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Karyotype analysis of seven species of the tribe Lophiohylini (Hylinae, Hylidae, Anura), with conventional and molecular cytogenetic techniques
Few species of the tribe Lophiohylini have been karyotyped so far, and earlier analyses were performed mainly with standard staining. Based on the analysis of seven species with use of routine banding and molecular cytogenetic techniques, the karyotypes were compared and the cytogenetic data were ev...
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Published in: | Comparative cytogenetics 2012-01, Vol.6 (4), p.409-423 |
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description | Few species of the tribe Lophiohylini have been karyotyped so far, and earlier analyses were performed mainly with standard staining. Based on the analysis of seven species with use of routine banding and molecular cytogenetic techniques, the karyotypes were compared and the cytogenetic data were evaluated in the light of the current phylogenies. A karyotype with 2n = 24 and NOR in the chromosome 10 detected by Ag-impregnation and FISH with an rDNA probe was shared by Aparasphenodon bokermanni Miranda-Ribeiro, 1920, Itapotihyla langsdorffii (Duméril and Bibron, 1841), Trachycephalus sp., Trachycephalus mesophaeus (Hensel, 1867), and Trachycephalus typhonius (Linnaeus, 1758). Phyllodytes edelmoi Peixoto, Caramaschi et Freire, 2003 and Phyllodytes luteolus (Wied-Neuwied, 1824) had reduced the diploid number from 2n = 24 to 2n = 22 with one of the small-sized pairs clearly missing, and NOR in the large chromosome 2, but the karyotypes were distinct regarding the morphology of chromosome pairs 4 and 6. Based on the cytogenetic and phylogenetic data, it was presumed that the chromosome evolution occurred from an ancestral type with 2n = 24, in which a small chromosome had been translocated to one or more unidentified chromosomes. Whichever hypothesis is more probable, other rearrangements should have occurred later, to explain the karyotype differences between the two species of Phyllodytes Wagler, 1830. The majority of the species presented a small amount of centromeric C-banded heterochromatin and these regions were GC-rich. The FISH technique using a telomeric probe identified the chromosome ends and possibly (TTAGGG)n-like sequences in the repetitive DNA out of the telomeres in Itapotihyla langsdorffii and Phyllodytes edelmoi. The data herein obtained represent an important contribution for characterizing the karyotype variability within the tribe Lophiohylini scarcely analysed so far. |
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Based on the analysis of seven species with use of routine banding and molecular cytogenetic techniques, the karyotypes were compared and the cytogenetic data were evaluated in the light of the current phylogenies. A karyotype with 2n = 24 and NOR in the chromosome 10 detected by Ag-impregnation and FISH with an rDNA probe was shared by Aparasphenodon bokermanni Miranda-Ribeiro, 1920, Itapotihyla langsdorffii (Duméril and Bibron, 1841), Trachycephalus sp., Trachycephalus mesophaeus (Hensel, 1867), and Trachycephalus typhonius (Linnaeus, 1758). Phyllodytes edelmoi Peixoto, Caramaschi et Freire, 2003 and Phyllodytes luteolus (Wied-Neuwied, 1824) had reduced the diploid number from 2n = 24 to 2n = 22 with one of the small-sized pairs clearly missing, and NOR in the large chromosome 2, but the karyotypes were distinct regarding the morphology of chromosome pairs 4 and 6. Based on the cytogenetic and phylogenetic data, it was presumed that the chromosome evolution occurred from an ancestral type with 2n = 24, in which a small chromosome had been translocated to one or more unidentified chromosomes. Whichever hypothesis is more probable, other rearrangements should have occurred later, to explain the karyotype differences between the two species of Phyllodytes Wagler, 1830. The majority of the species presented a small amount of centromeric C-banded heterochromatin and these regions were GC-rich. The FISH technique using a telomeric probe identified the chromosome ends and possibly (TTAGGG)n-like sequences in the repetitive DNA out of the telomeres in Itapotihyla langsdorffii and Phyllodytes edelmoi. The data herein obtained represent an important contribution for characterizing the karyotype variability within the tribe Lophiohylini scarcely analysed so far.</description><identifier>ISSN: 1993-0771</identifier><identifier>EISSN: 1993-078X</identifier><identifier>DOI: 10.3897/CompCytogen.v6i4.3945</identifier><identifier>PMID: 24260681</identifier><language>eng</language><publisher>Bulgaria: Pensoft Publishers</publisher><subject>Banding ; Chromosome 10 ; Chromosome 2 ; Chromosomes ; Deoxyribonucleic acid ; DNA ; Gene sequencing ; Heterochromatin ; Karyotypes ; Morphology ; Nucleotide sequence ; Phyllodytes edelmoi ; Phylogeny ; Species ; Telomeres ; Trachycephalus</subject><ispartof>Comparative cytogenetics, 2012-01, Vol.6 (4), p.409-423</ispartof><rights>2012. This work is published under http://creativecommons.org/licenses/by/3.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Simone Lilian Gruber, Célio Fernando Baptista Haddad, Sanae Kasahara</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c572t-417d2c6ffe34bdc70856e3d694d9e5be8c5243ae71cbcab79656a1530a5296c53</citedby><cites>FETCH-LOGICAL-c572t-417d2c6ffe34bdc70856e3d694d9e5be8c5243ae71cbcab79656a1530a5296c53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834569/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2170364370?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24260681$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gruber, Simone Lilian</creatorcontrib><creatorcontrib>Haddad, Célio Fernando Baptista</creatorcontrib><creatorcontrib>Kasahara, Sanae</creatorcontrib><title>Karyotype analysis of seven species of the tribe Lophiohylini (Hylinae, Hylidae, Anura), with conventional and molecular cytogenetic techniques</title><title>Comparative cytogenetics</title><addtitle>Comp Cytogenet</addtitle><description>Few species of the tribe Lophiohylini have been karyotyped so far, and earlier analyses were performed mainly with standard staining. Based on the analysis of seven species with use of routine banding and molecular cytogenetic techniques, the karyotypes were compared and the cytogenetic data were evaluated in the light of the current phylogenies. A karyotype with 2n = 24 and NOR in the chromosome 10 detected by Ag-impregnation and FISH with an rDNA probe was shared by Aparasphenodon bokermanni Miranda-Ribeiro, 1920, Itapotihyla langsdorffii (Duméril and Bibron, 1841), Trachycephalus sp., Trachycephalus mesophaeus (Hensel, 1867), and Trachycephalus typhonius (Linnaeus, 1758). Phyllodytes edelmoi Peixoto, Caramaschi et Freire, 2003 and Phyllodytes luteolus (Wied-Neuwied, 1824) had reduced the diploid number from 2n = 24 to 2n = 22 with one of the small-sized pairs clearly missing, and NOR in the large chromosome 2, but the karyotypes were distinct regarding the morphology of chromosome pairs 4 and 6. Based on the cytogenetic and phylogenetic data, it was presumed that the chromosome evolution occurred from an ancestral type with 2n = 24, in which a small chromosome had been translocated to one or more unidentified chromosomes. Whichever hypothesis is more probable, other rearrangements should have occurred later, to explain the karyotype differences between the two species of Phyllodytes Wagler, 1830. The majority of the species presented a small amount of centromeric C-banded heterochromatin and these regions were GC-rich. The FISH technique using a telomeric probe identified the chromosome ends and possibly (TTAGGG)n-like sequences in the repetitive DNA out of the telomeres in Itapotihyla langsdorffii and Phyllodytes edelmoi. The data herein obtained represent an important contribution for characterizing the karyotype variability within the tribe Lophiohylini scarcely analysed so far.</description><subject>Banding</subject><subject>Chromosome 10</subject><subject>Chromosome 2</subject><subject>Chromosomes</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Gene sequencing</subject><subject>Heterochromatin</subject><subject>Karyotypes</subject><subject>Morphology</subject><subject>Nucleotide sequence</subject><subject>Phyllodytes edelmoi</subject><subject>Phylogeny</subject><subject>Species</subject><subject>Telomeres</subject><subject>Trachycephalus</subject><issn>1993-0771</issn><issn>1993-078X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkt9v0zAQxyMEYlPZnwCyxMuQ1mLHv-IXpKlibKISLyDxZjnOpXGVxsFOivJX8C_PWUvF8IN9Ot99fHf-Ztlbgle0UPLj2u_79TT4LXSrg3BsRRXjL7JLohRdYln8fHm2JbnIrmLc4bQ4K4jCr7OLnOUCi4JcZn--mjD5YeoBmc60U3QR-RpFOECHYg_WwZNjaAANwZWANr5vnG-m1nUOXd_Pp4EbNBvVbNx2YzAfbtBvNzTI-i6BBucTOz1Qob1vwY6tCcge64fBWTSAbTr3a4T4JntVmzbC1elcZD_uPn9f3y833748rG83S8tlPiwZkVVuRV0DZWVlJS64AFoJxSoFvITC8pxRA5LY0ppSKsGFIZxiw3MlLKeL7OHIrbzZ6T64fZqD9sbpJ4cPW21CKq0FXQKvCTUlAy5YZY2qMMGKWMULC6WZWZ-OrH4s91DZ1HAw7TPo85vONXrrD5oWlHGhEuD6BAh-HsKg9y5aaFvTgR-jJkyoHEsh8hT6_r_QnR9Dmm7UOZGYCkbTvsj4McoGH2OA-lwMwXpWkLZJQacf0LOC9KyglPfu307OWX_1Qh8BU9bJ0g</recordid><startdate>20120101</startdate><enddate>20120101</enddate><creator>Gruber, Simone Lilian</creator><creator>Haddad, Célio Fernando Baptista</creator><creator>Kasahara, Sanae</creator><general>Pensoft Publishers</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PATMY</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PYCSY</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20120101</creationdate><title>Karyotype analysis of seven species of the tribe Lophiohylini (Hylinae, Hylidae, Anura), with conventional and molecular cytogenetic techniques</title><author>Gruber, Simone Lilian ; Haddad, Célio Fernando Baptista ; Kasahara, Sanae</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c572t-417d2c6ffe34bdc70856e3d694d9e5be8c5243ae71cbcab79656a1530a5296c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Banding</topic><topic>Chromosome 10</topic><topic>Chromosome 2</topic><topic>Chromosomes</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Gene sequencing</topic><topic>Heterochromatin</topic><topic>Karyotypes</topic><topic>Morphology</topic><topic>Nucleotide sequence</topic><topic>Phyllodytes edelmoi</topic><topic>Phylogeny</topic><topic>Species</topic><topic>Telomeres</topic><topic>Trachycephalus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gruber, Simone Lilian</creatorcontrib><creatorcontrib>Haddad, Célio Fernando Baptista</creatorcontrib><creatorcontrib>Kasahara, Sanae</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Biological Sciences</collection><collection>Biological Science Database</collection><collection>Environmental Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Environmental Science Collection</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Comparative cytogenetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gruber, Simone Lilian</au><au>Haddad, Célio Fernando Baptista</au><au>Kasahara, Sanae</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Karyotype analysis of seven species of the tribe Lophiohylini (Hylinae, Hylidae, Anura), with conventional and molecular cytogenetic techniques</atitle><jtitle>Comparative cytogenetics</jtitle><addtitle>Comp Cytogenet</addtitle><date>2012-01-01</date><risdate>2012</risdate><volume>6</volume><issue>4</issue><spage>409</spage><epage>423</epage><pages>409-423</pages><issn>1993-0771</issn><eissn>1993-078X</eissn><abstract>Few species of the tribe Lophiohylini have been karyotyped so far, and earlier analyses were performed mainly with standard staining. Based on the analysis of seven species with use of routine banding and molecular cytogenetic techniques, the karyotypes were compared and the cytogenetic data were evaluated in the light of the current phylogenies. A karyotype with 2n = 24 and NOR in the chromosome 10 detected by Ag-impregnation and FISH with an rDNA probe was shared by Aparasphenodon bokermanni Miranda-Ribeiro, 1920, Itapotihyla langsdorffii (Duméril and Bibron, 1841), Trachycephalus sp., Trachycephalus mesophaeus (Hensel, 1867), and Trachycephalus typhonius (Linnaeus, 1758). Phyllodytes edelmoi Peixoto, Caramaschi et Freire, 2003 and Phyllodytes luteolus (Wied-Neuwied, 1824) had reduced the diploid number from 2n = 24 to 2n = 22 with one of the small-sized pairs clearly missing, and NOR in the large chromosome 2, but the karyotypes were distinct regarding the morphology of chromosome pairs 4 and 6. Based on the cytogenetic and phylogenetic data, it was presumed that the chromosome evolution occurred from an ancestral type with 2n = 24, in which a small chromosome had been translocated to one or more unidentified chromosomes. Whichever hypothesis is more probable, other rearrangements should have occurred later, to explain the karyotype differences between the two species of Phyllodytes Wagler, 1830. The majority of the species presented a small amount of centromeric C-banded heterochromatin and these regions were GC-rich. The FISH technique using a telomeric probe identified the chromosome ends and possibly (TTAGGG)n-like sequences in the repetitive DNA out of the telomeres in Itapotihyla langsdorffii and Phyllodytes edelmoi. The data herein obtained represent an important contribution for characterizing the karyotype variability within the tribe Lophiohylini scarcely analysed so far.</abstract><cop>Bulgaria</cop><pub>Pensoft Publishers</pub><pmid>24260681</pmid><doi>10.3897/CompCytogen.v6i4.3945</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Banding Chromosome 10 Chromosome 2 Chromosomes Deoxyribonucleic acid DNA Gene sequencing Heterochromatin Karyotypes Morphology Nucleotide sequence Phyllodytes edelmoi Phylogeny Species Telomeres Trachycephalus |
title | Karyotype analysis of seven species of the tribe Lophiohylini (Hylinae, Hylidae, Anura), with conventional and molecular cytogenetic techniques |
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