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Variations in Datura Due to Changes in Chromosome Number

1922; University of Chicago Press; Volume: 56; Issue: 642 Linguagem: Inglês

10.1086/279845

1537-5323

A. F. Blakeslee,

Chromosomal and Genetic Variations

Previous articleNext article FreeSymposium: The Origin of VariationsVariations in Datura Due to Changes in Chromosome NumberAlbert Francis BlakesleeAlbert Francis Blakeslee Search for more articles by this author PDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmailPrint SectionsMoreDetailsFiguresReferencesCited by The American Naturalist Volume 56, Number 642Jan. - Feb., 1922 Published for The American Society of Naturalists Article DOIhttps://doi.org/10.1086/279845 Views: 423Total views on this site Citations: 76Citations are reported from Crossref PDF download Crossref reports the following articles citing this article:Qun Feng, Junxing Yu, Jie Yu, Mingyang Hu, Lei Gu, Hongcheng Wang, Xuye Du, Bin Zhu, Mengxian Cai Identification and Genome-Wide Gene Expression Perturbation of a Trisomy in Chinese Kale (Brassica oleracea var. alboglabra), Plants 12, no.1818 (Sep 2023): 3199.https://doi.org/10.3390/plants12183199Yanbin Wen, Hongjiu Liu, Huanwen Meng, Lijun Qiao, Guoqing Zhang, Zhihui Cheng In vitro Induction and Phenotypic Variations of Autotetraploid Garlic (Allium sativum L.) 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Kaeppler, William Gordon-Kamm Maize transformation: history, progress, and perspectives, Molecular Breeding 41, no.66 (Jun 2021).https://doi.org/10.1007/s11032-021-01225-0Héloïse Bastiaanse, Isabelle M Henry, Helen Tsai, Meric Lieberman, Courtney Canning, Luca Comai, Andrew Groover A systems genetics approach to deciphering the effect of dosage variation on leaf morphology in Populus, The Plant Cell 33, no.44 (Nov 2020): 940–960.https://doi.org/10.1093/plcell/koaa016Guo Wen, Jiangbo Dang, Zhongyi Xie, Jinying Wang, Pengfei Jiang, Qigao Guo, Guolu Liang Molecular karyotypes of loquat (Eriobotrya japonica) aneuploids can be detected by using SSR markers combined with quantitative PCR irrespective of heterozygosity, Plant Methods 16, no.11 (Feb 2020).https://doi.org/10.1186/s13007-020-00568-7James R. Lupski 2018 Victor A. McKusick Leadership Award: Molecular Mechanisms for Genomic and Chromosomal Rearrangements, The American Journal of Human Genetics 104, no.33 (Mar 2019): 391–406.https://doi.org/10.1016/j.ajhg.2018.12.018Eric H. Reasor, James T. Brosnan, Robert N. Trigiano, J. Earl Elsner, Gerald M. Henry, Brian M. Schwartz The genetic and phenotypic variability of interspecific hybrid bermudagrasses (Cynodon dactylon (L.) Pers. × C. transvaalensis Burtt-Davy) used on golf course putting greens, Planta 244, no.44 (Jul 2016): 761–773.https://doi.org/10.1007/s00425-016-2573-8Nicola Williams Irene Manton, Erwin Schrödinger and the Puzzle of Chromosome Structure, Journal of the History of Biology 49, no.33 (Sep 2015): 425–459.https://doi.org/10.1007/s10739-015-9424-5Bin Zhu, Yujiao Shao, Qi Pan, Xianhong Ge, Zaiyun Li Genome-wide gene expression perturbation induced by loss of C2 chromosome in allotetraploid Brassica napus L., Frontiers in Plant Science 6 (Sep 2015).https://doi.org/10.3389/fpls.2015.00763James R. Lupski Structural variation mutagenesis of the human genome: Impact on disease and evolution, Environmental and Molecular Mutagenesis 56, no.55 (Apr 2015): 419–436.https://doi.org/10.1002/em.21943Kirsten Bomblies, Andreas Madlung Polyploidy in the Arabidopsis genus, Chromosome Research 22, no.22 (May 2014): 117–134.https://doi.org/10.1007/s10577-014-9416-xMaoyin Sheng, Lingjiao Wang, Xingjun Tian Identification of the full set of Fagopyrum esculentum trisomics by heterochromatin banding analysis and rDNA physical mapping, Scientia Horticulturae 155 (May 2013): 15–23.https://doi.org/10.1016/j.scienta.2013.02.027P K Sanyal, T E Wallis Valeriana Officinalis Linn., Its Polyploid Forms and the Structure of their Rhizomes and Roots, Journal of Pharmacy and Pharmacology 9, no.11 (Apr 2011): 162–175.https://doi.org/10.1111/j.2042-7158.1957.tb12269.xI. Rajcan, J.G. Boersma, E.J. Shaw Plant Genetic Techniques, (Jan 2011): 133–147.https://doi.org/10.1016/B978-0-08-088504-9.00252-XI. Rajcan, J.G. Boersma, E.J. Shaw Plant Genetic Techniques: Plant Breeder's Toolbox, (Jan 2011): 139–153.https://doi.org/10.1016/B978-0-444-64046-8.00219-6Isabelle M Henry, Brian P Dilkes, Eric S Miller, Diana Burkart-Waco, Luca Comai Phenotypic Consequences of Aneuploidy in Arabidopsis thaliana, Genetics 186, no.44 (Dec 2010): 1231–1245.https://doi.org/10.1534/genetics.110.121079K. R. Häntzschel, G. Weber Blockage of mitosis in maize root tips using colchicine-alternatives, Protoplasma 241, no.1-41-4 (Feb 2010): 99–104.https://doi.org/10.1007/s00709-009-0103-2Giovanni Neri, John M. Opitz Down syndrome: Comments and reflections on the 50th anniversary of Lejeune's discovery, American Journal of Medical Genetics Part A 149A, no.1212 (Nov 2009): 2647–2654.https://doi.org/10.1002/ajmg.a.33138Talukdar Dibyendu Cytogenetic characterization of seven different primary tetrasomics in grass pea ( Lathyrus sativus L.), Caryologia 61, no.44 (Feb 2014): 402–410.https://doi.org/10.1080/00087114.2008.10589654Isabelle M Henry, Brian P Dilkes, Luca Comai, John Doebley Genetic Basis for Dosage Sensitivity in Arabidopsis thaliana, PLoS Genetics 3, no.44 (Apr 2007): e70.https://doi.org/10.1371/journal.pgen.0030070Raphael Falk GENETIC ANALYSIS, (Jan 2007): 249–308.https://doi.org/10.1016/B978-044451543-8/50015-0Isabelle M. Henry, Brian P. Dilkes, Luca Comai Molecular karyotyping and aneuploidy detection in Arabidopsis thaliana using quantitative fluorescent polymerase chain reaction, The Plant Journal 48, no.22 (Sep 2006): 307–319.https://doi.org/10.1111/j.1365-313X.2006.02871.xIsabelle M. Henry, Brian P. Dilkes, Kim Young, Brian Watson, Helen Wu, Luca Comai Aneuploidy and Genetic Variation in the Arabidopsis thaliana Triploid Response, Genetics 170, no.44 (Jun 2005): 1979–1988.https://doi.org/10.1534/genetics.104.037788Jennifer L. Cooper, James A. Birchler Developmental impact on trans ‐acting dosage effects in maize aneuploids, genesis 31, no.22 (Oct 2001): 64–71.https://doi.org/10.1002/gene.10006Jeffrey L. Bennetzen, Chang-Nong Liu, Phillip SanMiguel, Patricia S. Springer, Young-Kwan Jin, Carolyn A. Zanta, Zoya Avramova Commonalities and Contrasts in the Organization of the Maize and Sorghum Nuclear Genomes, (Jan 1996): 103–113.https://doi.org/10.1007/978-1-4899-0280-1_8CH. Nagesh, N.C. Subrahmanyam Trisomics in Pearl Millet, Pennisetum Glaucum(L.) R.Br.: Development and Morphological Variation, Hereditas 123, no.33 (May 2004): 285–293.https://doi.org/10.1111/j.1601-5223.1995.t01-1-00285.xP. K. Sharma, A. K. Koul Genetic diversity among Plantagos III. Primary trisomy in Plantago lagopus L., Genetica 64, no.22 (Aug 1984): 135–138.https://doi.org/10.1007/BF00120264John M. Opitz, Jürgen Herrmann, James C. Pettersen, Edward T. Bersu, Sharon C. Colacino Terminological, Diagnostic, Nosological, and Anatomical-Developmental Aspects of Developmental Defects in Man, (Jan 1979): 71–164.https://doi.org/10.1007/978-1-4615-8276-2_2James M. Parry, Friedrich K. Zimmerman The detection of monosomic colonies produced by mitotic chromosome non-disjunction in the yeast Saccharomyces cerevisiae, Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 36, no.11 (Jul 1976): 49–66.https://doi.org/10.1016/0027-5107(76)90020-8Tibor Rajhathy TRISOMICS OF AVENA STRIGOSA, Canadian Journal of Genetics and Cytology 17, no.22 (Jun 1975): 151–166.https://doi.org/10.1139/g75-021H.H. SMITH, M.E. CONKLIN EFFECTS OF GENE DOSAGE ON PEROXIDASE ISOZYMES IN DATURA STRAMONIUM TRISOMICS, (Jan 1975): 603–618.https://doi.org/10.1016/B978-0-12-472703-8.50042-1Shafaat Mohammed Aneuploidy in guava, Biologia Plantarum 16, no.55 (Jun 2008): 382–388.https://doi.org/10.1007/BF02921004 Bibliography, (Jan 1973): 267–292.https://doi.org/10.1016/B978-0-12-406250-4.50017-9 References, (Jan 1972): 111–119.https://doi.org/10.1016/B978-0-433-18820-9.50022-5SVEN ASKER Apomixis and sexuality in the Potentilla argentea complex III. Euploid and aneuploid derivatives (including trisomics) of some apomictic biotypes, Hereditas 67, no.11 (Sep 2009): 111–142.https://doi.org/10.1111/j.1601-5223.1971.tb02365.xJ. G. Th. Hermsen Basic information for the use of primary trisomics in genetic and breeding research, Euphytica 19, no.22 (May 1970): 125–140.https://doi.org/10.1007/BF01902936O. P. Arora, T. N. Khoshoo Primary trisomics in Moss Verbena, Euphytica 18, no.22 (Sep 1969): 237–248.https://doi.org/10.1007/BF00035696Chi-Chang Chen, W. F. Grant MORPHOLOGICAL AND CYTOLOGICAL IDENTIFICATION OF THE PRIMARY TRISOMICS OF LOTUS PEDUNCULATUS (LEGUMINOSAE), Canadian Journal of Genetics and Cytology 10, no.11 (Mar 1968): 161–179.https://doi.org/10.1139/g68-023H Rees, G H Jones Chromosome evolution in Lolium, Heredity 22, no.11 (Feb 1967): 1–18.https://doi.org/10.1038/hdy.1967.1Frank C. Vasek PHENOTYPIC VARIATION IN TRISOMICS OF CLARKIA UNGUICULATA, American Journal of Botany 50, no.44 (Apr 1963): 308–314.https://doi.org/10.1002/j.1537-2197.1963.tb07197.xD. R. Sampson, A. W. S. Hunter, E. C. Bradley TRIPLOID × DIPLOID PROGENIES AND THE PRIMARY TRISOMICS OF ANTIRRHINUM MAJUS, Canadian Journal of Genetics and Cytology 3, no.22 (Jun 1961): 184–194.https://doi.org/10.1139/g61-022N. J. Hrishi Studies on the cytogenetics of six species of Pennisetums and their comparative morphology and anatomy, Genetica 26, no.11 (Dec 1953): 280–356.https://doi.org/10.1007/BF01690619T. S. Raghavan, A. R. Srinivasan Cytogenetical studies inDatura, Proceedings / Indian Academy of Sciences 15, no.11 (Jan 1942): 61–74.https://doi.org/10.1007/BF03049497T. H. Goodspeed, P. Avery Trisomic and other types inNicotiana sylvestris, Journal of Genetics 38, no.33 (Sep 1939): 381–458.https://doi.org/10.1007/BF02982757Albert F. Blakeslee, A. Dorothy Bergner, Amos G. Avery Geographical Distribution of Chromosomal Prime Types in Datura stramonium, CYTOLOGIA FujiiJubilaei, no.22 (Aug 1937): 1070–1093.https://doi.org/10.1508/cytologia.FujiiJubilaei.1070ARNE MüNTZING THE EFFECTS OF CHROMOSOMAL VARIATION IN DACTYLIS, Hereditas 23, no.1-21-2 (Jul 2010): 113–235.https://doi.org/10.1111/j.1601-5223.1937.tb02665.xE. W. SINNOTT, L. C. DUNN THE EFFECT OF GENES ON THE DEVELOPMENT OF SIZE AND FORM, Biological Reviews 10, no.22 (Jan 2008): 123–151.https://doi.org/10.1111/j.1469-185X.1935.tb00479.xD. McCullagh Chromosome and chromosome morphology in Plantaginaceae I, Genetica 16, no.1-21-2 (Jan 1934): 1–44.https://doi.org/10.1007/BF01837857G. Gazet Du Chatelier Un cas de “non-disjonction” dans le Sterculia platanifolia L., Bulletin de la Société Botanique de France 81, no.11 (Jul 2014): 136–138.https://doi.org/10.1080/00378941.1934.10833947R. Bauch Über die genetischen Grundlagen von Zwittrigkeit und neutralem Verhalten bei Brandpilzen, Planta 17, no.33 (Sep 1932): 612–640.https://doi.org/10.1007/BF01909772John T. Buchholz, Albert F. Blakeslee POLLEN‐TUBE GROWTH IN PRIMARY AND SECONDARY 2 n + 1 DATURAS, American Journal of Botany 19, no.77 (Jul 1932): 604–626.https://doi.org/10.1002/j.1537-2197.1932.tb08846.xnW. C. F. Newton, nCaroline Pellew Primula kewensis and its derivatives, Journal of Genetics 20, no.33 (Jan 1929): 405–467.https://doi.org/10.1007/BF02983158ARNE MÜNTZING CHROMOSOME NUMBER, NUCLEAR VOLUME AND POLLEN GRAIN SIZE IN GALEOPSIS, Hereditas 10, no.33 (Jul 2010): 241–260.https://doi.org/10.1111/j.1601-5223.1928.tb02473.x Margaret Mann Lesley , and Howard B. Frost Two Extreme "Small" Matthiola Plants: A Haploid with One and a Diploid with Two Additional Chromosome Fragments, The American Naturalist 62, no.678678 (Oct 2015): 22–33.https://doi.org/10.1086/280182C. D. Darlington Studies inPrunus, I and II, Journal of Genetics 19, no.22 (Jan 1928): 213–256.https://doi.org/10.1007/BF02984238Albert Francis Blakeslee NUBBIN, A COMPOUND CHROMOSOMAL TYPE IN DATURA, Annals of the New York Academy of Sciences 30, no.11 (Dec 2006): 1–29.https://doi.org/10.1111/j.1749-6632.1927.tb55358.xFritz von Wettstein Die Erscheinung der Heteroploidie, besonders im Pflanzenreich, (Jan 1927): 311–356.https://doi.org/10.1007/978-3-642-49712-4_5J. CLAUSEN GENETICAL AND CYTOLOGICAL INVESTIGATIONS ON VIOLA TRICOLOR L. AND V. ARVENSIS MURR, Hereditas 8, no.1-21-2 (Jul 2010): 1–156.https://doi.org/10.1111/j.1601-5223.1926.tb03159.xM. Senjaninova Das Verhalten des Nucleolus und der Trabanten w�hrend der somatischen Mitosen und den Reifeteilungen bei Ranunculus acer L., Zeitschrift f�r Zellforschung und Mikroskopische Anatomie 3, no.33 (Jan 1926): 417–427.https://doi.org/10.1007/BF00376581M. Nawaschin Variabilit�t des Zellkerns bei Crepis-Arten in bezug auf die Artbildung, Zeitschrift f�r Zellforschung und Mikroskopische Anatomie 4, no.22 (Jan 1926): 171–215.https://doi.org/10.1007/BF01094551W. de Mol De reductiedeeling bij eenige triticum-soorten, Genetica 6, no.11 (Dec 1924): 289–335.https://doi.org/10.1007/BF01501140F. Wettstein Morphologie und physiologie des formwechsels der moose auf genetischer grundlage. I, Zeitschrift für Induktive Abstammungs- und Vererbungslehre 33, no.11 (Dec 1924): 1–236.https://doi.org/10.1007/BF01762372 Howard B. Frost , and Margaret C. Mann Mutant Forms of Matthiola Resulting from Non-Disjunction, The American Naturalist 58, no.659659 (Oct 2015): 569–572.https://doi.org/10.1086/280010Ö. WINGE ZYTOLOGISCHE UNTERSUCHUNGEN ÜBER SPELTOIDE UND ANDERE MUTANTEN-ÄHNLICHE ABERRANTEN BEIM WEIZEN, Hereditas 5, no.33 (Jul 2010): 241–286.https://doi.org/10.1111/j.1601-5223.1924.tb03132.x 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 F. Blakeslee , and M. E. Farnham Trisomic Inheritance in the Poinsettia Mutant of Datura, The American Naturalist 57, no.653653 (Oct 2015): 481–495.https://doi.org/10.1086/279940M. B. Crane, A. E. Gairdner Species-crosses inCochlearia, with a preliminary account of their cytology, Journal of Genetics 13, no.22 (Aug 1923): 187–200.https://doi.org/10.1007/BF02983054E. LINDHARD FORTGESETZTE UNTERSUCHUNGEN ÜBER SPELTOIDMUTATIONEN, Hereditas 4, no.1-21-2 (Jul 2010): 206–220.https://doi.org/10.1111/j.1601-5223.1923.tb02958.x M. C. Coulter Origin of Variations, Botanical Gazette 74, no.22 (Oct 2015): 226–228.https://doi.org/10.1086/333083A. F. Blakeslee, John Belling, M. E. Farnham, A. Dorothy Bergner A Haploid Mutant in the Jimson Weed, " Datura stramonium ", Science 55, no.14331433 (Jun 1922): 646–647.https://doi.org/10.1126/science.55.1433.646J. T. Buchholz, A. F. Blakeslee STUDIES OF THE POLLEN TUBES AND ABORTIVE OVULES OF THE GLOBE MUTANT OF DATURA, Science 55, no.14311431 (Jun 1922): 597–599.https://doi.org/10.1126/science.55.1431.597