POPCORNFunctions in the Auxin Pathway to Regulate Embryonic Body Plan and Meristem Organization inArabidopsis

Author:

Xiang Daoquan1,Yang Hui1,Venglat Prakash1,Cao Yongguo1,Wen Rui2,Ren Maozhi1,Stone Sandra1,Wang Edwin3,Wang Hong2,Xiao Wei2,Weijers Dolf4,Berleth Thomas5,Laux Thomas6,Selvaraj Gopalan1,Datla Raju1

Affiliation:

1. Plant Biotechnology Institute, National Research Council Canada, Saskatoon, Saskatchewan S7N 0W9, Canada

2. University of Saskatchewan, Health Sciences Building, Saskatoon, Saskatchewan S7N 5E5, Canada

3. Biotechnology Research Institute, National Research Council Canada, Montreal, Quebec H4P 2R2, Canada

4. Wageningen University, Laboratory of Biochemistry, 6703 HA Wageningen, The Netherlands

5. Department of Botany, University of Toronto, Toronto, Ontario M5S 3B2, Canada

6. BIOSS, University of Freiburg, 79104 Freiburg, Germany

Abstract

AbstractThe shoot and root apical meristems (SAM and RAM) formed during embryogenesis are crucial for postembryonic plant development. We report the identification of POPCORN (PCN), a gene required for embryo development and meristem organization in Arabidopsis thaliana. Map-based cloning revealed that PCN encodes a WD-40 protein expressed both during embryo development and postembryonically in the SAM and RAM. The two pcn alleles identified in this study are temperature sensitive, showing defective embryo development when grown at 22°C that is rescued when grown at 29°C. In pcn mutants, meristem-specific expression of WUSCHEL (WUS), CLAVATA3, and WUSCHEL-RELATED HOMEOBOX5 is not maintained; SHOOTMERISTEMLESS, BODENLOS (BDL) and MONOPTEROS (MP) are misexpressed. Several findings link PCN to auxin signaling and meristem function: ectopic expression of DR5rev:green fluorescent protein (GFP), pBDL:BDL-GFP, and pMP:MP-β-glucuronidase in the meristem; altered polarity and expression of pPIN1:PIN1-GFP in the apical domain of the developing embryo; and resistance to auxin in the pcn mutants. The bdl mutation rescued embryo lethality of pcn, suggesting that improper auxin response is involved in pcn defects. Furthermore, WUS, PINFORMED1, PINOID, and TOPLESS are dosage sensitive in pcn, suggesting functional interaction. Together, our results suggest that PCN functions in the auxin pathway, integrating auxin signaling in the organization and maintenance of the SAM and RAM.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

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