BELL1-like homeobox genes regulate inflorescence architecture and meristem maintenance in rice.

BELL1-type transcription factor branch phyllotaxy homeobox gene inflorescence architecture internode meristem meristem maintenance micro-computer tomography scanning rice (Oryza sativa)

Journal

The Plant journal : for cell and molecular biology
ISSN: 1365-313X
Titre abrégé: Plant J
Pays: England
ID NLM: 9207397

Informations de publication

Date de publication:
05 2019
Historique:
received: 17 10 2018
revised: 26 12 2018
accepted: 10 01 2019
pubmed: 19 1 2019
medline: 28 4 2020
entrez: 19 1 2019
Statut: ppublish

Résumé

Inflorescence architecture is diverse in angiosperms, and is mainly determined by the arrangement of the branches and flowers, known as phyllotaxy. In rice (Oryza sativa), the main inflorescence axis, called the rachis, generates primary branches in a spiral phyllotaxy, and flowers (spikelets) are formed on these branches. Here, we have studied a classical mutant, named verticillate rachis (ri), which produces branches in a partially whorled phyllotaxy. Gene isolation revealed that RI encodes a BELL1-type homeodomain transcription factor, similar to Arabidopsis PENNYWISE/BELLRINGER/REPLUMLESS, and is expressed in the specific regions within the inflorescence and branch meristems where their descendant meristems would soon initiate. Genetic combination of an ri homozygote and a mutant allele of RI-LIKE1 (RIL1) (designated ri ril1/+ plant), a close paralog of RI, enhanced the ri inflorescence phenotype, including the abnormalities in branch phyllotaxy and rachis internode patterning. During early inflorescence development, the timing and arrangement of primary branch meristem (pBM) initiation were disturbed in both ri and ri ril1/+ plants. These findings suggest that RI and RIL1 were involved in regulating the phyllotactic pattern of the pBMs to form normal inflorescences. In addition, both RI and RIL1 seem to be involved in meristem maintenance, because the ri ril1 double-mutant failed to establish or maintain the shoot apical meristem during embryogenesis.

Identifiants

pubmed: 30657229
doi: 10.1111/tpj.14230
doi:

Substances chimiques

Plant Proteins 0

Banques de données

GENBANK
['LC417451', 'LC417452']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

465-478

Informations de copyright

© 2019 The Authors The Plant Journal © 2019 John Wiley & Sons Ltd.

Auteurs

Takuyuki Ikeda (T)

Department of Biological Sciences, School of Science, The University of Tokyo, Bunkyo-ku, Tokyo, 113-8654, Japan.

Wakana Tanaka (W)

Department of Biological Sciences, School of Science, The University of Tokyo, Bunkyo-ku, Tokyo, 113-8654, Japan.

Taiyo Toriba (T)

Department of Biological Sciences, School of Science, The University of Tokyo, Bunkyo-ku, Tokyo, 113-8654, Japan.

Chie Suzuki (C)

Department of Biological Sciences, School of Science, The University of Tokyo, Bunkyo-ku, Tokyo, 113-8654, Japan.

Akiteru Maeno (A)

National Institute of Genetics, Mishima, 411-8540, Japan.

Katsutoshi Tsuda (K)

National Institute of Genetics, Mishima, 411-8540, Japan.

Toshihiko Shiroishi (T)

National Institute of Genetics, Mishima, 411-8540, Japan.

Tetsuya Kurata (T)

Graduate School of Biological Sciences, Nara Institute of Science and Technology, Ikoma, 630-0192, Japan.

Tomoaki Sakamoto (T)

Graduate School of Biological Sciences, Nara Institute of Science and Technology, Ikoma, 630-0192, Japan.

Masayuki Murai (M)

Faculty of Agriculture and Marine Science, Kochi University, Monobe, Nankoku, 783-8502, Japan.

Hiroaki Matsusaka (H)

Faculty of Agriculture, Kyushu University, Motooka, 744, Fukuoka, 819-0395, Japan.

Toshihiro Kumamaru (T)

Faculty of Agriculture, Kyushu University, Motooka, 744, Fukuoka, 819-0395, Japan.

Hiro-Yuki Hirano (HY)

Department of Biological Sciences, School of Science, The University of Tokyo, Bunkyo-ku, Tokyo, 113-8654, Japan.

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Classifications MeSH