scholarly journals An inducible, modular system for spatio-temporal control of gene expression in stomatal guard cells

2009 ◽  
Vol 60 (14) ◽  
pp. 4129-4136 ◽  
Author(s):  
Tou Cheu Xiong ◽  
Cliona M. Hann ◽  
John P. Chambers ◽  
Marie Surget ◽  
Carl K.-Y. Ng
2013 ◽  
Vol 64 (11) ◽  
pp. 3361-3371 ◽  
Author(s):  
Fabio Rusconi ◽  
Fabio Simeoni ◽  
Priscilla Francia ◽  
Eleonora Cominelli ◽  
Lucio Conti ◽  
...  

2012 ◽  
Author(s):  
Christopher Wilson ◽  
Frédéric Padilla ◽  
Man Zhang ◽  
Nuria Vilaboa ◽  
Oliver Kripfgans ◽  
...  

2021 ◽  
Author(s):  
Dennis Reichert ◽  
Helena Schepers ◽  
Julian Simke ◽  
Horst Lechner ◽  
Wolfgang Dörner ◽  
...  

The spatial and temporal control of gene expression at the post-transcriptional level is essential in eukaryotic cells and developing multicellular organisms. In recent years optochemical and optogenetic tools have enabled...


2018 ◽  
Vol 9 (1) ◽  
Author(s):  
Jeremy Dufourt ◽  
Antonio Trullo ◽  
Jennifer Hunter ◽  
Carola Fernandez ◽  
Jorge Lazaro ◽  
...  

2021 ◽  
Author(s):  
Martine Da Rocha ◽  
Caroline Bournaud ◽  
Julie Dazeniere ◽  
Peter Thorpe ◽  
Clement Pellegrin ◽  
...  

Root-knot nematodes are the major contributor to the crop losses caused by nematodes. Root-knot nematodes secrete effectors into the plant, derived from two sets of pharyngeal gland cells, to manipulate host physiology and immunity. Successful completion of the life cycle, involving successive molts from egg to adult, covers morphologically and functionally distinct stages and will require precise control of gene expression, including effectors. The details of how root-knot nematodes regulate transcription remain sparse. Here, we report a life stage-specific transcriptome of Meloidogyne incognita. Combined with an available annotated genome, we explore the spatio-temporal regulation of gene expression. We reveal gene expression clusters and predicted functions that accompany the major developmental transitions. Focusing on effectors, we identify a putative cis-regulatory motif associated with expression in the dorsal glands: providing an insight into effector regulation. We combine the presence of this motif with several other criteria to predict a novel set of putative dorsal gland effectors. Finally, we show this motif, and thereby its utility, is broadly conserved across the Meloidogyne genus and termed it Mel-DOG. Taken together, we provide the first genome-wide analysis of spatio-temporal gene expression in a root-knot nematode, and identify a new set of candidate effector genes that will guide future functional analyses.


Development ◽  
1995 ◽  
Vol 121 (10) ◽  
pp. 3233-3243 ◽  
Author(s):  
X. Cui ◽  
C.Q. Doe

The precise temporal control of gene expression is critical for specifying neuronal identity in the Drosophila central nervous system (CNS). A particularly interesting class of genes are those expressed at stereotyped times during the cell lineage of identified neural precursors (neuroblasts): these are termed ‘sublineage’ genes. Although sublineage gene function is vital for CNS development, the temporal regulation of this class of genes has not been studied. Here we show that four genes (ming, even-skipped, unplugged and achaete) are expressed in specific neuroblast sublineages. We show that these neuroblasts can be identified in embryos lacking both neuroblast cytokinesis and cell cycle progression (string mutants) and in embryos lacking only neuroblast cytokinesis (pebble mutants). We find that the unplugged and achaete genes are expressed normally in string and pebble mutant embryos, indicating that temporal control is independent of neuroblast cytokinesis or counting cell cycles. In contrast, neuroblasts require cytokinesis to activate sublineage ming expression, while a single, identified neuroblast requires cell cycle progression to activate even-skipped expression. These results suggest that neuroblasts have an intrinsic gene regulatory hierarchy controlling unplugged and achaete expression, but that cell cycle- or cytokinesis-dependent mechanisms are required for ming and eve CNS expression.


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