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An autoactive NB-LRR gene causes Rht13 dwarfism in wheat
- 1.0566545 - ÚEB 2024 RIV US eng J - Článek v odborném periodiku
Borrill, P. - Mago, R. - Xu, T. - Ford, B. A. - Williams, S. J. - Derkx, A. - Bovill, W. D. - Hyles, J. - Bhatt, D. - Xia, X. - MacMillan, C. - White, R. - Buss, W. - Molnár, István - Walkowiak, S. - Olsen, O.A. - Doležel, Jaroslav - Pozniak, C. - Spielmeyer, W.
An autoactive NB-LRR gene causes Rht13 dwarfism in wheat.
Proceedings of the National Academy of Sciences of the United States of America. Roč. 119, č. 48 (2022), č. článku e2209875119. ISSN 0027-8424. E-ISSN 1091-6490
Grant CEP: GA MŠMT(CZ) EF16_019/0000827
Institucionální podpora: RVO:61389030
Klíčová slova: autoactive NB-LRR * reduced-height (Rht) gene * semidwarfing gene * Triticum aestivum L. (wheat)
Obor OECD: Biochemistry and molecular biology
Impakt faktor: 11.1, rok: 2022 ; AIS: 4.488, rok: 2022
Způsob publikování: Open access
Web výsledku:
https://doi.org/10.1073/pnas.2209875119DOI: https://doi.org/10.1073/pnas.2209875119
Semidwarfing genes have greatly increased wheat yields globally, yet the widely used gibberellin (GA)-insensitive genes Rht-B1b and Rht-D1b have disadvantages for seedling emergence. Use of the GA-sensitive semidwarfing gene Rht13 avoids this pleiotropic effect. Here, we show that Rht13 encodes a nucleotide-binding site/leucine-rich repeat (NB-LRR) gene. A point mutation in the semidwarf Rht-B13b allele autoactivates the NB-LRR gene and causes a height reduction comparable with Rht-B1b and Rht-D1b in diverse genetic backgrounds. The autoactive Rht-B13b allele leads to transcriptional up-regulation of pathogenesis-related genes including class III peroxidases associated with cell wall remodeling. Rht13 represents a new class of reduced height (Rht) gene, unlike other Rht genes, which encode components of the GA signaling or metabolic pathways. This discovery opens avenues to use autoactive NB-LRR genes as semidwarfing genes in a range of crop species, and to apply Rht13 in wheat breeding programs using a perfect genetic marker.
Trvalý link: https://hdl.handle.net/11104/0337870Název souboru Staženo Velikost Komentář Verze Přístup 2022_Borrill_PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA_e2209875119.pdf 1 2.7 MB Jiná povolen
Počet záznamů: 1