A system biology approach to discover novel transcriptional regulators that influence the Shoot growth by regulating cytokinin homeostasis in the shoot apical meristem of Arabidopsis thaliana
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IISER Mohali
Abstract
Sonal Yadav
PH14010
Thesis Abstract
A systems biology approach to discover novel transcriptional regulators
that influence the shoot growth by regulating cytokinin signal homeostasis
in the shoot apical meristem of Arabidopsis thaliana
Abstract:
Cytokinin (CK) signalling controls versatile functions in the shoot apical
meristem (SAM) of higher plants, such as stem cell niche maintenance, organ
patterning and differentiation of stem cells. Despite having comprehensive
knowledge of the shoot promoting role of CKs, very little is known about how
the spatio-temporal regulation of the genes encoding CK biosynthesis enzymes,
degradation enzymes and signalling factors in the shoot apical meristem (SAM)
is achieved. I have created the transcriptional reporters to determine the
expression pattern of CK genes in the SAM. Next, I have conducted a high-
throughput yeast-one-hybrid screen to determine the upstream transcriptional
regulators of the shoot specific CK biosynthesis, degradation and signalling
genes.
Based on the yeast-one-hybrid gene regulatory network, I identified transcription
factors that are either activated in response to hormone or abiotic stress and binds
to CK signalling gene promoters. NAC062/NAC WITH TRANSMEMBRANE
MOTIF1 (NTM1)-LIKE6 (NTL6) binds to the LONELY GUY4 (LOG4)
and ARABIDOPSIS HISTIDINE KINASE4 (AHK4). I have observed that CK
signalling output is decreased in the stem cell niche of nac062/ntl6 mutant plant
SAM, and as a result size of the shoot is also reduced. NAC062/NTL6 is
expressed throughout the SAM, and it has a minimal effect on the growth even in
the ambient conditions. Cold stress further stimulates NAC062/NTL6 cleavage
from the membrane, and thus, enters the nucleus where it activates the
transcription of LOG4 and AHK4. The ectopic expression of the constitutively
active NAC062/NTL6 resulted in delayed senescence and arrested shoot growth
due to increased cytokinin response. In summary, our work revealed an
interesting molecular link between NAC062/NTL6 and CK signalling
components.