Is partial desynapsis in cauliflower (Brassica oleracea L. var. botrytis) pollen mother cells linked to aneuploidy in the crop?
Abstract Trisomic cauliflower plants (Brassica oleracea L. var. botrytis) display abnormal curd phenotypes that seriously decrease commercial value of the crop. Despite extensive breeding efforts, selection of genotypes producing euploid gametes remains unsuccessful due to unknown genetic and enviro...
Ausführliche Beschreibung
Autor*in: |
Ji, Xianwen [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2022 |
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Schlagwörter: |
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Anmerkung: |
© The Author(s) 2022 |
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Übergeordnetes Werk: |
Enthalten in: Euphytica - Dordrecht [u.a.] : Springer Science + Business Media B.V., 1952, 218(2022), 6 vom: 24. Mai |
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Übergeordnetes Werk: |
volume:218 ; year:2022 ; number:6 ; day:24 ; month:05 |
Links: |
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DOI / URN: |
10.1007/s10681-022-03027-7 |
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Katalog-ID: |
SPR047091169 |
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245 | 1 | 0 | |a Is partial desynapsis in cauliflower (Brassica oleracea L. var. botrytis) pollen mother cells linked to aneuploidy in the crop? |
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520 | |a Abstract Trisomic cauliflower plants (Brassica oleracea L. var. botrytis) display abnormal curd phenotypes that seriously decrease commercial value of the crop. Despite extensive breeding efforts, selection of genotypes producing euploid gametes remains unsuccessful due to unknown genetic and environmental factors. To reveal an eventual role of an-euploid gametes, we analyzed chromosome pairing, chiasma formation and chromosome segregation in pollen mother cells of selected cauliflower genotypes. To this end we compared three genotypes exhibiting Low with < 5%, Moderate with 5–10% and High with > 10% aberrant offspring, respectively. Although chromosome pairing at pachytene was regular, cells at diakinesis and metaphase I showed variable numbers of univalents, suggesting partial desynapsis. Cells at anaphase I–telophase II exhibit various degrees of unbalanced chromosome numbers, that may explain the aneuploid offspring. Immunofluorescence probed with an MLH1 antibody demonstrated fluorescent foci in all genotypes, but their lower numbers do not correspond to the number of putative chiasmata. Interchromosomal connections between chromosomes and bivalents are common at diakinesis and metaphase I, and they contain centromeric and 45S rDNA tandem repeats, but such chromatin connections seem not to affect proper disjoin of the half bivalents at anaphase I. Moreover, male meiosis in the Arabidopsis APETALA1/CAULIFLOWER double mutant with the typical cauliflower phenotype does show interchromosomal connections, but there are no indications for partial desynapsis. The causality of the curd development on the desynapsis in cauliflower is still a matter of debate. | ||
650 | 4 | |a Cauliflower |7 (dpeaa)DE-He213 | |
650 | 4 | |a Aneuploidy |7 (dpeaa)DE-He213 | |
650 | 4 | |a Desynapsis |7 (dpeaa)DE-He213 | |
700 | 1 | |a Lelivelt, Cilia |4 aut | |
700 | 1 | |a Wijnker, Erik |4 aut | |
700 | 1 | |a de Jong, Hans |0 (orcid)0000-0003-2262-4941 |4 aut | |
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10.1007/s10681-022-03027-7 doi (DE-627)SPR047091169 (SPR)s10681-022-03027-7-e DE-627 ger DE-627 rakwb eng Ji, Xianwen verfasserin aut Is partial desynapsis in cauliflower (Brassica oleracea L. var. botrytis) pollen mother cells linked to aneuploidy in the crop? 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2022 Abstract Trisomic cauliflower plants (Brassica oleracea L. var. botrytis) display abnormal curd phenotypes that seriously decrease commercial value of the crop. Despite extensive breeding efforts, selection of genotypes producing euploid gametes remains unsuccessful due to unknown genetic and environmental factors. To reveal an eventual role of an-euploid gametes, we analyzed chromosome pairing, chiasma formation and chromosome segregation in pollen mother cells of selected cauliflower genotypes. To this end we compared three genotypes exhibiting Low with < 5%, Moderate with 5–10% and High with > 10% aberrant offspring, respectively. Although chromosome pairing at pachytene was regular, cells at diakinesis and metaphase I showed variable numbers of univalents, suggesting partial desynapsis. Cells at anaphase I–telophase II exhibit various degrees of unbalanced chromosome numbers, that may explain the aneuploid offspring. Immunofluorescence probed with an MLH1 antibody demonstrated fluorescent foci in all genotypes, but their lower numbers do not correspond to the number of putative chiasmata. Interchromosomal connections between chromosomes and bivalents are common at diakinesis and metaphase I, and they contain centromeric and 45S rDNA tandem repeats, but such chromatin connections seem not to affect proper disjoin of the half bivalents at anaphase I. Moreover, male meiosis in the Arabidopsis APETALA1/CAULIFLOWER double mutant with the typical cauliflower phenotype does show interchromosomal connections, but there are no indications for partial desynapsis. The causality of the curd development on the desynapsis in cauliflower is still a matter of debate. Cauliflower (dpeaa)DE-He213 Aneuploidy (dpeaa)DE-He213 Desynapsis (dpeaa)DE-He213 Lelivelt, Cilia aut Wijnker, Erik aut de Jong, Hans (orcid)0000-0003-2262-4941 aut Enthalten in Euphytica Dordrecht [u.a.] : Springer Science + Business Media B.V., 1952 218(2022), 6 vom: 24. Mai (DE-627)312840098 (DE-600)2012322-X 1573-5060 nnns volume:218 year:2022 number:6 day:24 month:05 https://dx.doi.org/10.1007/s10681-022-03027-7 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_211 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 218 2022 6 24 05 |
spelling |
10.1007/s10681-022-03027-7 doi (DE-627)SPR047091169 (SPR)s10681-022-03027-7-e DE-627 ger DE-627 rakwb eng Ji, Xianwen verfasserin aut Is partial desynapsis in cauliflower (Brassica oleracea L. var. botrytis) pollen mother cells linked to aneuploidy in the crop? 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2022 Abstract Trisomic cauliflower plants (Brassica oleracea L. var. botrytis) display abnormal curd phenotypes that seriously decrease commercial value of the crop. Despite extensive breeding efforts, selection of genotypes producing euploid gametes remains unsuccessful due to unknown genetic and environmental factors. To reveal an eventual role of an-euploid gametes, we analyzed chromosome pairing, chiasma formation and chromosome segregation in pollen mother cells of selected cauliflower genotypes. To this end we compared three genotypes exhibiting Low with < 5%, Moderate with 5–10% and High with > 10% aberrant offspring, respectively. Although chromosome pairing at pachytene was regular, cells at diakinesis and metaphase I showed variable numbers of univalents, suggesting partial desynapsis. Cells at anaphase I–telophase II exhibit various degrees of unbalanced chromosome numbers, that may explain the aneuploid offspring. Immunofluorescence probed with an MLH1 antibody demonstrated fluorescent foci in all genotypes, but their lower numbers do not correspond to the number of putative chiasmata. Interchromosomal connections between chromosomes and bivalents are common at diakinesis and metaphase I, and they contain centromeric and 45S rDNA tandem repeats, but such chromatin connections seem not to affect proper disjoin of the half bivalents at anaphase I. Moreover, male meiosis in the Arabidopsis APETALA1/CAULIFLOWER double mutant with the typical cauliflower phenotype does show interchromosomal connections, but there are no indications for partial desynapsis. The causality of the curd development on the desynapsis in cauliflower is still a matter of debate. Cauliflower (dpeaa)DE-He213 Aneuploidy (dpeaa)DE-He213 Desynapsis (dpeaa)DE-He213 Lelivelt, Cilia aut Wijnker, Erik aut de Jong, Hans (orcid)0000-0003-2262-4941 aut Enthalten in Euphytica Dordrecht [u.a.] : Springer Science + Business Media B.V., 1952 218(2022), 6 vom: 24. Mai (DE-627)312840098 (DE-600)2012322-X 1573-5060 nnns volume:218 year:2022 number:6 day:24 month:05 https://dx.doi.org/10.1007/s10681-022-03027-7 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_211 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 218 2022 6 24 05 |
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10.1007/s10681-022-03027-7 doi (DE-627)SPR047091169 (SPR)s10681-022-03027-7-e DE-627 ger DE-627 rakwb eng Ji, Xianwen verfasserin aut Is partial desynapsis in cauliflower (Brassica oleracea L. var. botrytis) pollen mother cells linked to aneuploidy in the crop? 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2022 Abstract Trisomic cauliflower plants (Brassica oleracea L. var. botrytis) display abnormal curd phenotypes that seriously decrease commercial value of the crop. Despite extensive breeding efforts, selection of genotypes producing euploid gametes remains unsuccessful due to unknown genetic and environmental factors. To reveal an eventual role of an-euploid gametes, we analyzed chromosome pairing, chiasma formation and chromosome segregation in pollen mother cells of selected cauliflower genotypes. To this end we compared three genotypes exhibiting Low with < 5%, Moderate with 5–10% and High with > 10% aberrant offspring, respectively. Although chromosome pairing at pachytene was regular, cells at diakinesis and metaphase I showed variable numbers of univalents, suggesting partial desynapsis. Cells at anaphase I–telophase II exhibit various degrees of unbalanced chromosome numbers, that may explain the aneuploid offspring. Immunofluorescence probed with an MLH1 antibody demonstrated fluorescent foci in all genotypes, but their lower numbers do not correspond to the number of putative chiasmata. Interchromosomal connections between chromosomes and bivalents are common at diakinesis and metaphase I, and they contain centromeric and 45S rDNA tandem repeats, but such chromatin connections seem not to affect proper disjoin of the half bivalents at anaphase I. Moreover, male meiosis in the Arabidopsis APETALA1/CAULIFLOWER double mutant with the typical cauliflower phenotype does show interchromosomal connections, but there are no indications for partial desynapsis. The causality of the curd development on the desynapsis in cauliflower is still a matter of debate. Cauliflower (dpeaa)DE-He213 Aneuploidy (dpeaa)DE-He213 Desynapsis (dpeaa)DE-He213 Lelivelt, Cilia aut Wijnker, Erik aut de Jong, Hans (orcid)0000-0003-2262-4941 aut Enthalten in Euphytica Dordrecht [u.a.] : Springer Science + Business Media B.V., 1952 218(2022), 6 vom: 24. Mai (DE-627)312840098 (DE-600)2012322-X 1573-5060 nnns volume:218 year:2022 number:6 day:24 month:05 https://dx.doi.org/10.1007/s10681-022-03027-7 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_211 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 218 2022 6 24 05 |
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10.1007/s10681-022-03027-7 doi (DE-627)SPR047091169 (SPR)s10681-022-03027-7-e DE-627 ger DE-627 rakwb eng Ji, Xianwen verfasserin aut Is partial desynapsis in cauliflower (Brassica oleracea L. var. botrytis) pollen mother cells linked to aneuploidy in the crop? 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2022 Abstract Trisomic cauliflower plants (Brassica oleracea L. var. botrytis) display abnormal curd phenotypes that seriously decrease commercial value of the crop. Despite extensive breeding efforts, selection of genotypes producing euploid gametes remains unsuccessful due to unknown genetic and environmental factors. To reveal an eventual role of an-euploid gametes, we analyzed chromosome pairing, chiasma formation and chromosome segregation in pollen mother cells of selected cauliflower genotypes. To this end we compared three genotypes exhibiting Low with < 5%, Moderate with 5–10% and High with > 10% aberrant offspring, respectively. Although chromosome pairing at pachytene was regular, cells at diakinesis and metaphase I showed variable numbers of univalents, suggesting partial desynapsis. Cells at anaphase I–telophase II exhibit various degrees of unbalanced chromosome numbers, that may explain the aneuploid offspring. Immunofluorescence probed with an MLH1 antibody demonstrated fluorescent foci in all genotypes, but their lower numbers do not correspond to the number of putative chiasmata. Interchromosomal connections between chromosomes and bivalents are common at diakinesis and metaphase I, and they contain centromeric and 45S rDNA tandem repeats, but such chromatin connections seem not to affect proper disjoin of the half bivalents at anaphase I. Moreover, male meiosis in the Arabidopsis APETALA1/CAULIFLOWER double mutant with the typical cauliflower phenotype does show interchromosomal connections, but there are no indications for partial desynapsis. The causality of the curd development on the desynapsis in cauliflower is still a matter of debate. Cauliflower (dpeaa)DE-He213 Aneuploidy (dpeaa)DE-He213 Desynapsis (dpeaa)DE-He213 Lelivelt, Cilia aut Wijnker, Erik aut de Jong, Hans (orcid)0000-0003-2262-4941 aut Enthalten in Euphytica Dordrecht [u.a.] : Springer Science + Business Media B.V., 1952 218(2022), 6 vom: 24. Mai (DE-627)312840098 (DE-600)2012322-X 1573-5060 nnns volume:218 year:2022 number:6 day:24 month:05 https://dx.doi.org/10.1007/s10681-022-03027-7 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_211 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 218 2022 6 24 05 |
allfieldsSound |
10.1007/s10681-022-03027-7 doi (DE-627)SPR047091169 (SPR)s10681-022-03027-7-e DE-627 ger DE-627 rakwb eng Ji, Xianwen verfasserin aut Is partial desynapsis in cauliflower (Brassica oleracea L. var. botrytis) pollen mother cells linked to aneuploidy in the crop? 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2022 Abstract Trisomic cauliflower plants (Brassica oleracea L. var. botrytis) display abnormal curd phenotypes that seriously decrease commercial value of the crop. Despite extensive breeding efforts, selection of genotypes producing euploid gametes remains unsuccessful due to unknown genetic and environmental factors. To reveal an eventual role of an-euploid gametes, we analyzed chromosome pairing, chiasma formation and chromosome segregation in pollen mother cells of selected cauliflower genotypes. To this end we compared three genotypes exhibiting Low with < 5%, Moderate with 5–10% and High with > 10% aberrant offspring, respectively. Although chromosome pairing at pachytene was regular, cells at diakinesis and metaphase I showed variable numbers of univalents, suggesting partial desynapsis. Cells at anaphase I–telophase II exhibit various degrees of unbalanced chromosome numbers, that may explain the aneuploid offspring. Immunofluorescence probed with an MLH1 antibody demonstrated fluorescent foci in all genotypes, but their lower numbers do not correspond to the number of putative chiasmata. Interchromosomal connections between chromosomes and bivalents are common at diakinesis and metaphase I, and they contain centromeric and 45S rDNA tandem repeats, but such chromatin connections seem not to affect proper disjoin of the half bivalents at anaphase I. Moreover, male meiosis in the Arabidopsis APETALA1/CAULIFLOWER double mutant with the typical cauliflower phenotype does show interchromosomal connections, but there are no indications for partial desynapsis. The causality of the curd development on the desynapsis in cauliflower is still a matter of debate. Cauliflower (dpeaa)DE-He213 Aneuploidy (dpeaa)DE-He213 Desynapsis (dpeaa)DE-He213 Lelivelt, Cilia aut Wijnker, Erik aut de Jong, Hans (orcid)0000-0003-2262-4941 aut Enthalten in Euphytica Dordrecht [u.a.] : Springer Science + Business Media B.V., 1952 218(2022), 6 vom: 24. Mai (DE-627)312840098 (DE-600)2012322-X 1573-5060 nnns volume:218 year:2022 number:6 day:24 month:05 https://dx.doi.org/10.1007/s10681-022-03027-7 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_211 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 218 2022 6 24 05 |
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Enthalten in Euphytica 218(2022), 6 vom: 24. Mai volume:218 year:2022 number:6 day:24 month:05 |
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Ji, Xianwen @@aut@@ Lelivelt, Cilia @@aut@@ Wijnker, Erik @@aut@@ de Jong, Hans @@aut@@ |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">SPR047091169</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230507200241.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">220525s2022 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s10681-022-03027-7</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR047091169</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)s10681-022-03027-7-e</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Ji, Xianwen</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Is partial desynapsis in cauliflower (Brassica oleracea L. var. botrytis) pollen mother cells linked to aneuploidy in the crop?</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2022</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© The Author(s) 2022</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Trisomic cauliflower plants (Brassica oleracea L. var. botrytis) display abnormal curd phenotypes that seriously decrease commercial value of the crop. Despite extensive breeding efforts, selection of genotypes producing euploid gametes remains unsuccessful due to unknown genetic and environmental factors. To reveal an eventual role of an-euploid gametes, we analyzed chromosome pairing, chiasma formation and chromosome segregation in pollen mother cells of selected cauliflower genotypes. To this end we compared three genotypes exhibiting Low with < 5%, Moderate with 5–10% and High with > 10% aberrant offspring, respectively. Although chromosome pairing at pachytene was regular, cells at diakinesis and metaphase I showed variable numbers of univalents, suggesting partial desynapsis. Cells at anaphase I–telophase II exhibit various degrees of unbalanced chromosome numbers, that may explain the aneuploid offspring. Immunofluorescence probed with an MLH1 antibody demonstrated fluorescent foci in all genotypes, but their lower numbers do not correspond to the number of putative chiasmata. Interchromosomal connections between chromosomes and bivalents are common at diakinesis and metaphase I, and they contain centromeric and 45S rDNA tandem repeats, but such chromatin connections seem not to affect proper disjoin of the half bivalents at anaphase I. Moreover, male meiosis in the Arabidopsis APETALA1/CAULIFLOWER double mutant with the typical cauliflower phenotype does show interchromosomal connections, but there are no indications for partial desynapsis. 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Ji, Xianwen |
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Ji, Xianwen misc Cauliflower misc Aneuploidy misc Desynapsis Is partial desynapsis in cauliflower (Brassica oleracea L. var. botrytis) pollen mother cells linked to aneuploidy in the crop? |
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Is partial desynapsis in cauliflower (Brassica oleracea L. var. botrytis) pollen mother cells linked to aneuploidy in the crop? Cauliflower (dpeaa)DE-He213 Aneuploidy (dpeaa)DE-He213 Desynapsis (dpeaa)DE-He213 |
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Is partial desynapsis in cauliflower (Brassica oleracea L. var. botrytis) pollen mother cells linked to aneuploidy in the crop? |
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Is partial desynapsis in cauliflower (Brassica oleracea L. var. botrytis) pollen mother cells linked to aneuploidy in the crop? |
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Ji, Xianwen Lelivelt, Cilia Wijnker, Erik de Jong, Hans |
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is partial desynapsis in cauliflower (brassica oleracea l. var. botrytis) pollen mother cells linked to aneuploidy in the crop? |
title_auth |
Is partial desynapsis in cauliflower (Brassica oleracea L. var. botrytis) pollen mother cells linked to aneuploidy in the crop? |
abstract |
Abstract Trisomic cauliflower plants (Brassica oleracea L. var. botrytis) display abnormal curd phenotypes that seriously decrease commercial value of the crop. Despite extensive breeding efforts, selection of genotypes producing euploid gametes remains unsuccessful due to unknown genetic and environmental factors. To reveal an eventual role of an-euploid gametes, we analyzed chromosome pairing, chiasma formation and chromosome segregation in pollen mother cells of selected cauliflower genotypes. To this end we compared three genotypes exhibiting Low with < 5%, Moderate with 5–10% and High with > 10% aberrant offspring, respectively. Although chromosome pairing at pachytene was regular, cells at diakinesis and metaphase I showed variable numbers of univalents, suggesting partial desynapsis. Cells at anaphase I–telophase II exhibit various degrees of unbalanced chromosome numbers, that may explain the aneuploid offspring. Immunofluorescence probed with an MLH1 antibody demonstrated fluorescent foci in all genotypes, but their lower numbers do not correspond to the number of putative chiasmata. Interchromosomal connections between chromosomes and bivalents are common at diakinesis and metaphase I, and they contain centromeric and 45S rDNA tandem repeats, but such chromatin connections seem not to affect proper disjoin of the half bivalents at anaphase I. Moreover, male meiosis in the Arabidopsis APETALA1/CAULIFLOWER double mutant with the typical cauliflower phenotype does show interchromosomal connections, but there are no indications for partial desynapsis. The causality of the curd development on the desynapsis in cauliflower is still a matter of debate. © The Author(s) 2022 |
abstractGer |
Abstract Trisomic cauliflower plants (Brassica oleracea L. var. botrytis) display abnormal curd phenotypes that seriously decrease commercial value of the crop. Despite extensive breeding efforts, selection of genotypes producing euploid gametes remains unsuccessful due to unknown genetic and environmental factors. To reveal an eventual role of an-euploid gametes, we analyzed chromosome pairing, chiasma formation and chromosome segregation in pollen mother cells of selected cauliflower genotypes. To this end we compared three genotypes exhibiting Low with < 5%, Moderate with 5–10% and High with > 10% aberrant offspring, respectively. Although chromosome pairing at pachytene was regular, cells at diakinesis and metaphase I showed variable numbers of univalents, suggesting partial desynapsis. Cells at anaphase I–telophase II exhibit various degrees of unbalanced chromosome numbers, that may explain the aneuploid offspring. Immunofluorescence probed with an MLH1 antibody demonstrated fluorescent foci in all genotypes, but their lower numbers do not correspond to the number of putative chiasmata. Interchromosomal connections between chromosomes and bivalents are common at diakinesis and metaphase I, and they contain centromeric and 45S rDNA tandem repeats, but such chromatin connections seem not to affect proper disjoin of the half bivalents at anaphase I. Moreover, male meiosis in the Arabidopsis APETALA1/CAULIFLOWER double mutant with the typical cauliflower phenotype does show interchromosomal connections, but there are no indications for partial desynapsis. The causality of the curd development on the desynapsis in cauliflower is still a matter of debate. © The Author(s) 2022 |
abstract_unstemmed |
Abstract Trisomic cauliflower plants (Brassica oleracea L. var. botrytis) display abnormal curd phenotypes that seriously decrease commercial value of the crop. Despite extensive breeding efforts, selection of genotypes producing euploid gametes remains unsuccessful due to unknown genetic and environmental factors. To reveal an eventual role of an-euploid gametes, we analyzed chromosome pairing, chiasma formation and chromosome segregation in pollen mother cells of selected cauliflower genotypes. To this end we compared three genotypes exhibiting Low with < 5%, Moderate with 5–10% and High with > 10% aberrant offspring, respectively. Although chromosome pairing at pachytene was regular, cells at diakinesis and metaphase I showed variable numbers of univalents, suggesting partial desynapsis. Cells at anaphase I–telophase II exhibit various degrees of unbalanced chromosome numbers, that may explain the aneuploid offspring. Immunofluorescence probed with an MLH1 antibody demonstrated fluorescent foci in all genotypes, but their lower numbers do not correspond to the number of putative chiasmata. Interchromosomal connections between chromosomes and bivalents are common at diakinesis and metaphase I, and they contain centromeric and 45S rDNA tandem repeats, but such chromatin connections seem not to affect proper disjoin of the half bivalents at anaphase I. Moreover, male meiosis in the Arabidopsis APETALA1/CAULIFLOWER double mutant with the typical cauliflower phenotype does show interchromosomal connections, but there are no indications for partial desynapsis. The causality of the curd development on the desynapsis in cauliflower is still a matter of debate. © The Author(s) 2022 |
collection_details |
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container_issue |
6 |
title_short |
Is partial desynapsis in cauliflower (Brassica oleracea L. var. botrytis) pollen mother cells linked to aneuploidy in the crop? |
url |
https://dx.doi.org/10.1007/s10681-022-03027-7 |
remote_bool |
true |
author2 |
Lelivelt, Cilia Wijnker, Erik de Jong, Hans |
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Lelivelt, Cilia Wijnker, Erik de Jong, Hans |
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doi_str |
10.1007/s10681-022-03027-7 |
up_date |
2024-07-04T01:49:24.906Z |
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|
score |
7.399207 |