Genetic diversity and population genetic structure analysis of Apis mellifera subspecies in Algeria and Europe based on complementary sex determiner (CSD) gene
Abstract In honeybees, the mechanism of sex determination depends on genetic variation at the complementary sex determiner (CSD) locus, which has a large allelic diversity. In this study, we examined the population genetic structure and genetic diversity within the highly variable region (HVR) of CS...
Ausführliche Beschreibung
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| Autor*in: |
FRIDI, Riad [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: Apidologie - Paris : Springer, 1970, 53(2022), 1 vom: März |
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| Übergeordnetes Werk: |
volume:53 ; year:2022 ; number:1 ; month:03 |
| Links: |
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| DOI / URN: |
10.1007/s13592-022-00920-x |
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| Katalog-ID: |
SPR046416501 |
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| 100 | 1 | |a FRIDI, Riad |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Genetic diversity and population genetic structure analysis of Apis mellifera subspecies in Algeria and Europe based on complementary sex determiner (CSD) gene |
| 264 | 1 | |c 2022 | |
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| 520 | |a Abstract In honeybees, the mechanism of sex determination depends on genetic variation at the complementary sex determiner (CSD) locus, which has a large allelic diversity. In this study, we examined the population genetic structure and genetic diversity within the highly variable region (HVR) of CSD in five Apis mellifera subspecies, in addition to Buckfast and unknown mixed ancestry bees. We sequenced CSD in 329 drones, 146 from Algeria (A. m. intermissa and A. m. sahariensis subspecies) and 183 from Europe (A. m. ligustica, A. m. carnica, A. m. mellifera subspecies, Buckfast samples, and individuals of unknown mixed ancestry). A total of 119 nucleotide haplotypes were detected. These corresponded to 119 protein haplotypes, of which 81 were new. The analysis of these haplotypes showed that HVR diversity levels were comparable with those in other populations of honeybee worldwide. Paradoxically, this high level of diversity at the locus did not allow for a separation of the samples according to their subspecies origin, which suggested either an evolutionary convergence or a conservation of alleles across subspecies, and an absence of genetic drift. Our results can be used to provide more information about the CSD diversity to include in breeding programs of honeybee populations. | ||
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10.1007/s13592-022-00920-x doi (DE-627)SPR046416501 (SPR)s13592-022-00920-x-e DE-627 ger DE-627 rakwb eng FRIDI, Riad verfasserin aut Genetic diversity and population genetic structure analysis of Apis mellifera subspecies in Algeria and Europe based on complementary sex determiner (CSD) gene 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2022 Abstract In honeybees, the mechanism of sex determination depends on genetic variation at the complementary sex determiner (CSD) locus, which has a large allelic diversity. In this study, we examined the population genetic structure and genetic diversity within the highly variable region (HVR) of CSD in five Apis mellifera subspecies, in addition to Buckfast and unknown mixed ancestry bees. We sequenced CSD in 329 drones, 146 from Algeria (A. m. intermissa and A. m. sahariensis subspecies) and 183 from Europe (A. m. ligustica, A. m. carnica, A. m. mellifera subspecies, Buckfast samples, and individuals of unknown mixed ancestry). A total of 119 nucleotide haplotypes were detected. These corresponded to 119 protein haplotypes, of which 81 were new. The analysis of these haplotypes showed that HVR diversity levels were comparable with those in other populations of honeybee worldwide. Paradoxically, this high level of diversity at the locus did not allow for a separation of the samples according to their subspecies origin, which suggested either an evolutionary convergence or a conservation of alleles across subspecies, and an absence of genetic drift. Our results can be used to provide more information about the CSD diversity to include in breeding programs of honeybee populations. complementary sex determiner (dpeaa)DE-He213 polymorphism (dpeaa)DE-He213 genetic diversity (dpeaa)DE-He213 TABET AOUL, Nacera (orcid)0000-0003-0683-0139 aut CATAYS, Guillaume aut BASSO, Benjamin aut BIENEFELD, Kaspar (orcid)0000-0002-5201-475X aut GREGORC, Aleš (orcid)0000-0001-7988-6796 aut VIGNAL, Alain (orcid)0000-0002-6797-2125 aut CANALE-TABET, Kamila aut Enthalten in Apidologie Paris : Springer, 1970 53(2022), 1 vom: März (DE-627)312842996 (DE-600)2005148-7 1297-9678 nnns volume:53 year:2022 number:1 month:03 https://dx.doi.org/10.1007/s13592-022-00920-x 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_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_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_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 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_4367 GBV_ILN_4393 GBV_ILN_4700 AR 53 2022 1 03 |
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10.1007/s13592-022-00920-x doi (DE-627)SPR046416501 (SPR)s13592-022-00920-x-e DE-627 ger DE-627 rakwb eng FRIDI, Riad verfasserin aut Genetic diversity and population genetic structure analysis of Apis mellifera subspecies in Algeria and Europe based on complementary sex determiner (CSD) gene 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2022 Abstract In honeybees, the mechanism of sex determination depends on genetic variation at the complementary sex determiner (CSD) locus, which has a large allelic diversity. In this study, we examined the population genetic structure and genetic diversity within the highly variable region (HVR) of CSD in five Apis mellifera subspecies, in addition to Buckfast and unknown mixed ancestry bees. We sequenced CSD in 329 drones, 146 from Algeria (A. m. intermissa and A. m. sahariensis subspecies) and 183 from Europe (A. m. ligustica, A. m. carnica, A. m. mellifera subspecies, Buckfast samples, and individuals of unknown mixed ancestry). A total of 119 nucleotide haplotypes were detected. These corresponded to 119 protein haplotypes, of which 81 were new. The analysis of these haplotypes showed that HVR diversity levels were comparable with those in other populations of honeybee worldwide. Paradoxically, this high level of diversity at the locus did not allow for a separation of the samples according to their subspecies origin, which suggested either an evolutionary convergence or a conservation of alleles across subspecies, and an absence of genetic drift. Our results can be used to provide more information about the CSD diversity to include in breeding programs of honeybee populations. complementary sex determiner (dpeaa)DE-He213 polymorphism (dpeaa)DE-He213 genetic diversity (dpeaa)DE-He213 TABET AOUL, Nacera (orcid)0000-0003-0683-0139 aut CATAYS, Guillaume aut BASSO, Benjamin aut BIENEFELD, Kaspar (orcid)0000-0002-5201-475X aut GREGORC, Aleš (orcid)0000-0001-7988-6796 aut VIGNAL, Alain (orcid)0000-0002-6797-2125 aut CANALE-TABET, Kamila aut Enthalten in Apidologie Paris : Springer, 1970 53(2022), 1 vom: März (DE-627)312842996 (DE-600)2005148-7 1297-9678 nnns volume:53 year:2022 number:1 month:03 https://dx.doi.org/10.1007/s13592-022-00920-x 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_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_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_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 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_4367 GBV_ILN_4393 GBV_ILN_4700 AR 53 2022 1 03 |
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10.1007/s13592-022-00920-x doi (DE-627)SPR046416501 (SPR)s13592-022-00920-x-e DE-627 ger DE-627 rakwb eng FRIDI, Riad verfasserin aut Genetic diversity and population genetic structure analysis of Apis mellifera subspecies in Algeria and Europe based on complementary sex determiner (CSD) gene 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2022 Abstract In honeybees, the mechanism of sex determination depends on genetic variation at the complementary sex determiner (CSD) locus, which has a large allelic diversity. In this study, we examined the population genetic structure and genetic diversity within the highly variable region (HVR) of CSD in five Apis mellifera subspecies, in addition to Buckfast and unknown mixed ancestry bees. We sequenced CSD in 329 drones, 146 from Algeria (A. m. intermissa and A. m. sahariensis subspecies) and 183 from Europe (A. m. ligustica, A. m. carnica, A. m. mellifera subspecies, Buckfast samples, and individuals of unknown mixed ancestry). A total of 119 nucleotide haplotypes were detected. These corresponded to 119 protein haplotypes, of which 81 were new. The analysis of these haplotypes showed that HVR diversity levels were comparable with those in other populations of honeybee worldwide. Paradoxically, this high level of diversity at the locus did not allow for a separation of the samples according to their subspecies origin, which suggested either an evolutionary convergence or a conservation of alleles across subspecies, and an absence of genetic drift. Our results can be used to provide more information about the CSD diversity to include in breeding programs of honeybee populations. complementary sex determiner (dpeaa)DE-He213 polymorphism (dpeaa)DE-He213 genetic diversity (dpeaa)DE-He213 TABET AOUL, Nacera (orcid)0000-0003-0683-0139 aut CATAYS, Guillaume aut BASSO, Benjamin aut BIENEFELD, Kaspar (orcid)0000-0002-5201-475X aut GREGORC, Aleš (orcid)0000-0001-7988-6796 aut VIGNAL, Alain (orcid)0000-0002-6797-2125 aut CANALE-TABET, Kamila aut Enthalten in Apidologie Paris : Springer, 1970 53(2022), 1 vom: März (DE-627)312842996 (DE-600)2005148-7 1297-9678 nnns volume:53 year:2022 number:1 month:03 https://dx.doi.org/10.1007/s13592-022-00920-x 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_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_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_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 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_4367 GBV_ILN_4393 GBV_ILN_4700 AR 53 2022 1 03 |
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10.1007/s13592-022-00920-x doi (DE-627)SPR046416501 (SPR)s13592-022-00920-x-e DE-627 ger DE-627 rakwb eng FRIDI, Riad verfasserin aut Genetic diversity and population genetic structure analysis of Apis mellifera subspecies in Algeria and Europe based on complementary sex determiner (CSD) gene 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2022 Abstract In honeybees, the mechanism of sex determination depends on genetic variation at the complementary sex determiner (CSD) locus, which has a large allelic diversity. In this study, we examined the population genetic structure and genetic diversity within the highly variable region (HVR) of CSD in five Apis mellifera subspecies, in addition to Buckfast and unknown mixed ancestry bees. We sequenced CSD in 329 drones, 146 from Algeria (A. m. intermissa and A. m. sahariensis subspecies) and 183 from Europe (A. m. ligustica, A. m. carnica, A. m. mellifera subspecies, Buckfast samples, and individuals of unknown mixed ancestry). A total of 119 nucleotide haplotypes were detected. These corresponded to 119 protein haplotypes, of which 81 were new. The analysis of these haplotypes showed that HVR diversity levels were comparable with those in other populations of honeybee worldwide. Paradoxically, this high level of diversity at the locus did not allow for a separation of the samples according to their subspecies origin, which suggested either an evolutionary convergence or a conservation of alleles across subspecies, and an absence of genetic drift. Our results can be used to provide more information about the CSD diversity to include in breeding programs of honeybee populations. complementary sex determiner (dpeaa)DE-He213 polymorphism (dpeaa)DE-He213 genetic diversity (dpeaa)DE-He213 TABET AOUL, Nacera (orcid)0000-0003-0683-0139 aut CATAYS, Guillaume aut BASSO, Benjamin aut BIENEFELD, Kaspar (orcid)0000-0002-5201-475X aut GREGORC, Aleš (orcid)0000-0001-7988-6796 aut VIGNAL, Alain (orcid)0000-0002-6797-2125 aut CANALE-TABET, Kamila aut Enthalten in Apidologie Paris : Springer, 1970 53(2022), 1 vom: März (DE-627)312842996 (DE-600)2005148-7 1297-9678 nnns volume:53 year:2022 number:1 month:03 https://dx.doi.org/10.1007/s13592-022-00920-x 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_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_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_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 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_4367 GBV_ILN_4393 GBV_ILN_4700 AR 53 2022 1 03 |
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10.1007/s13592-022-00920-x doi (DE-627)SPR046416501 (SPR)s13592-022-00920-x-e DE-627 ger DE-627 rakwb eng FRIDI, Riad verfasserin aut Genetic diversity and population genetic structure analysis of Apis mellifera subspecies in Algeria and Europe based on complementary sex determiner (CSD) gene 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2022 Abstract In honeybees, the mechanism of sex determination depends on genetic variation at the complementary sex determiner (CSD) locus, which has a large allelic diversity. In this study, we examined the population genetic structure and genetic diversity within the highly variable region (HVR) of CSD in five Apis mellifera subspecies, in addition to Buckfast and unknown mixed ancestry bees. We sequenced CSD in 329 drones, 146 from Algeria (A. m. intermissa and A. m. sahariensis subspecies) and 183 from Europe (A. m. ligustica, A. m. carnica, A. m. mellifera subspecies, Buckfast samples, and individuals of unknown mixed ancestry). A total of 119 nucleotide haplotypes were detected. These corresponded to 119 protein haplotypes, of which 81 were new. The analysis of these haplotypes showed that HVR diversity levels were comparable with those in other populations of honeybee worldwide. Paradoxically, this high level of diversity at the locus did not allow for a separation of the samples according to their subspecies origin, which suggested either an evolutionary convergence or a conservation of alleles across subspecies, and an absence of genetic drift. Our results can be used to provide more information about the CSD diversity to include in breeding programs of honeybee populations. complementary sex determiner (dpeaa)DE-He213 polymorphism (dpeaa)DE-He213 genetic diversity (dpeaa)DE-He213 TABET AOUL, Nacera (orcid)0000-0003-0683-0139 aut CATAYS, Guillaume aut BASSO, Benjamin aut BIENEFELD, Kaspar (orcid)0000-0002-5201-475X aut GREGORC, Aleš (orcid)0000-0001-7988-6796 aut VIGNAL, Alain (orcid)0000-0002-6797-2125 aut CANALE-TABET, Kamila aut Enthalten in Apidologie Paris : Springer, 1970 53(2022), 1 vom: März (DE-627)312842996 (DE-600)2005148-7 1297-9678 nnns volume:53 year:2022 number:1 month:03 https://dx.doi.org/10.1007/s13592-022-00920-x 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_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_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_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 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_4367 GBV_ILN_4393 GBV_ILN_4700 AR 53 2022 1 03 |
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Enthalten in Apidologie 53(2022), 1 vom: März volume:53 year:2022 number:1 month:03 |
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FRIDI, Riad @@aut@@ TABET AOUL, Nacera @@aut@@ CATAYS, Guillaume @@aut@@ BASSO, Benjamin @@aut@@ BIENEFELD, Kaspar @@aut@@ GREGORC, Aleš @@aut@@ VIGNAL, Alain @@aut@@ CANALE-TABET, Kamila @@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">SPR046416501</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230507171720.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">220308s2022 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s13592-022-00920-x</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR046416501</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)s13592-022-00920-x-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">FRIDI, Riad</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Genetic diversity and population genetic structure analysis of Apis mellifera subspecies in Algeria and Europe based on complementary sex determiner (CSD) gene</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 In honeybees, the mechanism of sex determination depends on genetic variation at the complementary sex determiner (CSD) locus, which has a large allelic diversity. In this study, we examined the population genetic structure and genetic diversity within the highly variable region (HVR) of CSD in five Apis mellifera subspecies, in addition to Buckfast and unknown mixed ancestry bees. We sequenced CSD in 329 drones, 146 from Algeria (A. m. intermissa and A. m. sahariensis subspecies) and 183 from Europe (A. m. ligustica, A. m. carnica, A. m. mellifera subspecies, Buckfast samples, and individuals of unknown mixed ancestry). A total of 119 nucleotide haplotypes were detected. These corresponded to 119 protein haplotypes, of which 81 were new. The analysis of these haplotypes showed that HVR diversity levels were comparable with those in other populations of honeybee worldwide. Paradoxically, this high level of diversity at the locus did not allow for a separation of the samples according to their subspecies origin, which suggested either an evolutionary convergence or a conservation of alleles across subspecies, and an absence of genetic drift. 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FRIDI, Riad misc complementary sex determiner misc polymorphism misc genetic diversity Genetic diversity and population genetic structure analysis of Apis mellifera subspecies in Algeria and Europe based on complementary sex determiner (CSD) gene |
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Genetic diversity and population genetic structure analysis of Apis mellifera subspecies in Algeria and Europe based on complementary sex determiner (CSD) gene complementary sex determiner (dpeaa)DE-He213 polymorphism (dpeaa)DE-He213 genetic diversity (dpeaa)DE-He213 |
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Genetic diversity and population genetic structure analysis of Apis mellifera subspecies in Algeria and Europe based on complementary sex determiner (CSD) gene |
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Genetic diversity and population genetic structure analysis of Apis mellifera subspecies in Algeria and Europe based on complementary sex determiner (CSD) gene |
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FRIDI, Riad TABET AOUL, Nacera CATAYS, Guillaume BASSO, Benjamin BIENEFELD, Kaspar GREGORC, Aleš VIGNAL, Alain CANALE-TABET, Kamila |
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genetic diversity and population genetic structure analysis of apis mellifera subspecies in algeria and europe based on complementary sex determiner (csd) gene |
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Genetic diversity and population genetic structure analysis of Apis mellifera subspecies in Algeria and Europe based on complementary sex determiner (CSD) gene |
| abstract |
Abstract In honeybees, the mechanism of sex determination depends on genetic variation at the complementary sex determiner (CSD) locus, which has a large allelic diversity. In this study, we examined the population genetic structure and genetic diversity within the highly variable region (HVR) of CSD in five Apis mellifera subspecies, in addition to Buckfast and unknown mixed ancestry bees. We sequenced CSD in 329 drones, 146 from Algeria (A. m. intermissa and A. m. sahariensis subspecies) and 183 from Europe (A. m. ligustica, A. m. carnica, A. m. mellifera subspecies, Buckfast samples, and individuals of unknown mixed ancestry). A total of 119 nucleotide haplotypes were detected. These corresponded to 119 protein haplotypes, of which 81 were new. The analysis of these haplotypes showed that HVR diversity levels were comparable with those in other populations of honeybee worldwide. Paradoxically, this high level of diversity at the locus did not allow for a separation of the samples according to their subspecies origin, which suggested either an evolutionary convergence or a conservation of alleles across subspecies, and an absence of genetic drift. Our results can be used to provide more information about the CSD diversity to include in breeding programs of honeybee populations. © The Author(s) 2022 |
| abstractGer |
Abstract In honeybees, the mechanism of sex determination depends on genetic variation at the complementary sex determiner (CSD) locus, which has a large allelic diversity. In this study, we examined the population genetic structure and genetic diversity within the highly variable region (HVR) of CSD in five Apis mellifera subspecies, in addition to Buckfast and unknown mixed ancestry bees. We sequenced CSD in 329 drones, 146 from Algeria (A. m. intermissa and A. m. sahariensis subspecies) and 183 from Europe (A. m. ligustica, A. m. carnica, A. m. mellifera subspecies, Buckfast samples, and individuals of unknown mixed ancestry). A total of 119 nucleotide haplotypes were detected. These corresponded to 119 protein haplotypes, of which 81 were new. The analysis of these haplotypes showed that HVR diversity levels were comparable with those in other populations of honeybee worldwide. Paradoxically, this high level of diversity at the locus did not allow for a separation of the samples according to their subspecies origin, which suggested either an evolutionary convergence or a conservation of alleles across subspecies, and an absence of genetic drift. Our results can be used to provide more information about the CSD diversity to include in breeding programs of honeybee populations. © The Author(s) 2022 |
| abstract_unstemmed |
Abstract In honeybees, the mechanism of sex determination depends on genetic variation at the complementary sex determiner (CSD) locus, which has a large allelic diversity. In this study, we examined the population genetic structure and genetic diversity within the highly variable region (HVR) of CSD in five Apis mellifera subspecies, in addition to Buckfast and unknown mixed ancestry bees. We sequenced CSD in 329 drones, 146 from Algeria (A. m. intermissa and A. m. sahariensis subspecies) and 183 from Europe (A. m. ligustica, A. m. carnica, A. m. mellifera subspecies, Buckfast samples, and individuals of unknown mixed ancestry). A total of 119 nucleotide haplotypes were detected. These corresponded to 119 protein haplotypes, of which 81 were new. The analysis of these haplotypes showed that HVR diversity levels were comparable with those in other populations of honeybee worldwide. Paradoxically, this high level of diversity at the locus did not allow for a separation of the samples according to their subspecies origin, which suggested either an evolutionary convergence or a conservation of alleles across subspecies, and an absence of genetic drift. Our results can be used to provide more information about the CSD diversity to include in breeding programs of honeybee populations. © The Author(s) 2022 |
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| title_short |
Genetic diversity and population genetic structure analysis of Apis mellifera subspecies in Algeria and Europe based on complementary sex determiner (CSD) gene |
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https://dx.doi.org/10.1007/s13592-022-00920-x |
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TABET AOUL, Nacera CATAYS, Guillaume BASSO, Benjamin BIENEFELD, Kaspar GREGORC, Aleš VIGNAL, Alain CANALE-TABET, Kamila |
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TABET AOUL, Nacera CATAYS, Guillaume BASSO, Benjamin BIENEFELD, Kaspar GREGORC, Aleš VIGNAL, Alain CANALE-TABET, Kamila |
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10.1007/s13592-022-00920-x |
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| score |
7.4000263 |