CoChat
Sign Up
Cited by 31Chromosomal and Genetic VariationsGenetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesFish biology, ecology, and behavior

Multiple Sex Chromosomes and Evolutionary Relationships in Amazonian Catfishes: The Outstanding Model of the Genus Harttia (Siluriformes: Loricariidae)

Open access
Sassi, Francisco de M. C., Deon, Geize A., Moreira-Filho, Orlando, Vicari, Marcelo R., Bertollo, Luiz A. C., Liehr, Thomas, de Oliveira, Ezequiel Aguiar, Cioffi, Marcelo B.·2020·Genes
DOI 10.3390/genes11101179PMC PMC7600804
Open this paper in CoChat — free accountOpen PDF

Abstract

The armored Harttia catfishes present great species diversity and remarkable cytogenetic variation, including different sex chromosome systems. Here we analyzed three new species, H. duriventris, H. villasboas and H. rondoni, using both conventional and molecular cytogenetic techniques (Giemsa-staining and C-banding), including the mapping of repetitive DNAs using fluorescence in situ hybridization (FISH) and comparative genomic hybridization (CGH) experiments. Both H. duriventris and H. villasboas have 2n = ♀56/♂55 chromosomes, and an X1X1X2X2 /X1X2Y sex chromosome system, while a proto or neo-XY system is proposed for H. rondoni (2n = 54♀♂). Single motifs of 5S and 18S rDNA occur in all three species, with the latter being also mapped in the sex chromosomes. The results confirm the general evolutionary trend that has been noticed for the genus: an extensive variation on their chromosome number, single sites of rDNA sequences and the occurrence of multiple sex chromosomes. Comparative genomic analyses with another congeneric species, H. punctata, reveal that the X1X2Y sex chromosomes of these species share the genomic contents, indicating a probable common origin. The remarkable karyotypic variation, including sex chromosomes systems, makes Harttia a suitable model for evolutionary studies focusing on karyotype differentiation and sex chromosome evolution among lower vertebrates.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.3390/genes11101179

Cites

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • The chromosome karyotypes of various catfish species exhibit a range of diploid numbers (2n) from 2n=40 to 2n=62.

    “the chromosome karyotypes of various catfish species exhibit a range of diploid numbers (2n) from 2n=40 to 2n=62 (de MC Sassi et al., 2020; Legrande, 1981).”

    From Chromosome-level genome assembly of the glass catfish (<i>Kryptopterus vitreolus</i>) reveals molecular clues to its transparent phenotype (2024) · cites this paper as de MC Sassi et al., 2020

    The Introduction and Discussion §4.1 (pages unavailable) describe variation in diploid number among Harttia catfishes and give an upper value of 2n = 62. They give the lower value as 2n = 52 in females and 53 in males, not 40; the cited paper therefore does not support the claimed lower endpoint. (LLM, conf=0.87)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

No references could be resolved yet.

Research works printed but not linked: 75

  1. [1]Ferraris C.J. Checklist of Catfishes, Recent and Fossil (Osteichthyes: Siluriformes), and Catalogue of Siluriform Primary Types Magnolia Press Auckland, New Zealand 2007 9781869770587
  2. [3]Traldi J.B. Lui R.L. Martinez J.d.F. Vicari M.R. Nogaroto V. Filho O.M. Blanco D.R. Chromosomal distribution of the retroelements Rex1, Rex3 and Rex6 in species of the genus Harttia and Hypostomus (Siluriformes: Loricariidae) Neotrop. Ichthyol. 2019 17 1 10 10.1590/1982-0224-20190010 · DOI
  3. [4]De Oliveira J.C. Oyakawa O.T. New loricariid fishes from headwaters on Serra da Mantiqueira and Complexo do Espinhaço, Minas Gerais state, Brazil (Teleostei: Siluriformes: Loricariidae) Zootaxa 2019 4586 401 424 10.11646/zootaxa.4586.3.1 31716114 · DOI
  4. [5]Alves A.L. Oliveira C. Foresti F. Karyotype variability in eight species of the subfamilies Loricariinae and Ancistrinae (Teleostei, Siluriformes, Loricariidae) Caryologia 2003 56 57 63 10.1080/00087114.2003.10589308 · DOI
  5. [6]Kavalco K.F. Pazza R. Bertollo L.A.C. Moreira-Filho O. Heterochromatin characterization of four fish species of the family Loricariidae (Siluriformes) Hereditas 2004 141 237 242 10.1111/j.1601-5223.2004.01850.x 15703039 · DOI
  6. [7]Kavalco K.F. Pazza R. Bertollo L.A.C. Moreira-Filho O. Karyotypic diversity and evolution of Loricariidae (Pisces, Siluriformes) Heredity 2005 94 180 186 10.1038/sj.hdy.6800595 15562288 · DOI
  7. [8]Centofante L. Bertollo L.A.C. Moreira-Filho O. Cytogenetic characterization and description of an XX/XY1Y2 sex chromosome system in catfish Harttia carvalhoi (Siluriformes, Loricariidae) Cytogenet. Genome Res. 2006 112 320 324 10.1159/000089887 16484789 · DOI
  8. [10]Blanco D.R. Vicari M.R. Artoni R.F. Traldi J.B. Moreira-Filho O. Chromosomal Characterization of Armored Catfish Harttia longipinna (Siluriformes, Loricariidae): First Report of B Chromosomes in the Genus Zool. Sci. 2012 29 604 609 10.2108/zsj.29.604 22943785 · DOI
  9. [11]Blanco D.R. Vicari M.R. Lui R.L. Bertollo L.A.C. Traldi J.B. Moreira-Filho O. The role of the Robertsonian rearrangements in the origin of the XX/XY1Y2 sex chromosome system and in the chromosomal differentiation in Harttia species (Siluriformes, Loricariidae) Rev. Fish Biol. Fish. 2013 23 127 134 10.1007/s11160-012-9283-5 · DOI
  10. [12]Blanco D.R. Vicari M.R. Lui R.L. Artoni R.F. de Almeida M.C. Traldi J.B. Margarido V.P. Moreira-Filho O. Origin of the X1X1X2X2/X1X2Y sex chromosome system of Harttia punctata (Siluriformes, Loricariidae) inferred from chromosome painting and FISH with ribosomal DNA markers Genetica 2014 142 119 126 10.1007/s10709-014-9759-4 24577679 · DOI
  11. [13]Blanco D.R. Vicari M.R. Lui R.L. Traldi J.B. Bueno V. Martinez J.d.F. Brandão H. Oyakawa O.T. Moreira Filho O. Karyotype Diversity and Evolutionary Trends in Armored Catfish Species of the Genus Harttia (Siluriformes: Loricariidae) Zebrafish 2017 14 169 176 10.1089/zeb.2016.1377 28060676 · DOI
  12. [14]Cioffi M.B. Bertollo L.A.C. Garrido-Ramos M.A. Genome Dynamics V. Chromosomal Distribution and Evolution of Repetitive DNAs in Fish Genome Dyn. 2012 7 197 221 22759820
  13. [15]Barby F.F. Bertollo L.A.C. de Oliveira E.A. Yano C.F. Hatanaka T. Ráb P. Sember A. Ezaz T. Artoni R.F. Liehr T. Emerging patterns of genome organization in Notopteridae species (Teleostei, Osteoglossiformes) as revealed by Zoo-FISH and Comparative Genomic Hybridization (CGH) Sci. Rep. 2019 9 1112 10.1038/s41598-019-38617-4 30718776 PMC6361938 · DOI
  14. [16]de Menezes Cavalcante Sassi F. Aguiar de Oliveira E. Bertollo L.A.C. Nirchio M. Hatanaka T. Marinho M.M.F. Moreira-Filho O. Aroutiounian R. Liehr T. Al-Rikabi A.B.H. Chromosomal evolution and evolutionary relationships of Lebiasina species (Characiformes, Lebiasinidae) Int. J. Mol. Sci. 2019 20 2944 PMC6628269 31208145
  15. [17]de Moraes R.L.R. Sember A. Bertollo L.A. De Oliveira E.A. Rab P. Hatanaka T. Marinho M.M. Liehr T. Al-Rikabi A.B. Feldberg E. Comparative cytogenetics and neo-Y formation in small-sized fish species of the genus Pyrrhulina (Characiformes, Lebiasinidae) Front. Genet. 2019 10 1 13 10.3389/fgene.2019.00678 31428127 PMC6689988 · DOI
  16. [18]Toma G.A. De Moraes R.L.R. Sassi F.D.M.C. Bertollo L.A.C. De Oliveira E.A. Rab P. Sember A. Liehr T. Hatanaka T. Viana P.F. Cytogenetics of the small-sized fish, Copeina guttata (Characiformes, Lebiasinidae): Novel insights into the karyotype differentiation of the family PLoS ONE 2019 14 1 13 10.1371/journal.pone.0226746 PMC6922430 31856256 · DOI
  17. [19]Covain R. Fisch-Muller S. Oliveira C. Mol J.H. Montoya-Burgos J.I. Dray S. Molecular phylogeny of the highly diversified catfish subfamily Loricariinae (Siluriformes, Loricariidae) reveals incongruences with morphological classification Mol. Phylogenetics Evol. 2016 94 492 517 10.1016/j.ympev.2015.10.018 26516029 · DOI
  18. [20]Bertollo L.A.C. Cioffi M.d.B. Galetti P.M. Filho O.M. Contributions to the cytogenetics of the Neotropical fish fauna Comp. Cytogenet. 2017 11 665 690 10.3897/compcytogen.v11i4.14713 29114360 PMC5672326 · DOI
  19. [21]Sumner A.T. A simple technique for demonstrating centromeric heterochromatin Exp. Cell Res. 1972 75 304 306 10.1016/0014-4827(72)90558-7 4117921 · DOI
  20. [22]Pendás A.M. Móran P. Freije J.P. Garcia-Vásquez E. Chromosomal location and nucleotide sequence of two tandem repeats of the Atlantic salmon 5S rDNA Cytogenet. Genome Res. 1994 67 31 36 10.1159/000133792 8187548 · DOI
  21. [23]Cioffi M.d.B. Martins C. Centofante L. Jacobina U.P. Bertollo L.A.C. Chromosomal variability among allopatric populations of Erythrinidae fish Hoplias malabaricus: Mapping of three classes of repetitive DNAs Cytogenet. Genome Res. 2009 125 132 141 10.1159/000227838 19729917 · DOI
  22. [24]Kubat Z. Hobza R. Vyskot B. Kejnovský E. Microsatellite accumulation in the Y chromosome of Silene latifolia Genome 2008 51 350 356 10.1139/G08-024 18438438 · DOI
  23. [25]Yano C.F. Bertollo L.A.C. Cioffi M.B. Fish-FISH: Molecular cytogenetics in fish species Fluorescence in Situ Hybridization (FISH)- Application Guide Liehr T. Springer Berlin, Germany 2017 429 444
  24. [26]Sambrook J. Russell D.W. Molecular Cloning, A Laboratory Manual Cold Spring Harbor Laboratory Press New York, NY, USA 2001
  25. [27]Zwick M.S. Hanson R.E. Mcknight T.D. Islam-Faridi M.H. Stelly D.M. Wing R.A. Price H.J. A rapid procedure for the isolation of C 0 t-1 DNA from plants Genome 1997 40 138 142 10.1139/g97-020 18464813 · DOI
  26. [28]de Moraes R.L.R. Bertollo L.A.C. Marinho M.M.F. Yano C.F. Hatanaka T. Barby F.F. Troy W.P. Cioffi M.D.B. Evolutionary relationships and cytotaxonomy considerations in the genus Pyrrhulina (Characiformes, Lebiasinidae) Zebrafish 2017 14 536 546 10.1089/zeb.2017.1465 28767325 · DOI
  27. [29]Sassi F.M.C. Hatanaka T. Moraes R.L.R. Toma G.A. Oliveira E.A. Liehr T. Rab P. Bertollo L.A.C. Viana P.F. Feldberg E. An insight into the chromosomal evolution of Lebiasinidae (Teleostei, Characiformes) Genes 2020 11 365 PMC7254295 32231057
  28. [30]Symonová R. Sember A. Majtánová Z. Ráb P. Characterization of fish genome by GISH and CGH Fish Cytogenetic Techniques. Ray-Fin Fishes and Chondrichthyans Ozouf-Costaz C. Pisano E. Foresti F. de Almeida-Toledo L.F. CRC Press Boca Raton, FL, USA 2015 118 131
  29. [31]Levan A. Fredga K. Sandberg A.A. Nomenclature for centromeric position on chromosomes Hereditas 1964 52 201 220 10.1111/j.1601-5223.1964.tb01953.x · DOI
  30. [32]Karr J. James F.C. Eco-morphological configurations and convergent evolution in species and communities Ecology and Evolution of Communities Cody M.L. Diamond J.M. Harvard University Press Cambridge, UK 1975 258 291
  31. [33]Wainwright P.C. Reilly S.M. Ecological Morphology: Integrative Organismal Biology University of Chicago Press Chicago, IL, USA 1994
  32. [34]Pazza R. Kavalco K.F. Bertollo L.A.C. Chromosome polymorphism in Astyanax fasciatus (Teleostei, Characidae). 1. Karyotype analysis, Ag-NORs and mapping of the 18S and 5S ribosomal genes in sympatric karyotypes and their possible hybrid forms Cytogenet. Genome Res. 2006 112 313 319 10.1159/000089886 16484788 · DOI
  33. [35]Ferreira-Neto M. Artoni R. Vicari M. Moreira Filho O. Camacho J. Bakkali M. Oliveira C. Foresti F. Three sympatric karyomorphs in the fish Astyanax fasciatus (Teleostei, Characidae) do not seem to hybridize in natural populations Comp. Cytogenet. 2012 6 29 40 10.3897/compcytogen.v6i1.2151 24260650 PMC3833771 · DOI
  34. [36]Pazza R. Dergam J.A. Kavalco K.F. Trends in karyotype evolution in Astyanax (Teleostei, Characiformes, Characidae): Insights from molecular data Front. Genet. 2018 9 131 10.3389/fgene.2018.00131 29713335 PMC5911472 · DOI
  35. [37]Bertollo L.A.C. Born G.G. Dergam J.A. Fenocchio A.S. Moreira-Filho O. A biodiversity approach in the neotropical Erythrinidae fish, Hoplias malabaricus. Karyotypic survey, geographic distribution of cytotypes and cytotaxonomic considerations Chromosome Res. 2000 8 603 613 10.1023/A:1009233907558 11117356 · DOI
  36. [38]Vicari M.R. Artoni R.F. Bertollo L.A.C. Comparative cytogenetics of Hoplias malabaricus (Pisces, Erythrinidae): A population analysis in adjacent hydrographic basins Genet. Mol. Biol. 2005 110 103 110 10.1590/S1415-47572005000100018 · DOI
  37. [39]Ibagón N. Maldonado-Ocampo J.A. Cioffi M.d.B. Dergam J.A. Chromosomal Diversity of Hoplias malabaricus (Characiformes, Erythrinidae) Along the Magdalena River (Colombia—Northern South America) and Its Significance for the Neotropical Region Zebrafish 2020 17 211 219 10.1089/zeb.2019.1827 · DOI
  38. [41]Oyakawa O.T. Fichberg I. Py-Daniel L.R. Three new species of Harttia (Loricariidae: Loricariinae) from Serra do Cachimbo, Rio Xingu basin, Pará, Northern Brazil Zootaxa 2018 4387 75 90 10.11646/zootaxa.4387.1.3 29690486 · DOI
  39. [42]Birindelli J.L.O. Britski H.A. New species of the genus Leporinus Agassiz (Characiformes: Anostomidae) from the rio Curuá, rio Xingu basin, Serra do Cachimbo, Brazil, with comments on Leporinus reticulatus Neotrop. Ichthyol. 2009 7 1 10 10.1590/S1679-62252009000100001 · DOI
  40. [43]Netto-Ferreira A.L. Three new species of Lebiasina (Characiformes: Lebiasinidae) from the Brazilian shield border at Serra do Cachimbo, Pará, Brazil Neotrop. Ichthyol. 2012 10 487 498 10.1590/S1679-62252012000300002 · DOI
  41. [45]Meyne J. Ratliff R.L. Moyzis R.K. Conservation of the human telomere sequence (TTAGGG)n among vertebrates Proc. Natl. Acad. Sci. USA 1989 86 7049 7053 10.1073/pnas.86.18.7049 2780561 PMC297991 · DOI
  42. [46]de Freitas N.L. Al-Rikabi A.B.H. Bertollo L.A.C. Ezaz T. Yano C.F. de Oliveira E.A. Hatanaka T. de Bello Cioffi M. Early Stages of XY Sex Chromosomes Differentiation in the Fish Hoplias malabaricus (Characiformes, Erythrinidae) Revealed by DNA Repeats Accumulation Curr. Genom. 2017 19 216 226 10.2174/1389202918666170711160528 PMC5850510 29606909 · DOI
  43. [47]Gammerdinger W.J. Kocher T.D. Unusual Diversity of Sex Chromosomes in African Cichlid Fishes Genes 2018 9 480 10.3390/genes9100480 PMC6210639 30287777 · DOI
  44. [48]Kottler V. Schartl M. The Colorful Sex Chromosomes of Teleost Fish Genes 2018 9 233 10.3390/genes9050233 PMC5977173 29751562 · DOI
  45. [49]Schartl M. Schmid M. Nanda I. Dynamics of vertebrate sex chromosome evolution: From equal size to giants and dwarfs Chromosoma 2016 125 553 571 10.1007/s00412-015-0569-y 26715206 · DOI
  46. [50]Guiguen Y. Pasquier J. Fostier A. Bobe J. Evolution of Sex Hormone Binding Globulins Reveals Early Gene Duplication at the Root of Vertebrates bioRxiv 2020 10.1101/2020.07.02.184432 33058907 · DOI
  47. [51]Arai R. Fish Karyotypes: A Check List Springer Science & Business Media Heidelberg, Germany 2011
  48. [52]Devlin R.H. Nagahama Y. Sex determination and sex differentiation in fish: An overview of genetic, physiological, and environmental influences Aquaculture 2002 208 191 364 10.1016/S0044-8486(02)00057-1 · DOI
  49. [53]Pennell M.W. Kirkpatrick M. Otto S.P. Vamosi J.C. Peichel C.L. Valenzuela N. Kitano J. Y Fuse? Sex Chromosome Fusions in Fishes and Reptiles PLoS Genet. 2015 11 1 17 10.1371/journal.pgen.1005237 25993542 PMC4439076 · DOI
  50. [54]Kitano J. Peichel C.L. Turnover of sex chromosomes and speciation in fishes Environ. Biol. Fishes 2012 94 549 558 10.1007/s10641-011-9853-8 26069393 PMC4459657 · DOI · Paper page
  51. [55]Cioffi M.B. Bertollo L.A.C. Initial steps in XY chromosome differentiation in Hoplias malabaricus and the origin of an X1X2Y sex chromosome system in this fish group Heredity 2010 105 554 561 10.1038/hdy.2010.18 20216570 · DOI
  52. [56]Cioffi M.B. Camacho J.P.M. Bertollo L.A.C. Repetitive DNAs and differentiation of sex chromosomes in neotropical fishes Cytogenet. Genome Res. 2011 132 188 194 10.1159/000321571 21042005 · DOI
  53. [57]Bitencourt J.A. Sampaio I. Ramos R.T.C. Vicari M.R. Affonso P.R.A.D.M. First Report of Sex Chromosomes in Achiridae (Teleostei: Pleuronectiformes) with Inferences about the Origin of the Multiple X1X1X2X2/X1X2Y System and Dispersal of Ribosomal Genes in Achirus achirus Zebrafish 2017 14 90 95 10.1089/zeb.2016.1333 27676413 · DOI
  54. [58]Ferreira M. Garcia C. Matoso D.A. de Jesus I.S. Feldberg E. A new multiple sex chromosome system X1X1X2X2/X1Y1X2Y2 in Siluriformes: Cytogenetic characterization of Bunocephalus coracoideus (Aspredinidae) Genetica 2016 144 591 599 10.1007/s10709-016-9927-9 27687472 · DOI
  55. [59]Xu D. Sember A. Zhu Q. De Oliveira E.A. Liehr T. Al-Rikabi A.B.H. Xiao Z. Song H. De Bello Cioffi M. Deciphering the Origin and Evolution of the X1X2Y System in Two Closely-Related Oplegnathus Species (Oplegnathidae and Centrarchiformes) Int. J. Mol. Sci. 2019 20 3571 10.3390/ijms20143571 PMC6678977 31336568 · DOI
  56. [60]Reed K.M. Phillips R.B. Polymorphism of the nucleolus organizer region (NOR) on the putative sex chromosomes of Arctic char (Salvelinus alpinus) is not sex related Chromosome Res. 1997 5 221 227 10.1023/A:1018411417816 9244448 · DOI
  57. [61]Charlesworth D. Charlesworth B. Marais G. Steps in the evolution of heteromorphic sex chromosomes Heredity 2005 95 118 128 10.1038/sj.hdy.6800697 15931241 · DOI
  58. [62]Cioffi M.B. Moreira-Filho O. Almeida-Toledo L.F. Bertollo L.A.C. The contrasting role of heterochromatin in the differentiation of sex chromosomes: An overview from Neotropical fishes J. Fish Biol. 2012 80 2125 2139 10.1111/j.1095-8649.2012.03272.x 22551173 · DOI
  59. [63]Phillips B.C. Edmands S. Does the speciation clock tick more slowly in the absence of heteromorphic sex chromosomes? BioEssays 2012 34 166 169 10.1002/bies.201100164 22237778 · DOI
  60. [64]Poltronieri J. Marquioni V. Bertollo L.A.C. Kejnovsky E. Molina W.F. Liehr T. Cioffi M.B. Comparative chromosomal mapping of microsatellites in Leporinus species (Characiformes, Anostomidae): Unequal accumulation on the W chromosomes Cytogenet. Genome Res. 2013 142 40 45 10.1159/000355908 24217024 · DOI
  61. [65]Sabath N. Itescu Y. Feldman A. Meiri S. Mayrose I. Valenzuela N. Sex determination, longevity, and the birth and death of reptilian species Ecol. Evol. 2016 6 5207 5220 10.1002/ece3.2277 27551377 PMC4984498 · DOI
  62. [66]Yano C.F. Bertollo L.A.C. Liehr T. Troy W.P. Cioffi M.D.B. W Chromosome Dynamics in Triportheus Species (Characiformes, Triportheidae): An Ongoing Process Narrated by Repetitive Sequences J. Hered. 2016 107 342 348 10.1093/jhered/esw021 27036509 PMC4888443 · DOI
  63. [67]Viana P.F. Ezaz T. de Bello Cioffi M. Liehr T. Al-Rikabi A. Goll L.G. Rocha A.M. Feldberg E. Landscape of snake’ sex chromosomes evolution spanning 85 MYR reveals ancestry of sequences despite distinct evolutionary trajectories Sci. Rep. 2020 10 1 14 10.1038/s41598-020-69349-5 32719365 PMC7385105 · DOI
  64. [68]Moreira-Filho O. Bertollo L.A.C. Galetti P.M. Distribution of sex chromosome mechanisms in neotropical fish and description of a ZZ/ZW system in Parodon hilarii (Parodontidae) Caryologia 1993 46 115 125 10.1080/00087114.1993.10797253 · DOI
  65. [69]Ramirez J.L. Birindelli J.L. Carvalho D.C. Affonso P.R. Venere P.C. Ortega H. Carrillo-Avila M. Rodríguez-Pulido J.A. Galetti P.M. Jr. Revealing hidden diversity of the underestimated neotropical ichthyofauna: DNA barcoding in the recently described genus Megaleporinus (Characiformes: Anostomidae) Front. Genet. 2017 8 149 10.3389/fgene.2017.00149 29075287 PMC5643504 · DOI
  66. [70]Schemberger M.O. Bellafronte E. Nogaroto V. Almeida M.C. Schühli G.S. Artoni R.F. Moreira-Filho O. Vicari M.R. Differentiation of repetitive DNA sites and sex chromosome systems reveal closely related group in Parodontidae (Actinopterygii: Characiformes) Genetica 2011 139 1499 1508 10.1007/s10709-012-9649-6 22527690 · DOI
  67. [71]Pucci M.B. Nogaroto V. Bertollo L.A.C. Moreira-Filho O. Vicari M.R. The karyotypes and evolution of ZZ/ZW sex chromosomes in the genus Characidium (Characiformes, Crenuchidae) Comp. Cytogenet. 2018 12 421 10.3897/CompCytogen.v12i3.28736 30310546 PMC6177511 · DOI
  68. [72]Yano C.F. Bertollo L.A.C. Ezaz T. Trifonov V. Sember A. Liehr T. Cioffi M.B. Highly conserved Z and molecularly diverged W chromosomes in the fish genus Triportheus (Characiformes, Triportheidae) Heredity 2017 118 276 283 10.1038/hdy.2016.83 28000659 PMC5315523 · DOI
  69. [73]Cioffi M.D.B. Yano C.F. Sember A. Bertollo L.A.C. Chromosomal evolution in lower vertebrates: Sex chromosomes in neotropical fishes Genes 2017 8 258 10.3390/genes8100258 28981468 PMC5664108 · DOI
  70. [74]Takehana Y. Naruse K. Hamaguchi S. Sakaizumi M. Evolution of ZZ/ZW and XX/XY sex-determination systems in the closely related medaka species, Oryzias hubbsi and O. dancena Chromosoma 2007 116 463 470 10.1007/s00412-007-0110-z 17882464 · DOI
  71. [75]Tanaka K. Takehana Y. Naruse K. Hamaguchi S. Sakaizumi M. Evidence for different origins of sex chromosomes in closely related oryzias fishes: Substitution of the master sex-determining gene Genetics 2007 177 2075 2081 10.1534/genetics.107.075598 17947439 PMC2219477 · DOI
  72. [76]Mank J.E. Avise J.C. Evolutionary diversity and turn-over of sex determination in teleost fishes Sex. Dev. 2009 3 60 67 10.1159/000223071 19684451 · DOI
  73. [77]Schultheis C. Böhne A. Schartl M. Volff J.N. Galiana-Arnoux D. Sex determination diversity and sex chromosome evolution in poeciliid fish Sex. Dev. 2009 3 68 77 10.1159/000223072 19684452 · DOI
  74. [78]Cioffi M.B. Liehr T. Trifonov V. Molina W.F. Bertollo L.A.C. Independent sex chromosome evolution in lower vertebrates: A molecular cytogenetic overview in the erythrinidae fish family Cytogenet. Genome Res. 2013 141 186 194 10.1159/000354039 23919986 · DOI
  75. [79]Schartl M. Sex chromosome evolution in non-mammalian vertebrates Curr. Opin. Genet. Dev. 2004 14 634 641 10.1016/j.gde.2004.09.005 15531158 · DOI

Cited by

Sorted by citations

Authors
Sassi, F. D. M. C., Deon, G. A., Moreira-Filho, O., Vicari, M. R., Bertollo, L. A. C., Liehr, T., de Oliveira, E. A., & Cioffi, M. B.
Affiliations
  • Universidade Federal de São Carlos (BR)
  • Laboratório de Citogenética de Peixes, Departamento de Genética e Evolução, Universidade Federal de São, Carlos, São Carlos, SP 13565-905, Brazil
  • Universidade Estadual de Ponta Grossa (BR)
  • Jena University Hospital (DE)
  • Secretaria de Estado de Educação do Mato Grosso—SEDUC-MT, Cuiabá, MT 78049-909, Brazil
Corresponding author
Liehr, Thomas
ORCID
Venue
Genes
Publisher
MDPI AG
Published
2020-10-10
Volume
11
Issue
10
Pages
1179
ISSN
2073-4425 (ISSN-L)
DOI
10.3390/genes11101179
PMC
PMC7600804
OpenAlex
W3092002866
Cited by
31
References
0
Citations by year
2026: 2 · 2025: 4 · 2024: 5 · 2023: 6 · 2022: 9 · 2021: 4 · 2020: 1
FWCI
3.23
Type
journal article
Language
en
Open access
Licence
Locations
  • Genes (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • Conselho Nacional de Desenvolvimento Científico e Tecnológico (302449/2018-3)
  • Fundação de Amparo à Pesquisa do Estado de São Paulo (2018/22033-1, 2020/02681-9)
Topics
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Chromosomal and Genetic Variations
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
  • Physical Sciences › Environmental Science › Nature and Landscape Conservation › Fish biology, ecology, and behavior
Keywords
Harttia, Loricariidae, multiple sex chromosomes, sex chromosome evolution, karyotype differentiation, 5S rDNA, 18S rDNA, chromosome number variation, comparative genomic hybridization, fluorescence in situ hybridization, C-banding, Amazonian catfish
MeSH terms
Animals, Catfishes, DNA, Ribosomal, Karyotyping, Sex Chromosomes, Genetic Variation, Genome, Evolution, Molecular, Genomics

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review