterochromatin, as well centromeric SatDNA, rDNA, and telomeric chromosomal markers. Hence, these cultivars can be used in future breeding programs.</description><identifier>ISSN: 0301-4851</identifier><identifier>EISSN: 1573-4978</identifier><identifier>DOI: 10.1007/s11033-022-07520-z</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Animal Anatomy ; Animal Biochemistry ; Biomedical and Life Sciences ; Chromosomes ; Cucumis melo ; Cultivars ; Fluorescence in situ hybridization ; Heterochromatin ; Histology ; Karyotypes ; Life Sciences ; Localization ; Morphology ; Morphometry ; Original Article ; Plant breeding ; Satellite DNA ; Satellites</subject><ispartof>Molecular biology reports, 2022-11, Vol.49 (11), p.10279-10292</ispartof><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2022</rights><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2022.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c282t-5b32eb3438c4842f7a488f5c606c73b8f2124491388b126a007534721ba739493</citedby><cites>FETCH-LOGICAL-c282t-5b32eb3438c4842f7a488f5c606c73b8f2124491388b126a007534721ba739493</cites><orcidid>0000-0003-0292-7988</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11033-022-07520-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11033-022-07520-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27922,27923,41486,42555,51317</link.rule.ids></links><search><creatorcontrib>Santos, Matusalem Campos</creatorcontrib><creatorcontrib>Souza, Margarete Magalhães</creatorcontrib><creatorcontrib>de Melo, Cláusio Antônio Ferreira</creatorcontrib><creatorcontrib>Silva, Gonçalo Santos</creatorcontrib><title>Karyotyping of commercial cultivars of melon (Cucumis melo L.)</title><title>Molecular biology reports</title><addtitle>Mol Biol Rep</addtitle><description>Background This study on cultivars of melon ( Cucumis melo L.) marketed in Brazil was conducted to obtain information to be used in breeding programs of this species. Little is known about the karyotype variability among C. melo L. cultivars targeted at the consumer market. The objective of the present study was to verify the karyotype variability in eight commercial melon cultivars used in the Brazilian market. Methods and results Slides were stained with 2% Giemsa and assembled with Neomount to perform chromosomal morphometry. GC-rich heterochromatin was observed by CMA 3 /DAPI staining. 5 S rDNA, centromeric satellite DNA (SatDNA), and telomeric sites were visualized using fluorescence in situ hybridization. All images were captured on an Olympus BX41 microscope equipped with a 5 M Olympus DP25 digital camera and DP2-BSW software. The cultivars showed symmetrical karyotypes with significant differences in total chromosome length and average chromosome size. Heterochromatic CMA 3 + blocks were observed in terminal regions related to satellites (secondary constrictions), as well as in centromeric and pericentromeric regions. A single chromosomal pair of 5 S rDNA sites was observed in all cultivars, but at distinct locations. Centromeric satellite sequences, tested for the first time in melon, revealed only centromeric sites. Telomeric sites were observed in all the chromosomes of the cultivars. Conclusions Karyotype variation was observed in cultivars of melon, which were analyzed for chromosomal morphology and localization of GC-rich heterochromatin, as well centromeric SatDNA, rDNA, and telomeric chromosomal markers. 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Souza, Margarete Magalhães ; de Melo, Cláusio Antônio Ferreira ; Silva, Gonçalo Santos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c282t-5b32eb3438c4842f7a488f5c606c73b8f2124491388b126a007534721ba739493</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animal Anatomy</topic><topic>Animal Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Chromosomes</topic><topic>Cucumis melo</topic><topic>Cultivars</topic><topic>Fluorescence in situ hybridization</topic><topic>Heterochromatin</topic><topic>Histology</topic><topic>Karyotypes</topic><topic>Life Sciences</topic><topic>Localization</topic><topic>Morphology</topic><topic>Morphometry</topic><topic>Original Article</topic><topic>Plant breeding</topic><topic>Satellite DNA</topic><topic>Satellites</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Santos, Matusalem Campos</creatorcontrib><creatorcontrib>Souza, Margarete Magalhães</creatorcontrib><creatorcontrib>de Melo, Cláusio Antônio Ferreira</creatorcontrib><creatorcontrib>Silva, Gonçalo Santos</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health &amp; 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Little is known about the karyotype variability among C. melo L. cultivars targeted at the consumer market. The objective of the present study was to verify the karyotype variability in eight commercial melon cultivars used in the Brazilian market. Methods and results Slides were stained with 2% Giemsa and assembled with Neomount to perform chromosomal morphometry. GC-rich heterochromatin was observed by CMA 3 /DAPI staining. 5 S rDNA, centromeric satellite DNA (SatDNA), and telomeric sites were visualized using fluorescence in situ hybridization. All images were captured on an Olympus BX41 microscope equipped with a 5 M Olympus DP25 digital camera and DP2-BSW software. The cultivars showed symmetrical karyotypes with significant differences in total chromosome length and average chromosome size. Heterochromatic CMA 3 + blocks were observed in terminal regions related to satellites (secondary constrictions), as well as in centromeric and pericentromeric regions. A single chromosomal pair of 5 S rDNA sites was observed in all cultivars, but at distinct locations. Centromeric satellite sequences, tested for the first time in melon, revealed only centromeric sites. Telomeric sites were observed in all the chromosomes of the cultivars. Conclusions Karyotype variation was observed in cultivars of melon, which were analyzed for chromosomal morphology and localization of GC-rich heterochromatin, as well centromeric SatDNA, rDNA, and telomeric chromosomal markers. Hence, these cultivars can be used in future breeding programs.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s11033-022-07520-z</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0003-0292-7988</orcidid></addata></record>
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subjects Animal Anatomy
Animal Biochemistry
Biomedical and Life Sciences
Chromosomes
Cucumis melo
Cultivars
Fluorescence in situ hybridization
Heterochromatin
Histology
Karyotypes
Life Sciences
Localization
Morphology
Morphometry
Original Article
Plant breeding
Satellite DNA
Satellites
title Karyotyping of commercial cultivars of melon (Cucumis melo L.)
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