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Fig. 9.2.
NO modulates root architecture. Photographs of tomato seedlings incu-
bated in water (
control
), 1 mM of the NO scavenger 2-(4-carboxyphenyl)-4, 4,5,5-
tetramethylimidazoline-1-oxyl-3-oxide, potassium salt (
-NO
) and 200 µM of the NO donor
sodium nitroprusside (
+NO
)for5days.
Bar
:1cm.
Insets
Representative photographs of
fullyelongatedprimaryrootcells.
Bar
:50µm
showed that the NO-dependent reduction in primary root length correlates
with an inhibition in root cell elongation (Fig. 9.2, inset).
LRsoriginatefromazonedistaltotheactivelydividingprimaryroot
meristem. Hence, during the initiation of LRs, pericycle cells must dedif-
ferentiate and reenter the cell cycle. The plant hormone auxin promotes
theG1-to-Sphasetransitionthroughtheexpressionofcellcycleregulatory
genes like cyclins and cyclin-dependent kinases (CDK) in some pericycle
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