Live-Imaging and Image Processing of Shoot Apical Meristems of Arabidopsis thaliana

Author(s):  
G. Venugopala Reddy ◽  
A. Roy-Chowdhury
2012 ◽  
Vol 56 (4) ◽  
pp. 601-606 ◽  
Author(s):  
W. Xin ◽  
Z. Liu ◽  
Y. Song ◽  
T. Hou ◽  
F. Xiang

eLife ◽  
2016 ◽  
Vol 5 ◽  
Author(s):  
John Paul Alvarez ◽  
Chihiro Furumizu ◽  
Idan Efroni ◽  
Yuval Eshed ◽  
John L Bowman

Leaves are flat determinate organs derived from indeterminate shoot apical meristems. The presence of a specific leaf meristem is debated, as anatomical features typical of meristems are not present in leaves. Here we demonstrate that multiple NGATHA (NGA) and CINCINNATA-class-TCP (CIN-TCP) transcription factors act redundantly, shortly after leaf initiation, to gradually restrict the activity of a leaf meristem in Arabidopsis thaliana to marginal and basal domains, and that their absence confers persistent marginal growth to leaves, cotyledons and floral organs. Following primordia initiation, the restriction of the broadly acting leaf meristem to the margins is mediated by the juxtaposition of adaxial and abaxial domains and maintained by WOX homeobox transcription factors, whereas other marginal elaboration genes are dispensable for its maintenance. This genetic framework parallels the morphogenetic program of shoot apical meristems and may represent a relic of an ancestral shoot system from which seed plant leaves evolved.


2020 ◽  
Vol 39 (4) ◽  
pp. 543-552 ◽  
Author(s):  
Wen Jie Zhang ◽  
Li Ming Zhai ◽  
Hai Xia Yu ◽  
Jing Peng ◽  
Shan Shan Wang ◽  
...  

2012 ◽  
Vol 37 (12) ◽  
pp. 2251-2260
Author(s):  
Jing-Yu GUO ◽  
Zhi-Xiong CHEN ◽  
Bing-Yao YANG ◽  
Xin-Fen CHEN ◽  
Xiang-Dong LIU ◽  
...  

2006 ◽  
Vol 37 (6) ◽  
pp. 371-374 ◽  
Author(s):  
N. M. Kaznina ◽  
G. F. Laidinen ◽  
A. F. Titov

Development ◽  
1999 ◽  
Vol 126 (3) ◽  
pp. 469-481 ◽  
Author(s):  
K. Lynn ◽  
A. Fernandez ◽  
M. Aida ◽  
J. Sedbrook ◽  
M. Tasaka ◽  
...  

Several lines of evidence indicate that the adaxial leaf domain possesses a unique competence to form shoot apical meristems. Factors required for this competence are expected to cause a defect in shoot apical meristem formation when inactivated and to be expressed or active preferentially in the adaxial leaf domain. PINHEAD, a member of a family of proteins that includes the translation factor eIF2C, is required for reliable formation of primary and axillary shoot apical meristems. In addition to high-level expression in the vasculature, we find that low-level PINHEAD expression defines a novel domain of positional identity in the plant. This domain consists of adaxial leaf primordia and the meristem. These findings suggest that the PINHEAD gene product may be a component of a hypothetical meristem forming competence factor. We also describe defects in floral organ number and shape, as well as aberrant embryo and ovule development associated with pinhead mutants, thus elaborating on the role of PINHEAD in Arabidopsis development. In addition, we find that embryos doubly mutant for PINHEAD and ARGONAUTE1, a related, ubiquitously expressed family member, fail to progress to bilateral symmetry and do not accumulate the SHOOT MERISTEMLESS protein. Therefore PINHEAD and ARGONAUTE1 together act to allow wild-type growth and gene expression patterns during embryogenesis.


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