Agriculture Reference
In-Depth Information
AtGLR
2.1 and
AtGLR
3.5 were downregulated.
At
GLR1.3 and
AtGLR
1.1
seemed not to respond at all to this stress hormone despite the latter being
implicated in the regulation of ABA biosynthesis and
antiAtGLR1.1
plants
exhibiting elevated ABA levels (Kang and Turano 2003; Sect. 3.3). Maathuis
et al. (2003) demonstrated that members of the
AtGLR
family showed time-
dependent changes in transcription in response to Ca
2+
deprivation and
excess Na
+
,butnotK
+
deprivation, supporting the prediction that they
function as NSCCs.
AnalysisofGUSexpressionundercontrolofthe
AtGLR3.4
promoter sug-
gested that
At
GLR3.4 expression was induced by mechanical stress such as
wounding or touch and cold (Meyerhoff et al. 2005). The upregulation of
AtGLR3.4
transcription by wounding and during senescence could suggest
an involvement of methyljasmonate (Sect. 13.3.1), a common component
of both processes (Devoto and Turner 2005). Quantitative RT-PCR analyses
of
At
GLR3.4 expression revealed that cold-induced transcription was fast,
reaching peak transcript levels after 30 min. Additionally, La
3+
inhibited
cold-induced
AtGLR3.4
transcription, suggesting the involvement of Ca
2+
.
AtGLR1.2
and
AtGLR2.5
are also upregulated by cold treatment (Zimmer-
mann et al. 2004).
13.4
Conclusions and Future Perspectives
Research into the glutamate receptor-like family has been hindered by the
lack of phenotypes associated with the
At
GLR genes. The novel pore region
of the predicted proteins and the paucity of understanding of NSCC func-
tion in vivo have made it difficult to predict function. However there are
now several phenotypes associated with
At
GLR overexpression (Kim et al.
2001) and knockout (Kang and Turano 2003; Kang et al. 2004), and system-
atic electrophysiological characterisation of single
At
GLR knockout plants
is underway (Qi et al. 2004, 2005; Gilliham 2005). Despite recent progress,
several fundamental questions still remain regarding
At
GLR function.
13.4.1
Expression
One promising approach to predicting
At
GLR function is the study of
At
GLR gene expression in response to developmental and environmental
cues. In particular, very rapid changes in gene expression in response to en-
vironmental signals (such as application of a ligand, or stresses) implicate
the gene product in specific responses to stimuli (Meyerhoff et al. 2004,
Search WWH ::
Custom Search