Artigo Acesso aberto Revisado por pares

A New Mode of Segregation in Gregory's Tetraploid Primulas

1914; University of Chicago Press; Volume: 48; Issue: 572 Linguagem: Inglês

10.1086/279426

ISSN

1537-5323

Autores

Hermann J. Müller,

Tópico(s)

Lichen and fungal ecology

Resumo

Previous article FreeNotes and LiteratureA New Mode of Segregation in Gregory's Tetraploid PrimulasHermann J. MullerHermann J. MullerPDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by The American Naturalist Volume 48, Number 572Aug., 1914 Published for The American Society of Naturalists Article DOIhttps://doi.org/10.1086/279426 Views: 164Total views on this site Citations: 67Citations are reported from Crossref PDF download Crossref reports the following articles citing this article:Seema Parveen, Nutan Singh, Arjun Adit, Suman Kumaria, Rajesh Tandon, Manu Agarwal, Arun Jagannath, Shailendra Goel Contrasting Reproductive Strategies of Two Nymphaea Species Affect Existing Natural Genetic Diversity as Assessed by Microsatellite Markers: Implications for Conservation and Wetlands Restoration, Frontiers in Plant Science 13 (Mar 2022).https://doi.org/10.3389/fpls.2022.773572Rafael Montalt, Laura Prósper, María Carmen Vives, Luis Navarro, Patrick Ollitrault, Pablo Aleza Breakdown of Self-Incompatibility in Citrus by Temperature Stress, Bud Pollination and Polyploidization, Agriculture 12, no.22 (Feb 2022): 273.https://doi.org/10.3390/agriculture12020273Nina Reis Soares, Marcelo Mollinari, Gleicy K. Oliveira, Guilherme S. Pereira, Maria Lucia Carneiro Vieira Meiosis in Polyploids and Implications for Genetic Mapping: A Review, Genes 12, no.1010 (Sep 2021): 1517.https://doi.org/10.3390/genes12101517Priyanka Sah, Sangeeta Mandal, Rajeev K. Singh, Nimisha Dutta, Ramashanker Sah, Abhinav Pathak, J.K. Srivastava, Achal Singh, Kuldeep K. Lal, Vindhya Mohindra Development of novel microsatellite marker panel in threatened tetraploid mahseer, Tor tor (Hamilton 1822) for insights into its genetic diversity and population structure, Meta Gene 28 (Jun 2021): 100880.https://doi.org/10.1016/j.mgene.2021.100880Kang Huang, Gwendolyn Huber, Kermit Ritland, Derek W Dunn, Baoguo Li, P Ingvarsson Performing parentage analysis for polysomic inheritances based on allelic phenotypes, G3 Genes|Genomes|Genetics 11, no.22 (Jan 2021).https://doi.org/10.1093/g3journal/jkaa064Wenqian Kong, Pheonah Nabukalu, T. Stan Cox, Valorie H. Goff, Gary J. Pierce, Cornelia Lemke, Jon S. Robertson, Rosana Compton, Haibao Tang, Andrew H. Paterson Transmission Genetics of a Sorghum bicolor × S. halepense Backcross Populations, Frontiers in Plant Science 11 (Apr 2020).https://doi.org/10.3389/fpls.2020.00467Miguel Garavello, José Cuenca, Andrés Garcia-Lor, Neus Ortega, Luis Navarro, Patrick Ollitrault, Pablo Aleza Male and female inheritance patterns in tetraploid 'Moncada' mandarin, Plant Cell Reports 39, no.33 (Nov 2019): 335–349.https://doi.org/10.1007/s00299-019-02494-yKang Huang, Derek W. Dunn, Kermit Ritland, Baoguo Li, Oscar Gaggiotti polygene : Population genetics analyses for autopolyploids based on allelic phenotypes, Methods in Ecology and Evolution 11, no.33 (Dec 2019): 448–456.https://doi.org/10.1111/2041-210X.13338Javier Do Canto, Bruno Studer, Ursula Frei, Thomas Lübberstedt, Odd Arne Rognli Pattern of inheritance of a self‐fertility gene in an autotetraploid perennial ryegrass ( Lolium perenne ) population, Plant Breeding 139, no.11 (Oct 2019): 207–213.https://doi.org/10.1111/pbr.12765Navid Mostafaee, Cortland K Griswold, Mark Chapman Two-Locus Local Adaptation by Additive or Epistatic Gene Combinations in Autotetraploids Versus Diploids, Journal of Heredity 110, no.77 (Dec 2019): 866–879.https://doi.org/10.1093/jhered/esz063Marcelo Mollinari, Antonio Augusto Franco Garcia Linkage Analysis and Haplotype Phasing in Experimental Autopolyploid Populations with High Ploidy Level Using Hidden Markov Models, G3 Genes|Genomes|Genetics 9, no.1010 (Oct 2019): 3297–3314.https://doi.org/10.1534/g3.119.400378Kang Huang, Tongcheng Wang, Derek W Dunn, Pei Zhang, Xiaoxiao Cao, Rucong Liu, Baoguo Li Genotypic Frequencies at Equilibrium for Polysomic Inheritance Under Double-Reduction, G3 Genes|Genomes|Genetics 9, no.55 (May 2019): 1693–1706.https://doi.org/10.1534/g3.119.400132Abdulqader Jighly, Zibei Lin, John W. Forster, German C. Spangenberg, Ben J. Hayes, Hans D. Daetwyler Insights into population genetics and evolution of polyploids and their ancestors, Molecular Ecology Resources 18, no.55 (May 2018): 1157–1172.https://doi.org/10.1111/1755-0998.12896Tanvir-Ul-Hassan Dar, Reiaz-Ul Rehman Occurrence of Polyploidy, (Nov 2017): 31–42.https://doi.org/10.1007/978-81-322-3772-3_3Joel R. Nguepjop, Hodo-Abalo Tossim, Joseph M. Bell, Jean-François Rami, Shivali Sharma, Brigitte Courtois, Nalini Mallikarjuna, Djibril Sane, Daniel Fonceka Evidence of Genomic Exchanges between Homeologous Chromosomes in a Cross of Peanut with Newly Synthetized Allotetraploid Hybrids, Frontiers in Plant Science 7 (Nov 2016).https://doi.org/10.3389/fpls.2016.01635P. Aleza, J. Cuenca, J. Juárez, L. Navarro, P. Ollitrault Inheritance in doubled-diploid clementine and comparative study with SDR unreduced gametes of diploid clementine, Plant Cell Reports 35, no.88 (Apr 2016): 1573–1586.https://doi.org/10.1007/s00299-016-1972-4Douglas E. Soltis, Clayton J. Visger, D. Blaine Marchant, Pamela S. Soltis Polyploidy: Pitfalls and paths to a paradigm, American Journal of Botany 103, no.77 (May 2016): 1146–1166.https://doi.org/10.3732/ajb.1500501Paul D. Blischak, Laura S. Kubatko, Andrea D. Wolfe Accounting for genotype uncertainty in the estimation of allele frequencies in autopolyploids, Molecular Ecology Resources 16, no.33 (Dec 2015): 742–754.https://doi.org/10.1111/1755-0998.12493K Huang, S T Guo, M R Shattuck, S T Chen, X G Qi, P Zhang, B G Li A maximum-likelihood estimation of pairwise relatedness for autopolyploids, Heredity 114, no.22 (Nov 2014): 133–142.https://doi.org/10.1038/hdy.2014.88Jennifer L Modliszewski, John H Willis Near-Absent Levels of Segregational Variation Suggest Limited Opportunities for the Introduction of Genetic Variation Via Homeologous Chromosome Pairing in Synthetic Neoallotetraploid Mimulus, G3 Genes|Genomes|Genetics 4, no.33 (Mar 2014): 509–522.https://doi.org/10.1534/g3.113.008441Pablo Aleza, Yann Froelicher, Sergio Schwarz, Manuel Agustí, María Hernández, José Juárez, François Luro, Raphael Morillon, Luis Navarro, Patrick Ollitrault Tetraploidization events by chromosome doubling of nucellar cells are frequent in apomictic citrus and are dependent on genotype and environment, Annals of Botany 108, no.11 (May 2011): 37–50.https://doi.org/10.1093/aob/mcr099D. W. Trapnell, J. L. Hamrick, K. C. Parker, K. W. Braungart, T. C. Glenn Evaluating the Utility of Microsatellites for Investigations of Autopolyploid Taxa, Journal of Heredity 102, no.44 (Jun 2011): 473–478.https://doi.org/10.1093/jhered/esr045M. STIFT, R. REEVE, P. H. Van TIENDEREN Inheritance in tetraploid yeast revisited: segregation patterns and statistical power under different inheritance models, Journal of Evolutionary Biology 23, no.77 (May 2010): 1570–1578.https://doi.org/10.1111/j.1420-9101.2010.02012.xMarc Stift, Camillo Berenos, Peter Kuperus, Peter H. van Tienderen Segregation Models for Disomic, Tetrasomic and Intermediate Inheritance in Tetraploids: A General Procedure Applied to Rorippa (Yellow Cress) Microsatellite Data, Genetics 179, no.44 (Aug 2008): 2113–2123.https://doi.org/10.1534/genetics.107.085027Z W Luo, Ze Zhang, Lindsey Leach, R M Zhang, John E Bradshaw, M J Kearsey Constructing Genetic Linkage Maps Under a Tetrasomic Model, Genetics 172, no.44 (Apr 2006): 2635–2645.https://doi.org/10.1534/genetics.105.052449JENNIFER A. TATE, DOUGLAS E. SOLTIS, PAMELA S. SOLTIS Polyploidy in Plants, (Jan 2005): 371–426.https://doi.org/10.1016/B978-012301463-4/50009-7Rongling Wu, Chang-Xing Ma, George Casella A Mixed Polyploid Model for Linkage Analysis in Outcrossing Tetraploids Using a Pseudo-Test Backcross Design, Journal of Computational Biology 11, no.44 (Aug 2004): 562–580.https://doi.org/10.1089/cmb.2004.11.562Rongling Wu, Maria Gallo-Meagher, Ramon C Littell, Zhao-Bang Zeng A General Polyploid Model for Analyzing Gene Segregation in Outcrossing Tetraploid Species, Genetics 159, no.22 (Oct 2001): 869–882.https://doi.org/10.1093/genetics/159.2.869Pamela S. Soltis, Douglas E. Soltis The role of genetic and genomic attributes in the success of polyploids, Proceedings of the National Academy of Sciences 97, no.1313 (Jun 2000): 7051–7057.https://doi.org/10.1073/pnas.97.13.7051D. V. Butruille, L. S. Boiteux Selection–mutation balance in polysomic tetraploids: Impact of double reduction and gametophytic selection on the frequency and subchromosomal localization of deleterious mutations, Proceedings of the National Academy of Sciences 97, no.1212 (May 2000): 6608–6613.https://doi.org/10.1073/pnas.100101097Salah M. Aljanabi Genetics, phylogenetics, and comparative genetics of Saccharum L., a polysomic polyploid Poales: Andropogoneae, (Jan 1998): 285–319.https://doi.org/10.1016/S1387-2656(08)70074-7R. C. Jackson, Jeff W. Jackson Gene segregation in autotetraploids: prediction from meiotic configurations, American Journal of Botany 83, no.66 (Jun 1996): 673–678.https://doi.org/10.1002/j.1537-2197.1996.tb12756.xJorge A. G. Da Silva, Bruno W. S. Sobral Genetics of Polyploids, (Jan 1996): 3–37.https://doi.org/10.1007/978-1-4615-9855-8_1K. G. Haynes, D. S. Douches Estimation of the coefficient of double reduction in the cultivated tetraploid potato, Theoretical and Applied Genetics 85-85, no.6-76-7 (Feb 1993): 857–862.https://doi.org/10.1007/BF00225029D. E. Soltis, P. S. Soltis, Loren H. Rieseberg Molecular Data and the Dynamic Nature of Polyploidy, Critical Reviews in Plant Sciences 12, no.33 (Mar 2011): 243–273.https://doi.org/10.1080/07352689309701903Pamela S. Soltis, Jeff J. Doyle, Douglas E. Soltis Molecular Data and Polyploid Evolution in Plants, (Jan 1992): 177–201.https://doi.org/10.1007/978-1-4615-3276-7_8Denis R. Featherstone, David J. Cove, Neil W. Ashton Genetic analysis by somatic hybridization of cytokinin overproducing developmental mutants of the moss,Physcomitrella patens, Molecular and General Genetics MGG 222, no.2-32-3 (Jul 1990): 217–224.https://doi.org/10.1007/BF00633821LOREN H. RIESEBERG, MICHAEL F. DOYLE Tetrasomic segregation in the naturally occurring autotetraploid Allium nevii (Alliaceae), Hereditas 111, no.11 (Feb 2008): 31–36.https://doi.org/10.1111/j.1601-5223.1989.tb00373.xDouglas E. Soltis, Pamela S. Soltis GENETIC CONSEQUENCES OF AUTOPOLYPLOIDY IN TOLMIEA (SAXIFRAGACEAE), Evolution 43, no.33 (May 2017): 586–594.https://doi.org/10.1111/j.1558-5646.1989.tb04254.xBryan D. Ness, Douglas E. Soltis, Pamela S. Soltis AUTOPOLYPLOIDY IN HEUCHERA MICRANTHA (SAXIFRAGACEAE), American Journal of Botany 76, no.44 (Apr 1989): 614–626.https://doi.org/10.1002/j.1537-2197.1989.tb11354.xDouglas E Soltis, Pamela S Soltis Electrophoretic evidence for tetrasomic segregation in Tolmiea menziesii (Saxifragaceae), Heredity 60, no.33 (Jun 1988): 375–382.https://doi.org/10.1038/hdy.1988.55Douglas E. Soltis, Loren H. Rieseberg AUTOPOLYPLOIDY IN TOLMIEA MENZIESII (SAXIFRAGACEAE): GENETIC INSIGHTS FROM ENZYME ELECTROPHORESIS, American Journal of Botany 73, no.22 (Feb 1986): 310–318.https://doi.org/10.1002/j.1537-2197.1986.tb08534.xG. G. Doyle The allotetraploidization of maize, Theoretical and Applied Genetics 54, no.44 (Jan 1979): 161–168.https://doi.org/10.1007/BF00263046G. G. Doyle Autotetraploid gene segregation, Theoretical and Applied Genetics 43, no.3-43-4 (Jan 1973): 139–146.https://doi.org/10.1007/BF00306563 Bibliography, (Jan 1973): 267–292.https://doi.org/10.1016/B978-0-12-406250-4.50017-9S. ELLERSTRÖM, A. HAGBERG MONOFACTORIAL HETEROSIS IN AUTOTETRAPLOID BARLEY, Hereditas 57, no.33 (Sep 2009): 319–326.https://doi.org/10.1111/j.1601-5223.1967.tb02113.xK.R. Dronamraju The Function of The Y-Chromosome in Man, Animals, and Plants, (Jan 1965): 227–310.https://doi.org/10.1016/S0065-2660(08)60050-4G. E. Van Dijk The inheritance of harsh leaves in tetraploid cocksfoot, Euphytica 13, no.33 (Oct 1964): 305–313.https://doi.org/10.1007/BF00023111W. Seyfffert Theoretische Untersuchungen über die Zusammensetzung tetrasomer Populationen. I. Panmixie, Biometrische Zeitschrift 2, no.11 (Jan 1960): 1–44.https://doi.org/10.1002/bimj.19600020102Thomas M. Little Gene segregation in autotetraploids. II, The Botanical Review 24, no.55 (May 1958): 318–339.https://doi.org/10.1007/BF02872438Urs Leupold Tetrad analysis oe segregation in autotetraploids, Journal of Genetics 54, no.33 (Nov 1956): 427–439.https://doi.org/10.1007/BF02982958H. C. J. Oomen Polyploidy in Canna, Genetica 24, no.11 (Dec 1949): 333–386.https://doi.org/10.1007/BF01487209Hilda Geiringer Contribution to the Heredity Theory of Multivalents, Journal of Mathematics and Physics 26, no.1-41-4 (Mar 2016): 246–278.https://doi.org/10.1002/sapm1947261246Thomas M. Little Gene segregation in autotetraploids, The Botanical Review 11, no.11 (Jan 1945): 60–85.https://doi.org/10.1007/BF02861164C. H. Cadman Autotetraploid-inheritance in the potato: Some new evidence, Journal of Genetics 44, no.11 (Sep 1942): 33–52.https://doi.org/10.1007/BF02982766E. W. Lindstrom Genetics of polyploidy, The Botanical Review 2, no.44 (Apr 1936): 197–215.https://doi.org/10.1007/BF02872444K. Mather Segregation and linkage in autotetraploids, Journal of Genetics 32, no.22 (Apr 1936): 287–314.https://doi.org/10.1007/BF02982683D. De Winton, J. B. S. Haldane The genetics ofPrimula sinensis, Journal of Genetics 31, no.11 (Jun 1935): 67–100.https://doi.org/10.1007/BF02982281W. J. C. Lawrence, Rose Scott-Honcrieff The genetics and chemistry of flower colour in Dahlia: A new theory of specific pigmentation, Journal of Genetics 30, no.22 (Mar 1935): 155–226.https://doi.org/10.1007/BF02982236K. Mather Reductional and equational separation of the chromosomes in bivalents and multivalents, Journal of Genetics 30, no.11 (Jan 1935): 53–78.https://doi.org/10.1007/BF02982205Aslaug Sverdrup Sömme Genetics and cytology of the tetraploid form ofPrimula sinensis, Journal of Genetics 23, no.33 (Dec 1930): 447–509.https://doi.org/10.1007/BF03161436J. B. S. Haldane Theoretical genetics of autopolyploids, Journal of Genetics 22, no.33 (Jul 1930): 359–372.https://doi.org/10.1007/BF02984197G. D. Karpechenko Polyploid hybrids ofRaphanus sativus L. XBrassica oleracea L, Zeitschrift für Induktive Abstammungs- und Vererbungslehre 48, no.11 (Dec 1928): 1–85.https://doi.org/10.1007/BF01740955M. B. Crane, C. D. Darlington The origin of new forms in Rubus, I, Genetica 9, no.4-64-6 (Jul 1927): 241–278.https://doi.org/10.1007/BF01508292 H. J. Muller Why Polyploidy is Rarer in Animals Than in Plants, The American Naturalist 59, no.663663 (Sep 2015): 346–353.https://doi.org/10.1086/280047 A. F. Blakeslee , John Belling , and M. E. Farnham Inheritance in Tetraploid Daturas, Botanical Gazette 76, no.44 (Oct 2015): 329–373.https://doi.org/10.1086/333268 Albert Francis Blakeslee Variations in Datura Due to Changes in Chromosome Number, The American Naturalist 56, no.642642 (Oct 2015): 16–31.https://doi.org/10.1086/279845

Referência(s)