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Boundary domain genes were recruited to suppress bract growth and promote branching in maize
Grass inflorescence development is diverse and complex and involves sophisticated but poorly understood interactions of genes regulating branch determinacy and leaf growth. Here, we use a combination of transcript profiling and genetic and phylogenetic analyses to investigate tasselsheath1 (tsh1) an...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200273/ https://www.ncbi.nlm.nih.gov/pubmed/35704576 http://dx.doi.org/10.1126/sciadv.abm6835 |
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author | Xiao, Yuguo Guo, Jinyan Dong, Zhaobin Richardson, Annis Patterson, Erin Mangrum, Sidney Bybee, Seth Bertolini, Edoardo Bartlett, Madelaine Chuck, George Eveland, Andrea L. Scanlon, Michael J. Whipple, Clinton |
author_facet | Xiao, Yuguo Guo, Jinyan Dong, Zhaobin Richardson, Annis Patterson, Erin Mangrum, Sidney Bybee, Seth Bertolini, Edoardo Bartlett, Madelaine Chuck, George Eveland, Andrea L. Scanlon, Michael J. Whipple, Clinton |
author_sort | Xiao, Yuguo |
collection | PubMed |
description | Grass inflorescence development is diverse and complex and involves sophisticated but poorly understood interactions of genes regulating branch determinacy and leaf growth. Here, we use a combination of transcript profiling and genetic and phylogenetic analyses to investigate tasselsheath1 (tsh1) and tsh4, two maize genes that simultaneously suppress inflorescence leaf growth and promote branching. We identify a regulatory network of inflorescence leaf suppression that involves the phase change gene tsh4 upstream of tsh1 and the ligule identity gene liguleless2 (lg2). We also find that a series of duplications in the tsh1 gene lineage facilitated its shift from boundary domain in nongrasses to suppressed inflorescence leaves of grasses. Collectively, these results suggest that the boundary domain genes tsh1 and lg2 were recruited to inflorescence leaves where they suppress growth and regulate a nonautonomous signaling center that promotes inflorescence branching, an important component of yield in cereal grasses. |
format | Online Article Text |
id | pubmed-9200273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-92002732022-06-27 Boundary domain genes were recruited to suppress bract growth and promote branching in maize Xiao, Yuguo Guo, Jinyan Dong, Zhaobin Richardson, Annis Patterson, Erin Mangrum, Sidney Bybee, Seth Bertolini, Edoardo Bartlett, Madelaine Chuck, George Eveland, Andrea L. Scanlon, Michael J. Whipple, Clinton Sci Adv Biomedicine and Life Sciences Grass inflorescence development is diverse and complex and involves sophisticated but poorly understood interactions of genes regulating branch determinacy and leaf growth. Here, we use a combination of transcript profiling and genetic and phylogenetic analyses to investigate tasselsheath1 (tsh1) and tsh4, two maize genes that simultaneously suppress inflorescence leaf growth and promote branching. We identify a regulatory network of inflorescence leaf suppression that involves the phase change gene tsh4 upstream of tsh1 and the ligule identity gene liguleless2 (lg2). We also find that a series of duplications in the tsh1 gene lineage facilitated its shift from boundary domain in nongrasses to suppressed inflorescence leaves of grasses. Collectively, these results suggest that the boundary domain genes tsh1 and lg2 were recruited to inflorescence leaves where they suppress growth and regulate a nonautonomous signaling center that promotes inflorescence branching, an important component of yield in cereal grasses. American Association for the Advancement of Science 2022-06-15 /pmc/articles/PMC9200273/ /pubmed/35704576 http://dx.doi.org/10.1126/sciadv.abm6835 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Xiao, Yuguo Guo, Jinyan Dong, Zhaobin Richardson, Annis Patterson, Erin Mangrum, Sidney Bybee, Seth Bertolini, Edoardo Bartlett, Madelaine Chuck, George Eveland, Andrea L. Scanlon, Michael J. Whipple, Clinton Boundary domain genes were recruited to suppress bract growth and promote branching in maize |
title | Boundary domain genes were recruited to suppress bract growth and promote branching in maize |
title_full | Boundary domain genes were recruited to suppress bract growth and promote branching in maize |
title_fullStr | Boundary domain genes were recruited to suppress bract growth and promote branching in maize |
title_full_unstemmed | Boundary domain genes were recruited to suppress bract growth and promote branching in maize |
title_short | Boundary domain genes were recruited to suppress bract growth and promote branching in maize |
title_sort | boundary domain genes were recruited to suppress bract growth and promote branching in maize |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200273/ https://www.ncbi.nlm.nih.gov/pubmed/35704576 http://dx.doi.org/10.1126/sciadv.abm6835 |
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