ArticlePlant molecular biology2019
A GARP transcription factor anther dehiscence defected 1 (OsADD1) regulates rice anther dehiscence.
Article in Plant molecular biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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10 citing papers in PubMed, 26 citations in OpenAlex.
- Analysis of mechanisms underlying accelerated plant growth induced by NtGLK85 overexpression in tobacco.Scientific reports · 2025Article
- Genome-Wide Identification ofInternational journal of molecular sciences · 2025Article
- OsKANADI1 and OsYABBY5 regulate rice plant height by targeting GIBERELLIN 2-OXIDASE6.The Plant cell · 2024Article
- A genome‑wide approach to the systematic and comprehensive analysis of LIM gene family in sorghum (Sorghum bicolor L.).Genomics & informatics · 2023Article
- The G2-Like gene family in Populus trichocarpa: identification, evolution and expression profiles.BMC genomic data · 2023Article
- Genome-Wide Identification and Characterization ofMolecules (Basel, Switzerland) · 2022Article
- A cascade of bHLH-regulated pathways programs maize anther development.The Plant cell · 2022Article
- Genome-wide characterization and analysis of Golden 2-Like transcription factors related to leaf chlorophyll synthesis in diploid and triploidFrontiers in plant science · 2022Article
- Genome-Wide Analysis of theFrontiers in genetics · 2021Article
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12 authors at 2 institutions in 1 country.
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Abstract
Anther dehiscence, one of the essential steps in pollination and double fertilization, is regulated by a complex signaling pathway encompassing hormones and environmental factors. However, key components underlying the signaling pathway that regulate anther dehiscence remain largely elusive. Here, we isolated a rice mutant anther dehiscence defected 1 (Osadd1) that exhibited defects in anther dehiscence and glume open. Map-based cloning revealed that OsADD1 encoded a GARP (Golden2, ARR-B and Psr1) transcription factor. Sequence analysis showed that a single base deletion in Osadd1 mutant resulted in pre-termination of the GARP domain. OsADD1 was constitutively expressed in various tissues, with more abundance in the panicles. The major genes associated with anther dehiscence were affected in the Osadd1 mutant, and the expression level of the cellulose synthase-like D sub-family 4 (OsCSLD4) was significantly decreased. We demonstrate that OsADD1 regulated the expression of OsCSLD4 by binding to its promoter, and affects rice anther dehiscence.
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