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Defective Kernel 1 ( DEK 1) is required for three‐dimensional growth in P hyscomitrella patens
Author(s) -
Perroud PierreFrançois,
Demko Viktor,
Johansen Wenche,
Wilson Robert C.,
Olsen OddArne,
Quatrano Ralph S.
Publication year - 2014
Publication title -
new phytologist
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.742
H-Index - 244
eISSN - 1469-8137
pISSN - 0028-646X
DOI - 10.1111/nph.12844
Subject(s) - protonema , physcomitrella patens , biology , mutant , microbiology and biotechnology , meristem , morphogenesis , cell division , botany , gene , genetics , moss , cell
Summary Orientation of cell division is critical for plant morphogenesis. This is evident in the formation and function of meristems and for morphogenetic transitions. Mosses undergo such transitions: from two‐dimensional tip‐growing filaments (protonema) to the generation of three‐dimensional leaf‐like structures (gametophores). The Defective Kernel 1 ( DEK 1) protein plays a key role in the perception of and/or response to positional cues that specify the formation and function of the epidermal layer in developing seeds of flowering plants. The moss P hyscomitrella patens contains the highly conserved DEK1 gene. Using efficient gene targeting, we generated a precise PpDEK1 deletion ( ∆dek1 ), which resulted in normal filamentous growth of protonema. Two distinct mutant phenotypes were observed: an excess of buds on the protonema, and abnormal cell divisions in the emerging buds resulting in developmental arrest and the absence of three‐dimensional growth. Overexpression of a complete PpDEK1 cDNA , or the calpain domain of PpDEK1 alone, successfully complements both phenotypes. These results in P . patens demonstrate the morphogenetic importance of the DEK 1 protein in the control of oriented cell divisions. As it is not for protonema, it will allow dissection of the structure/function relationships of the different domains of DEK 1 using gene targeting in null mutant background.

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