Extraordinary chromosome diversity in the southernmost populations of the montane grass mouse Akodon montensis (Cricetidae, Sigmodontinae)
Abstract Akodon montensis is abundant and widely distributed in the Atlantic Forest, which southern limits extends to northern Argentina, principally in the Misiones province. Chromosomal data from more centrally distributed populations in Brazil showed significant chromosome diversity; however, dat...
Ausführliche Beschreibung
Autor*in: |
Labaroni, Carolina A. [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2023 |
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Anmerkung: |
© The Author(s), under exclusive licence to Mammal Research Institute Polish Academy of Sciences 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
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Übergeordnetes Werk: |
Enthalten in: Mammal research - Heidelberg : Springer, 2015, 68(2023), 3 vom: 13. Apr., Seite 355-365 |
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Übergeordnetes Werk: |
volume:68 ; year:2023 ; number:3 ; day:13 ; month:04 ; pages:355-365 |
Links: |
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DOI / URN: |
10.1007/s13364-023-00687-1 |
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Katalog-ID: |
SPR051849461 |
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520 | |a Abstract Akodon montensis is abundant and widely distributed in the Atlantic Forest, which southern limits extends to northern Argentina, principally in the Misiones province. Chromosomal data from more centrally distributed populations in Brazil showed significant chromosome diversity; however, data from its southern boundaries are scarce. To explore the chromosomal diversity of this species, we conducted conventional chromosome staining, C-banding, $ CMA_{3} $/DAPI fluorochromes, and in situ hybridization with a telomere probe in samples from Argentina. Most specimens had the standard karyotype 2n = 24, although numerical variations due to aneuploidies and supernumerary (B) chromosomes were detected. We registered novel structural polymorphisms for pair 11 and sex chromosomes, and a rearrangement involving pairs 2 and 4, possibly due to a spontaneous chromosomal mutation. Most A. montensis females are homogametic with XX sex chromosomes, although XY and X0 females were observed. Most individuals carrying B chromosomes had 1 B and, to a lesser extent, 2 and 3 B. The chromosomal variability detected at the southern limit of A. montensis distribution is high and similar to other geographically distant populations, despite the fact that it could be a region recently colonized. Some of these variations are unique and could have originated independently in southern populations, while others are shared throughout the species distribution and may have originated earlier. | ||
650 | 4 | |a Aneuploidy |7 (dpeaa)DE-He213 | |
650 | 4 | |a chromosomal rearrangement |7 (dpeaa)DE-He213 | |
650 | 4 | |a sex-chromosomes polymorphism |7 (dpeaa)DE-He213 | |
650 | 4 | |a supernumerary chromosomes |7 (dpeaa)DE-He213 | |
650 | 4 | |a evolution |7 (dpeaa)DE-He213 | |
650 | 4 | |a rodent |7 (dpeaa)DE-He213 | |
700 | 1 | |a Ferro, Juan M. |4 aut | |
700 | 1 | |a Buschiazzo, Leandro |4 aut | |
700 | 1 | |a De Cena, Romina |4 aut | |
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700 | 1 | |a Calcena, Eugenio |4 aut | |
700 | 1 | |a Bolzan, Alejandro |4 aut | |
700 | 1 | |a Lanzone, Cecilia |4 aut | |
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10.1007/s13364-023-00687-1 doi (DE-627)SPR051849461 (SPR)s13364-023-00687-1-e DE-627 ger DE-627 rakwb eng Labaroni, Carolina A. verfasserin (orcid)0000-0001-5255-0897 aut Extraordinary chromosome diversity in the southernmost populations of the montane grass mouse Akodon montensis (Cricetidae, Sigmodontinae) 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Mammal Research Institute Polish Academy of Sciences 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract Akodon montensis is abundant and widely distributed in the Atlantic Forest, which southern limits extends to northern Argentina, principally in the Misiones province. Chromosomal data from more centrally distributed populations in Brazil showed significant chromosome diversity; however, data from its southern boundaries are scarce. To explore the chromosomal diversity of this species, we conducted conventional chromosome staining, C-banding, $ CMA_{3} $/DAPI fluorochromes, and in situ hybridization with a telomere probe in samples from Argentina. Most specimens had the standard karyotype 2n = 24, although numerical variations due to aneuploidies and supernumerary (B) chromosomes were detected. We registered novel structural polymorphisms for pair 11 and sex chromosomes, and a rearrangement involving pairs 2 and 4, possibly due to a spontaneous chromosomal mutation. Most A. montensis females are homogametic with XX sex chromosomes, although XY and X0 females were observed. Most individuals carrying B chromosomes had 1 B and, to a lesser extent, 2 and 3 B. The chromosomal variability detected at the southern limit of A. montensis distribution is high and similar to other geographically distant populations, despite the fact that it could be a region recently colonized. Some of these variations are unique and could have originated independently in southern populations, while others are shared throughout the species distribution and may have originated earlier. Aneuploidy (dpeaa)DE-He213 chromosomal rearrangement (dpeaa)DE-He213 sex-chromosomes polymorphism (dpeaa)DE-He213 supernumerary chromosomes (dpeaa)DE-He213 evolution (dpeaa)DE-He213 rodent (dpeaa)DE-He213 Ferro, Juan M. aut Buschiazzo, Leandro aut De Cena, Romina aut Kleiniving, Marcelo aut García, Gabriela aut Calcena, Eugenio aut Bolzan, Alejandro aut Lanzone, Cecilia aut Enthalten in Mammal research Heidelberg : Springer, 2015 68(2023), 3 vom: 13. Apr., Seite 355-365 (DE-627)817359311 (DE-600)2808353-2 2199-241X nnns volume:68 year:2023 number:3 day:13 month:04 pages:355-365 https://dx.doi.org/10.1007/s13364-023-00687-1 lizenzpflichtig 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_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 68 2023 3 13 04 355-365 |
spelling |
10.1007/s13364-023-00687-1 doi (DE-627)SPR051849461 (SPR)s13364-023-00687-1-e DE-627 ger DE-627 rakwb eng Labaroni, Carolina A. verfasserin (orcid)0000-0001-5255-0897 aut Extraordinary chromosome diversity in the southernmost populations of the montane grass mouse Akodon montensis (Cricetidae, Sigmodontinae) 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Mammal Research Institute Polish Academy of Sciences 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract Akodon montensis is abundant and widely distributed in the Atlantic Forest, which southern limits extends to northern Argentina, principally in the Misiones province. Chromosomal data from more centrally distributed populations in Brazil showed significant chromosome diversity; however, data from its southern boundaries are scarce. To explore the chromosomal diversity of this species, we conducted conventional chromosome staining, C-banding, $ CMA_{3} $/DAPI fluorochromes, and in situ hybridization with a telomere probe in samples from Argentina. Most specimens had the standard karyotype 2n = 24, although numerical variations due to aneuploidies and supernumerary (B) chromosomes were detected. We registered novel structural polymorphisms for pair 11 and sex chromosomes, and a rearrangement involving pairs 2 and 4, possibly due to a spontaneous chromosomal mutation. Most A. montensis females are homogametic with XX sex chromosomes, although XY and X0 females were observed. Most individuals carrying B chromosomes had 1 B and, to a lesser extent, 2 and 3 B. The chromosomal variability detected at the southern limit of A. montensis distribution is high and similar to other geographically distant populations, despite the fact that it could be a region recently colonized. Some of these variations are unique and could have originated independently in southern populations, while others are shared throughout the species distribution and may have originated earlier. Aneuploidy (dpeaa)DE-He213 chromosomal rearrangement (dpeaa)DE-He213 sex-chromosomes polymorphism (dpeaa)DE-He213 supernumerary chromosomes (dpeaa)DE-He213 evolution (dpeaa)DE-He213 rodent (dpeaa)DE-He213 Ferro, Juan M. aut Buschiazzo, Leandro aut De Cena, Romina aut Kleiniving, Marcelo aut García, Gabriela aut Calcena, Eugenio aut Bolzan, Alejandro aut Lanzone, Cecilia aut Enthalten in Mammal research Heidelberg : Springer, 2015 68(2023), 3 vom: 13. Apr., Seite 355-365 (DE-627)817359311 (DE-600)2808353-2 2199-241X nnns volume:68 year:2023 number:3 day:13 month:04 pages:355-365 https://dx.doi.org/10.1007/s13364-023-00687-1 lizenzpflichtig 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_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 68 2023 3 13 04 355-365 |
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10.1007/s13364-023-00687-1 doi (DE-627)SPR051849461 (SPR)s13364-023-00687-1-e DE-627 ger DE-627 rakwb eng Labaroni, Carolina A. verfasserin (orcid)0000-0001-5255-0897 aut Extraordinary chromosome diversity in the southernmost populations of the montane grass mouse Akodon montensis (Cricetidae, Sigmodontinae) 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Mammal Research Institute Polish Academy of Sciences 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract Akodon montensis is abundant and widely distributed in the Atlantic Forest, which southern limits extends to northern Argentina, principally in the Misiones province. Chromosomal data from more centrally distributed populations in Brazil showed significant chromosome diversity; however, data from its southern boundaries are scarce. To explore the chromosomal diversity of this species, we conducted conventional chromosome staining, C-banding, $ CMA_{3} $/DAPI fluorochromes, and in situ hybridization with a telomere probe in samples from Argentina. Most specimens had the standard karyotype 2n = 24, although numerical variations due to aneuploidies and supernumerary (B) chromosomes were detected. We registered novel structural polymorphisms for pair 11 and sex chromosomes, and a rearrangement involving pairs 2 and 4, possibly due to a spontaneous chromosomal mutation. Most A. montensis females are homogametic with XX sex chromosomes, although XY and X0 females were observed. Most individuals carrying B chromosomes had 1 B and, to a lesser extent, 2 and 3 B. The chromosomal variability detected at the southern limit of A. montensis distribution is high and similar to other geographically distant populations, despite the fact that it could be a region recently colonized. Some of these variations are unique and could have originated independently in southern populations, while others are shared throughout the species distribution and may have originated earlier. Aneuploidy (dpeaa)DE-He213 chromosomal rearrangement (dpeaa)DE-He213 sex-chromosomes polymorphism (dpeaa)DE-He213 supernumerary chromosomes (dpeaa)DE-He213 evolution (dpeaa)DE-He213 rodent (dpeaa)DE-He213 Ferro, Juan M. aut Buschiazzo, Leandro aut De Cena, Romina aut Kleiniving, Marcelo aut García, Gabriela aut Calcena, Eugenio aut Bolzan, Alejandro aut Lanzone, Cecilia aut Enthalten in Mammal research Heidelberg : Springer, 2015 68(2023), 3 vom: 13. Apr., Seite 355-365 (DE-627)817359311 (DE-600)2808353-2 2199-241X nnns volume:68 year:2023 number:3 day:13 month:04 pages:355-365 https://dx.doi.org/10.1007/s13364-023-00687-1 lizenzpflichtig 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_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 68 2023 3 13 04 355-365 |
allfieldsGer |
10.1007/s13364-023-00687-1 doi (DE-627)SPR051849461 (SPR)s13364-023-00687-1-e DE-627 ger DE-627 rakwb eng Labaroni, Carolina A. verfasserin (orcid)0000-0001-5255-0897 aut Extraordinary chromosome diversity in the southernmost populations of the montane grass mouse Akodon montensis (Cricetidae, Sigmodontinae) 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Mammal Research Institute Polish Academy of Sciences 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract Akodon montensis is abundant and widely distributed in the Atlantic Forest, which southern limits extends to northern Argentina, principally in the Misiones province. Chromosomal data from more centrally distributed populations in Brazil showed significant chromosome diversity; however, data from its southern boundaries are scarce. To explore the chromosomal diversity of this species, we conducted conventional chromosome staining, C-banding, $ CMA_{3} $/DAPI fluorochromes, and in situ hybridization with a telomere probe in samples from Argentina. Most specimens had the standard karyotype 2n = 24, although numerical variations due to aneuploidies and supernumerary (B) chromosomes were detected. We registered novel structural polymorphisms for pair 11 and sex chromosomes, and a rearrangement involving pairs 2 and 4, possibly due to a spontaneous chromosomal mutation. Most A. montensis females are homogametic with XX sex chromosomes, although XY and X0 females were observed. Most individuals carrying B chromosomes had 1 B and, to a lesser extent, 2 and 3 B. The chromosomal variability detected at the southern limit of A. montensis distribution is high and similar to other geographically distant populations, despite the fact that it could be a region recently colonized. Some of these variations are unique and could have originated independently in southern populations, while others are shared throughout the species distribution and may have originated earlier. Aneuploidy (dpeaa)DE-He213 chromosomal rearrangement (dpeaa)DE-He213 sex-chromosomes polymorphism (dpeaa)DE-He213 supernumerary chromosomes (dpeaa)DE-He213 evolution (dpeaa)DE-He213 rodent (dpeaa)DE-He213 Ferro, Juan M. aut Buschiazzo, Leandro aut De Cena, Romina aut Kleiniving, Marcelo aut García, Gabriela aut Calcena, Eugenio aut Bolzan, Alejandro aut Lanzone, Cecilia aut Enthalten in Mammal research Heidelberg : Springer, 2015 68(2023), 3 vom: 13. Apr., Seite 355-365 (DE-627)817359311 (DE-600)2808353-2 2199-241X nnns volume:68 year:2023 number:3 day:13 month:04 pages:355-365 https://dx.doi.org/10.1007/s13364-023-00687-1 lizenzpflichtig 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_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 68 2023 3 13 04 355-365 |
allfieldsSound |
10.1007/s13364-023-00687-1 doi (DE-627)SPR051849461 (SPR)s13364-023-00687-1-e DE-627 ger DE-627 rakwb eng Labaroni, Carolina A. verfasserin (orcid)0000-0001-5255-0897 aut Extraordinary chromosome diversity in the southernmost populations of the montane grass mouse Akodon montensis (Cricetidae, Sigmodontinae) 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Mammal Research Institute Polish Academy of Sciences 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract Akodon montensis is abundant and widely distributed in the Atlantic Forest, which southern limits extends to northern Argentina, principally in the Misiones province. Chromosomal data from more centrally distributed populations in Brazil showed significant chromosome diversity; however, data from its southern boundaries are scarce. To explore the chromosomal diversity of this species, we conducted conventional chromosome staining, C-banding, $ CMA_{3} $/DAPI fluorochromes, and in situ hybridization with a telomere probe in samples from Argentina. Most specimens had the standard karyotype 2n = 24, although numerical variations due to aneuploidies and supernumerary (B) chromosomes were detected. We registered novel structural polymorphisms for pair 11 and sex chromosomes, and a rearrangement involving pairs 2 and 4, possibly due to a spontaneous chromosomal mutation. Most A. montensis females are homogametic with XX sex chromosomes, although XY and X0 females were observed. Most individuals carrying B chromosomes had 1 B and, to a lesser extent, 2 and 3 B. The chromosomal variability detected at the southern limit of A. montensis distribution is high and similar to other geographically distant populations, despite the fact that it could be a region recently colonized. Some of these variations are unique and could have originated independently in southern populations, while others are shared throughout the species distribution and may have originated earlier. Aneuploidy (dpeaa)DE-He213 chromosomal rearrangement (dpeaa)DE-He213 sex-chromosomes polymorphism (dpeaa)DE-He213 supernumerary chromosomes (dpeaa)DE-He213 evolution (dpeaa)DE-He213 rodent (dpeaa)DE-He213 Ferro, Juan M. aut Buschiazzo, Leandro aut De Cena, Romina aut Kleiniving, Marcelo aut García, Gabriela aut Calcena, Eugenio aut Bolzan, Alejandro aut Lanzone, Cecilia aut Enthalten in Mammal research Heidelberg : Springer, 2015 68(2023), 3 vom: 13. Apr., Seite 355-365 (DE-627)817359311 (DE-600)2808353-2 2199-241X nnns volume:68 year:2023 number:3 day:13 month:04 pages:355-365 https://dx.doi.org/10.1007/s13364-023-00687-1 lizenzpflichtig 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_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 68 2023 3 13 04 355-365 |
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Enthalten in Mammal research 68(2023), 3 vom: 13. Apr., Seite 355-365 volume:68 year:2023 number:3 day:13 month:04 pages:355-365 |
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Labaroni, Carolina A. @@aut@@ Ferro, Juan M. @@aut@@ Buschiazzo, Leandro @@aut@@ De Cena, Romina @@aut@@ Kleiniving, Marcelo @@aut@@ García, Gabriela @@aut@@ Calcena, Eugenio @@aut@@ Bolzan, Alejandro @@aut@@ Lanzone, Cecilia @@aut@@ |
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Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Akodon montensis is abundant and widely distributed in the Atlantic Forest, which southern limits extends to northern Argentina, principally in the Misiones province. Chromosomal data from more centrally distributed populations in Brazil showed significant chromosome diversity; however, data from its southern boundaries are scarce. To explore the chromosomal diversity of this species, we conducted conventional chromosome staining, C-banding, $ CMA_{3} $/DAPI fluorochromes, and in situ hybridization with a telomere probe in samples from Argentina. Most specimens had the standard karyotype 2n = 24, although numerical variations due to aneuploidies and supernumerary (B) chromosomes were detected. We registered novel structural polymorphisms for pair 11 and sex chromosomes, and a rearrangement involving pairs 2 and 4, possibly due to a spontaneous chromosomal mutation. Most A. montensis females are homogametic with XX sex chromosomes, although XY and X0 females were observed. Most individuals carrying B chromosomes had 1 B and, to a lesser extent, 2 and 3 B. The chromosomal variability detected at the southern limit of A. montensis distribution is high and similar to other geographically distant populations, despite the fact that it could be a region recently colonized. 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|
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Labaroni, Carolina A. |
spellingShingle |
Labaroni, Carolina A. misc Aneuploidy misc chromosomal rearrangement misc sex-chromosomes polymorphism misc supernumerary chromosomes misc evolution misc rodent Extraordinary chromosome diversity in the southernmost populations of the montane grass mouse Akodon montensis (Cricetidae, Sigmodontinae) |
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Extraordinary chromosome diversity in the southernmost populations of the montane grass mouse Akodon montensis (Cricetidae, Sigmodontinae) Aneuploidy (dpeaa)DE-He213 chromosomal rearrangement (dpeaa)DE-He213 sex-chromosomes polymorphism (dpeaa)DE-He213 supernumerary chromosomes (dpeaa)DE-He213 evolution (dpeaa)DE-He213 rodent (dpeaa)DE-He213 |
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misc Aneuploidy misc chromosomal rearrangement misc sex-chromosomes polymorphism misc supernumerary chromosomes misc evolution misc rodent |
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Extraordinary chromosome diversity in the southernmost populations of the montane grass mouse Akodon montensis (Cricetidae, Sigmodontinae) |
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Extraordinary chromosome diversity in the southernmost populations of the montane grass mouse Akodon montensis (Cricetidae, Sigmodontinae) |
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Labaroni, Carolina A. Ferro, Juan M. Buschiazzo, Leandro De Cena, Romina Kleiniving, Marcelo García, Gabriela Calcena, Eugenio Bolzan, Alejandro Lanzone, Cecilia |
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title_sort |
extraordinary chromosome diversity in the southernmost populations of the montane grass mouse akodon montensis (cricetidae, sigmodontinae) |
title_auth |
Extraordinary chromosome diversity in the southernmost populations of the montane grass mouse Akodon montensis (Cricetidae, Sigmodontinae) |
abstract |
Abstract Akodon montensis is abundant and widely distributed in the Atlantic Forest, which southern limits extends to northern Argentina, principally in the Misiones province. Chromosomal data from more centrally distributed populations in Brazil showed significant chromosome diversity; however, data from its southern boundaries are scarce. To explore the chromosomal diversity of this species, we conducted conventional chromosome staining, C-banding, $ CMA_{3} $/DAPI fluorochromes, and in situ hybridization with a telomere probe in samples from Argentina. Most specimens had the standard karyotype 2n = 24, although numerical variations due to aneuploidies and supernumerary (B) chromosomes were detected. We registered novel structural polymorphisms for pair 11 and sex chromosomes, and a rearrangement involving pairs 2 and 4, possibly due to a spontaneous chromosomal mutation. Most A. montensis females are homogametic with XX sex chromosomes, although XY and X0 females were observed. Most individuals carrying B chromosomes had 1 B and, to a lesser extent, 2 and 3 B. The chromosomal variability detected at the southern limit of A. montensis distribution is high and similar to other geographically distant populations, despite the fact that it could be a region recently colonized. Some of these variations are unique and could have originated independently in southern populations, while others are shared throughout the species distribution and may have originated earlier. © The Author(s), under exclusive licence to Mammal Research Institute Polish Academy of Sciences 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
abstractGer |
Abstract Akodon montensis is abundant and widely distributed in the Atlantic Forest, which southern limits extends to northern Argentina, principally in the Misiones province. Chromosomal data from more centrally distributed populations in Brazil showed significant chromosome diversity; however, data from its southern boundaries are scarce. To explore the chromosomal diversity of this species, we conducted conventional chromosome staining, C-banding, $ CMA_{3} $/DAPI fluorochromes, and in situ hybridization with a telomere probe in samples from Argentina. Most specimens had the standard karyotype 2n = 24, although numerical variations due to aneuploidies and supernumerary (B) chromosomes were detected. We registered novel structural polymorphisms for pair 11 and sex chromosomes, and a rearrangement involving pairs 2 and 4, possibly due to a spontaneous chromosomal mutation. Most A. montensis females are homogametic with XX sex chromosomes, although XY and X0 females were observed. Most individuals carrying B chromosomes had 1 B and, to a lesser extent, 2 and 3 B. The chromosomal variability detected at the southern limit of A. montensis distribution is high and similar to other geographically distant populations, despite the fact that it could be a region recently colonized. Some of these variations are unique and could have originated independently in southern populations, while others are shared throughout the species distribution and may have originated earlier. © The Author(s), under exclusive licence to Mammal Research Institute Polish Academy of Sciences 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
abstract_unstemmed |
Abstract Akodon montensis is abundant and widely distributed in the Atlantic Forest, which southern limits extends to northern Argentina, principally in the Misiones province. Chromosomal data from more centrally distributed populations in Brazil showed significant chromosome diversity; however, data from its southern boundaries are scarce. To explore the chromosomal diversity of this species, we conducted conventional chromosome staining, C-banding, $ CMA_{3} $/DAPI fluorochromes, and in situ hybridization with a telomere probe in samples from Argentina. Most specimens had the standard karyotype 2n = 24, although numerical variations due to aneuploidies and supernumerary (B) chromosomes were detected. We registered novel structural polymorphisms for pair 11 and sex chromosomes, and a rearrangement involving pairs 2 and 4, possibly due to a spontaneous chromosomal mutation. Most A. montensis females are homogametic with XX sex chromosomes, although XY and X0 females were observed. Most individuals carrying B chromosomes had 1 B and, to a lesser extent, 2 and 3 B. The chromosomal variability detected at the southern limit of A. montensis distribution is high and similar to other geographically distant populations, despite the fact that it could be a region recently colonized. Some of these variations are unique and could have originated independently in southern populations, while others are shared throughout the species distribution and may have originated earlier. © The Author(s), under exclusive licence to Mammal Research Institute Polish Academy of Sciences 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
collection_details |
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container_issue |
3 |
title_short |
Extraordinary chromosome diversity in the southernmost populations of the montane grass mouse Akodon montensis (Cricetidae, Sigmodontinae) |
url |
https://dx.doi.org/10.1007/s13364-023-00687-1 |
remote_bool |
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author2 |
Ferro, Juan M. Buschiazzo, Leandro De Cena, Romina Kleiniving, Marcelo García, Gabriela Calcena, Eugenio Bolzan, Alejandro Lanzone, Cecilia |
author2Str |
Ferro, Juan M. Buschiazzo, Leandro De Cena, Romina Kleiniving, Marcelo García, Gabriela Calcena, Eugenio Bolzan, Alejandro Lanzone, Cecilia |
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doi_str |
10.1007/s13364-023-00687-1 |
up_date |
2024-07-04T00:05:29.347Z |
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score |
7.4003077 |