ALTERED MERISTEM PROGRAM1 Suppresses Ectopic Stem Cell Niche Formation in the Shoot Apical Meristem in a Largely Cytokinin-Independent Manner. Issue 4 (11th February 2015)

• Record Type: Journal Article
• Authors: Huang, Wenwen; Pitorre, Delphine; Poretska, Olena; Marizzi, Christine; Winter, Nikola; Poppenberger, Brigitte; Sieberer, Tobias
• Is Part Of: Plant physiology. Volume 167:Issue 4(2015)
• Page Start: 1471
• Page End: 1486
• Publication Date: 2015-02-11
• Subjects: Plant physiology -- Periodicals; Botany -- Periodicals; Periodicals; Electronic journals; 571.2
• DOI: 10.1104/pp.114.254623
• Languages: English
• ISSNs: 0032-0889

Abstract

Abstract : Suppression of stem cell niche respecification in the shoot meristem periphery is mediated by a putative carboxypeptidase. Abstract: Plants are able to reiteratively form new organs in an environmentally adaptive manner during postembryonic development. Organ formation in plants is dependent on stem cell niches (SCN s), which are located in the so-called meristems. Meristems show a functional zonation along the apical-basal axis and the radial axis. Shoot apical meristems of higher plants are dome-like structures, which contain a central SCN that consists of an apical stem cell pool and an underlying organizing center. Organ primordia are formed in the circular peripheral zone (PZ ) from stem cell descendants in which differentiation programs are activated. One mechanism to keep this radial symmetry integrated is that the existing SCN actively suppresses stem cell identity in the PZ . However, how this lateral inhibition system works at the molecular level is far from understood. Here, we show that a defect in the putative carboxypeptidase ALTERED MERISTEM PROGRAM1 (AMP1) causes the formation of extra SCN s in the presence of an intact primary shoot apical meristem, which at least partially contributes to the enhanced shoot meristem size and leaf initiation rate found in the mutant. This defect appears to be neither a specific consequence of the altered cytokinin levels in amp1 nor directly mediated by the WUSCHEL/CLAVATA feedback loop. De novo formation of supernumerary stem cell pools was further enhanced in plants mutated in both AMP1 and its paralog LIKE AMP1, indicating that they exhibit partially overlapping roles to suppress SCN respecification in the PZ .