The shoot stem cell niche, contained within the shoot apical meristem (
- Award ID(s):
- 1640860
- NSF-PAR ID:
- 10033132
- Date Published:
- Journal Name:
- PHONONICS 2017: 4th International Conference on Phononic Crystals/Metamaterials, Phonon Transport/Coupling and Topological Phononics
- Page Range / eLocation ID:
- 102-103
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Summary SAM ) is maintained in Arabidopsis by the homeodomain proteinSHOOT MERISTEMLESS (STM ).STM is a mobile protein that traffics cell‐to‐cell, presumably through plasmodesmata. In maize, theSTM homologKNOTTED 1 shows clear differences betweenmRNA and protein localization domains in theSAM . However, theSTM mRNA and protein localization domains are not obviously different in Arabidopsis, and the functional relevance ofSTM mobility is unknown. Using a non‐mobile version ofSTM (2xNLS ‐YFP ‐STM ), we show thatSTM mobility is required to suppress axillary meristem formation during embryogenesis, to maintain meristem size, and to precisely specify organ boundaries throughout development. and organ boundary genesSTM (CUP SHAPED COTYLEDON 1 ),CUC 1 andCUC 2 regulate each other during embryogenesis to establish the embryonicCUC 3SAM and to specify cotyledon boundaries, andSTM controls expression post‐embryonically at organ boundary domains. We show that organ boundary specification by correct spatial expression ofCUC CUC genes requiresSTM mobility in the meristem. Our data suggest thatSTM mobility is critical for its normal function in shoot stem cell control. -
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