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CLAVATA Was a Genetic Novelty for the Morphological Innovation of 3D Growth in Land Plants.

Current biology : CB (2018-07-24)
Chris D Whitewoods, Joseph Cammarata, Zoe Nemec Venza, Stephanie Sang, Ashley D Crook, Tsuyoshi Aoyama, Xiao Y Wang, Manuel Waller, Yasuko Kamisugi, Andrew C Cuming, Péter Szövényi, Zachary L Nimchuk, Adrienne H K Roeder, Michael J Scanlon, C Jill Harrison
ZUSAMMENFASSUNG

How genes shape diverse plant and animal body forms is a key question in biology. Unlike animal cells, plant cells are confined by rigid cell walls, and cell division plane orientation and growth rather than cell movement determine overall body form. The emergence of plants on land coincided with a new capacity to rotate stem cell divisions through multiple planes, and this enabled three-dimensional (3D) forms to arise from ancestral forms constrained to 2D growth. The genes involved in this evolutionary innovation are largely unknown. The evolution of 3D growth is recapitulated during the development of modern mosses when leafy shoots arise from a filamentous (2D) precursor tissue. Here, we show that a conserved, CLAVATA peptide and receptor-like kinase pathway originated with land plants and orients stem cell division planes during the transition from 2D to 3D growth in a moss, Physcomitrella. We find that this newly identified role for CLAVATA in regulating cell division plane orientation is shared between Physcomitrella and Arabidopsis. We report that roles for CLAVATA in regulating cell proliferation and cell fate are also shared and that CLAVATA-like peptides act via conserved receptor components in Physcomitrella. Our results suggest that CLAVATA was a genetic novelty enabling the morphological innovation of 3D growth in land plants.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
KOD Heißstart-DNA-Polymerase, High fidelity DNA polymerase designed for accurate PCR amplification of long strand and GC- rich DNA templates for cloning and cDNA amplification applications.
Roche
DIG-High Prime DNA-Markierungs- und Detektions-Starterkit II, sufficient for 12 labeling reactions (10 ng to 3 μg per assay), sufficient for 24 blots (blots of 100 cm2)