Transcription Repressor HANABA TARANU Controls Flower Development by Integrating the Actions of Multiple Hormones, Floral Organ Specification Genes, and GATA3 Family Genes in Arabidopsis
Abstract
Plant inflorescence meristems and floral meristems possess specific boundary domains that result in proper floral organ separation and specification. HANABA TARANU (HAN) encodes a boundary-expressed GATA3-type transcription factor that regulates shoot meristem organization and flower development in Arabidopsis thaliana, but the underlying mechanism remains unclear. Through time-course microarray analyses following transient overexpression of HAN, we found that HAN represses hundreds of genes, especially genes involved in hormone responses and floral organ specification. Transient overexpression of HAN also represses the expression of HAN and three other GATA3 family genes, HANL2 (HAN-LIKE 2), GNC (GATA, NITRATE-INDUCIBLE, CARBON-METABOLISM-INVOLVED), and GNL (GNC-LIKE), forming a negative regulatory feedback loop. Genetic analysis indicates that HAN and the three GATA3 family genes coordinately regulate floral development, and their expression patterns are partially overlapping. HAN can homodimerize and heterodimerize with the three proteins encoded by these genes, and HAN directly binds to its own promoter and the GNC promoter in vivo. These findings, along with the fact that constitutive overexpression of HAN produces an even stronger phenotype than the loss-of-function mutation, support the hypothesis that HAN functions as a key repressor that regulates floral development via regulatory networks involving genes in the GATA3 family, along with genes involved in hormone action and floral organ specification.
Additional Information
© 2013 American Society of Plant Biologists. Received November 29, 2012; revised November 29, 2012; accepted December 28, 2012; published January 18, 2013. Published online before print January 2013. We thank members of the Meyerowitz lab for the discussion and technique help. We thank Xuemei Chen and Xigang Liu for help with the in situ hybridization, Wolfgang Lukowitz for communicating unpublished information, Arnavaz Garda for technical assistance, Adrienne Roeder for sharing constructs before publication, and Adrienne Roeder, Kaoru Sugimoto, An Yan, and Zachary Nimchuk for critical reading and comments on the article. This work was supported by National Institutes of Health Grant 1R01 GM086639 to E.M.M., by the National Basic Research of China 973 Program 2012CB113900 and National Natural Science Foundation of China 31171399 to X.Z., and by a California Institute of Technology Gosney Postdoctoral Fellowship to Y.Z. Author Contributions: X.Z. and Y.Z. conceived and performed most of the experiments and wrote the article along with E.M.M. L.D. did the real-time PCR for data verification. Z.W. and R.L. performed the microarray data analyses.Attached Files
Supplemental Material - tpc107854-Supplemental_Data_Set_1.xls
Supplemental Material - tpc107854Supplemental_Data.pdf
Files
Name | Size | Download all |
---|---|---|
md5:9a6c806275777d982443be46f15334d3
|
420.4 kB | Download |
md5:ac90b2bd14d1438f929562c8f22f888b
|
1.2 MB | Preview Download |
Additional details
- PMCID
- PMC3584552
- Eprint ID
- 37820
- Resolver ID
- CaltechAUTHORS:20130409-101033645
- NIH
- 1R01 GM086639
- National Basic Research of China 973 Program
- 2012CB113900
- National Natural Science Foundation of China
- 31171399
- Caltech Gosney Fellowship
- Created
-
2013-04-15Created from EPrint's datestamp field
- Updated
-
2021-11-09Created from EPrint's last_modified field