{"id":1093172,"date":"2022-10-19T14:39:30","date_gmt":"2022-10-19T18:39:30","guid":{"rendered":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/uncategorized\/genome-wide-association-study-reveals-distinct-genetic-associations-related-to-leaf-hair-density-in-two-lineages-of-wheat-wild-relative-aegilops\/"},"modified":"2022-10-19T14:39:30","modified_gmt":"2022-10-19T18:39:30","slug":"genome-wide-association-study-reveals-distinct-genetic-associations-related-to-leaf-hair-density-in-two-lineages-of-wheat-wild-relative-aegilops","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/genome\/genome-wide-association-study-reveals-distinct-genetic-associations-related-to-leaf-hair-density-in-two-lineages-of-wheat-wild-relative-aegilops\/","title":{"rendered":"Genome-wide association study reveals distinct genetic associations related to leaf hair density in two lineages of wheat-wild relative Aegilops&#8230;"},"content":{"rendered":"<p><p>Solereder, H. Systematic Anatomy of the Dicotyledons: A Handbook for Laboratories of Pure and Applied Botany Vol. 2 (Clarendon Press, 1908).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Pesch, M. & Hlskamp, M. Creating a two-dimensional pattern de novo during Arabidopsis trichome and root hair initiation. Curr. Opin. Genet. Dev. 14, 422427 (2004).<\/p>\n<p>CAS    PubMed                        Google Scholar                <\/p>\n<p>Southwood, S. R. Plant surfaces and insectsAn overview. Insects Plant Surf. (eds Juniper, B & Southwood, S. R)  122 (Edward Arnold, 1986).<\/p>\n<p>Werker, E. Trichome diversity and development. 135 (2000).<\/p>\n<p>Duffey, S. S. Plant glandular trichomes: Their partial role in defence against insects. Insects Plant Surf. (eds Juniper, B & Southwood, S. R) 151172 (Edward Arnold, 1986).<\/p>\n<p>Hare, J. D. & Elle, E. Variable impact of diverse insect herbivores on dimorphic Datura wrightii. Ecology 83, 27112720 (2002).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Rautio, P. et al. Developmental plasticity in birch leaves: Defoliation causes a shift from glandular to nonglandular trichomes. Oikos 98, 437446 (2002).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Chassot, C. et al. Acetylation of cell wall is required for structural integrity of the leaf surface and exerts a global impact on plant stress responses. Front. Plant Sci. 6, 113 (2015).<\/p>\n<p>ADS                        Google Scholar                <\/p>\n<p>Hegebarth, D., Buschhaus, C., Wu, M., Bird, D. & Jetter, R. The composition of surface wax on trichomes of Arabidopsis thaliana differs from wax on other epidermal cells. Plant J. 88, 762774 (2016).<\/p>\n<p>CAS    PubMed                        Google Scholar                <\/p>\n<p>Choinski, J. S. Jr. & Wise, R. R. Leaf growth development in relation to gas exchange in quercus marilandica Muenchh. J. Plant Physiol. 154, 302309 (1999).<\/p>\n<p>CAS                        Google Scholar                <\/p>\n<p>Benz, B. W. & Martin, C. E. Foliar trichomes, boundary layers, and gas exchange in 12 species of epiphytic Tillandsia (Bromeliaceae). J. Plant Physiol. 163, 648656 (2006).<\/p>\n<p>CAS    PubMed                        Google Scholar                <\/p>\n<p>Baur, R., Binder, S. & Benz, G. Nonglandular leaf trichomes as short-term inducible defense of the grey alder, Alnus incana (L.), against the chrysomelid beetle, Agelastica alni L. Oecologia 87, 219226 (1991).<\/p>\n<p>ADS    CAS    PubMed                        Google Scholar                <\/p>\n<p>Agrawal, A. A. Induced responses to herbivory in wild radish: Effects on several herbivores and plant fitness. Ecology 80, 17131723 (1999).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Dalin, P. & Bjrkman, C. Adult beetle grazing induces willow trichome defence against subsequent larval feeding. Oecologia 134, 112118 (2003).<\/p>\n<p>ADS    PubMed                        Google Scholar                <\/p>\n<p>Yang, W. Y., Wu, B. H., Hu, X. R., Ye, Y. & Zhang, Y. Inheritance in hexaploid wheat of genes for hairy auricles and hairy leaf sheath derived from Aegilops tauschii Coss. Genet. Resour. Crop Evol. 46, 319323 (1999).<\/p>\n<p>CAS                        Google Scholar                <\/p>\n<p>Ehleringer, J. R. & Mooney, H. A. Leaf hairs: Effects on physiological activity and adaptive value to a desert shrub. Oecologia 37, 183200 (1978).<\/p>\n<p>ADS    CAS    PubMed                        Google Scholar                <\/p>\n<p>Maystrenko, O. I. Identification and localization of genes controlling leaf hairiness of young plants in common wheat. Russ. J. Genet. 12, 515 (1976).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Blanco, A. et al. A genetic linkage map of durum wheat. Theor. Appl. Genet. 97, 721728 (1998).<\/p>\n<p>CAS                        Google Scholar                <\/p>\n<p>Khlestkina, E. K. et al. Genetic mapping and tagging of wheat genes using RAPD, STS and SSR markers. Cell. Mol. Biol. Lett. 7, 795802 (2002).<\/p>\n<p>CAS    PubMed                        Google Scholar                <\/p>\n<p>Luo, W. et al. Genetic analysis of glume hairiness (Hg) gene in bread wheat (Triticum aestivum L). Genet. Resour. Crop Evol. 63, 763769 (2016).<\/p>\n<p>CAS                        Google Scholar                <\/p>\n<p>Taketa, S., Chang, C. L., Ishii, M. & Takeda, K. Chromosome arm location of the gene controlling leaf pubescence of a Chinese local wheat cultivar Hong-mang-mai. Euphytica 125, 141147 (2002).<\/p>\n<p>CAS                        Google Scholar                <\/p>\n<p>Shahinnia, F. et al. Identification of quantitative trait loci for leaf stomatal and epidermal cell traits in wheat (Triticum aestivum L.). In 12th International Wheat Genetic Symposium (2013).<\/p>\n<p>Dobrovolskaya, O. et al. Molecular mapping of genes determining hairy leaf character in common wheat with respect to other species of the Triticeae. Euphytica 155, 285293 (2007).<\/p>\n<p>CAS                        Google Scholar                <\/p>\n<p>Kihara, H. Discovery of the DD-analyzer, one of the ancestors of Triticum vulgare. Agric. Hortic. 19, 1314 (1944).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>McFadden, E. S. & Sears, E. R. The artificial synthesis of Triticum spelta. Rec. Genet. Soc. Am. 13, 2627 (1944).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Eig, A. Monographisch-kritische bersicht der Gattung Aegilops. Feddes Repert. Specierum Nov. Regni Veg. Beih. 55, 1228 (1929).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Hammer, K. Vorarbeiten zur monographischen Darstellung von Wildpflanzensortimenten: Aegilops L. Die Kult. 28, 33180 (1980).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Nishijima, R., Okamoto, Y., Hatano, H. & Takumi, S. Quantitative trait locus analysis for spikelet shape-related traits in wild wheat progenitor Aegilops tauschii: Implications for intraspecific diversification and subspecies differentiation. PLoS ONE 12, e0173210 (2017).<\/p>\n<p>PubMed    PubMed Central                        Google Scholar                <\/p>\n<p>Matsuoka, Y., Mori, N. & Kawahara, T. Genealogical use of chloroplast DNA variation for intraspecific studies of Aegilops tauschii Coss. Theor. Appl. Genet. 111, 265271 (2005).<\/p>\n<p>CAS    PubMed                        Google Scholar                <\/p>\n<p>Mahjoob, M. M. M. et al. Traits to differentiate lineages and subspecies of Aegilops tauschii, the D genome progenitor species of bread wheat. Diversity 13, 217 (2021).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Morihiro, H. & Takumi, S. Natural variation of trichome density on leaf in wild wheat Aegilops tauschii Coss. Wheat Inf. Serv. 109, 2010 (2010).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Liu, Y. et al. Genome-wide association study of 29 morphological traits in Aegilops tauschii. Sci. Rep. 5, 15562 (2015).<\/p>\n<p>ADS    CAS    PubMed    PubMed Central                        Google Scholar                <\/p>\n<p>Suwarno, W. B., Pixley, K. V., Palacios-Rojas, N., Kaeppler, S. M. & Babu, R. Genome-wide association analysis reveals new targets for carotenoid biofortification in maize. Theor. Appl. Genet. 128, 851864 (2015).<\/p>\n<p>CAS    PubMed    PubMed Central                        Google Scholar                <\/p>\n<p>Sun, C. et al. Genome-wide association study for 13 agronomic traits reveals distribution of superior alleles in bread wheat from the Yellow and Huai Valley of China. Plant Biotechnol. J. 15, 953969 (2017).<\/p>\n<p>CAS    PubMed    PubMed Central                        Google Scholar                <\/p>\n<p>Dvorak, J., Luo, M. C., Yang, Z. L. & Zhang, H. B. The structure of the Aegilops tauschii genepool and the evolution of hexaploid wheat. Theor. Appl. Genet. 97, 657670 (1998).<\/p>\n<p>CAS                        Google Scholar                <\/p>\n<p>Matsuoka, Y., Takumi, S. & Kawahara, T. Natural variation for fertile triploid F1 hybrid formation in allohexaploid wheat speciation. Theor. Appl. Genet. 115, 509518 (2007).<\/p>\n<p>PubMed                        Google Scholar                <\/p>\n<p>Matsuoka, Y. et al. Durum wheat cultivation associated with Aegilops tauschii in northern Iran. Genet. Resour. Crop Evol. 55, 861868 (2008).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Matsuoka, Y., Nishioka, E., Kawahara, T. & Takumi, S. Genealogical analysis of subspecies divergence and spikelet-shape diversification in central Eurasian wild wheat Aegilops tauschii Coss. Plant Syst. Evol. 279, 233244 (2009).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Aghaei, M. J., Mozafari, J., Taleei, A. R., Naghavi, M. R. & Omidi, M. Distribution and diversity of Aegilops tauschii in Iran. Genet. Resour. Crop Evol. 55, 341349 (2008).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Hamaoka, N. et al. A hairy-leaf gene, BLANKET LEAF, of wild Oryza nivara increases photosynthetic water use efficiency in rice. Rice 10, 1020 (2017).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Gorafi, Y. S., Kim, J. S., Elbashir, A. A. & Tsujimoto, H. A population of wheat multiple synthetic derivatives: An effective platform to explore, harness and utilize genetic diversity of Aegilops tauschii for wheat improvement. Theor. Appl. Genet. 131, 16151626 (2018).<\/p>\n<p>CAS    PubMed    PubMed Central                        Google Scholar                <\/p>\n<p>Chen, Z. et al. Detection of a major QTL conditioning trichome length and density on chromosome arm 4BL and development of near isogenic lines targeting this locus in bread wheat. Mol. Breed. 41, 19 (2021).<\/p>\n<p>CAS                        Google Scholar                <\/p>\n<p>Levy, A. A. & Feldman, M. Genetics of morphological traits in wild wheat, Triticum turgidum var. dicoccoides. Euphytica 40, 275281 (1989).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Yang, W. et al. Synthetic hexaploid wheat and its utilization for wheat genetic improvement in China. J. Genet. Genomics 36, 539546 (2009).<\/p>\n<p>CAS    PubMed                        Google Scholar                <\/p>\n<p>Li, J., Wan, H. S. & Yang, W. Y. Synthetic hexaploid wheat enhances variation and adaptive evolution of bread wheat in breeding processes. J. Syst. Evol. 52, 735742 (2014).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Huang, X. Q., Cster, H., Ganal, M. W. & Rder, M. S. Advanced backcross QTL analysis for the identification of quantitative trait loci alleles from wild relatives of wheat (Triticum aestivum L). Theor. Appl. Genet. 106, 13791389 (2003).<\/p>\n<p>CAS    PubMed                        Google Scholar                <\/p>\n<p>Huang, X. Q., Kempf, H., Ganal, M. W. & Rder, M. S. Advanced backcross QTL analysis in progenies derived from a cross between a German elite winter wheat variety and a synthetic wheat (Triticum aestivum L). Theor. Appl. Genet. 109, 933943 (2004).<\/p>\n<p>CAS    PubMed                        Google Scholar                <\/p>\n<p>Narasimhamoorthy, B., Gill, B. S., Fritz, A. K., Nelson, J. C. & Brown-Guedira, G. L. Advanced backcross QTL analysis of a hard winter wheat synthetic wheat population. Theor. Appl. Genet. 112, 787796 (2006).<\/p>\n<p>CAS    PubMed                        Google Scholar                <\/p>\n<p>Williams, K. & Sorrells, M. E. Three-dimensional seed size and shape QTL in hexaploid wheat (Triticum aestivum L.) populations. Crop Sci. 54, 98110 (2014).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Tsunewaki, K. Comparative gene analysis of common wheat and its ancestral species. II. Waxiness, growth habit and awnedness. Jpn. J. Bot. 19, 175229 (1966).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Wang, J. et al. Aegilops tauschii single nucleotide polymorphisms shed light on the origins of wheat D-genome genetic diversity and pinpoint the geographic origin of hexaploid wheat. New Phytol. 198, 925937 (2013).<\/p>\n<p>CAS    PubMed                        Google Scholar                <\/p>\n<p>Sohail, Q. et al. Applicability of Aegilops tauschii drought tolerance traits to breeding of hexaploid wheat. Breed. Sci. 61, 347357 (2011).<\/p>\n<p>CAS    PubMed    PubMed Central                        Google Scholar                <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>See the rest here:<br \/>\n<a target=\"_blank\" href=\"https:\/\/www.nature.com\/articles\/s41598-022-21713-3\" title=\"Genome-wide association study reveals distinct genetic associations related to leaf hair density in two lineages of wheat-wild relative Aegilops...\" rel=\"noopener\">Genome-wide association study reveals distinct genetic associations related to leaf hair density in two lineages of wheat-wild relative Aegilops...<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Solereder, H. Systematic Anatomy of the Dicotyledons: A Handbook for Laboratories of Pure and Applied Botany Vol <a href=\"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/genome\/genome-wide-association-study-reveals-distinct-genetic-associations-related-to-leaf-hair-density-in-two-lineages-of-wheat-wild-relative-aegilops\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":9,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[25],"tags":[],"class_list":["post-1093172","post","type-post","status-publish","format-standard","hentry","category-genome"],"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/1093172"}],"collection":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/users\/9"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/comments?post=1093172"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/1093172\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/media?parent=1093172"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/categories?post=1093172"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/tags?post=1093172"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}