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Flavonol rhamnosylation indirectly modifies the cell wall defects of RHAMNOSE BIOSYNTHESIS1 mutants by altering rhamnose flux
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Abstract
Rhamnose is required in
Arabidopsis thaliana
for synthesizing pectic polysaccharides and glycosylating flavonols.
RHAMNOSE BIOSYNTHESIS1 (RHM1)
encodes a UDP-L-rhamnose synthase, and
rhm1
mutants exhibit many developmental defects, including short root hairs, hyponastic cotyledons, and left-handed helically twisted petals and roots. It has been proposed that the hyponastic cotyledons observed in
rhm1
mutants are a consequence of abnormal flavonol glycosylation, while the root hair defect is flavonol-independent. We have recently shown that the helical twisting of
rhm1
petals results from decreased levels of rhamnose-containing cell wall polymers. In this work, we find that flavonols indirectly modify the
rhm1
helical petal phenotype by altering rhamnose flux to the cell wall. Given this finding, we further investigated the relationship between flavonols and the cell wall in
rhm1
cotyledons. We show that decreased flavonol rhamnosylation is not responsible for the cotyledon phenotype of
rhm1
mutants. Instead, flavonols provide a large reservoir of rhamnose, and blocking flavonol synthesis or rhamnosylation can suppress
rhm1
defects by diverting rhamnose to the synthesis of cell wall polysaccharides. Therefore, rhamnose is required in the cell wall for normal expansion of cotyledon epidermal cells. Our findings suggest a broad role for rhamnose-containing cell wall polysaccharides in the morphogenesis of epidermal cells.
Title: Flavonol rhamnosylation indirectly modifies the cell wall defects of
RHAMNOSE BIOSYNTHESIS1
mutants by altering rhamnose flux
Description:
Abstract
Rhamnose is required in
Arabidopsis thaliana
for synthesizing pectic polysaccharides and glycosylating flavonols.
RHAMNOSE BIOSYNTHESIS1 (RHM1)
encodes a UDP-L-rhamnose synthase, and
rhm1
mutants exhibit many developmental defects, including short root hairs, hyponastic cotyledons, and left-handed helically twisted petals and roots.
It has been proposed that the hyponastic cotyledons observed in
rhm1
mutants are a consequence of abnormal flavonol glycosylation, while the root hair defect is flavonol-independent.
We have recently shown that the helical twisting of
rhm1
petals results from decreased levels of rhamnose-containing cell wall polymers.
In this work, we find that flavonols indirectly modify the
rhm1
helical petal phenotype by altering rhamnose flux to the cell wall.
Given this finding, we further investigated the relationship between flavonols and the cell wall in
rhm1
cotyledons.
We show that decreased flavonol rhamnosylation is not responsible for the cotyledon phenotype of
rhm1
mutants.
Instead, flavonols provide a large reservoir of rhamnose, and blocking flavonol synthesis or rhamnosylation can suppress
rhm1
defects by diverting rhamnose to the synthesis of cell wall polysaccharides.
Therefore, rhamnose is required in the cell wall for normal expansion of cotyledon epidermal cells.
Our findings suggest a broad role for rhamnose-containing cell wall polysaccharides in the morphogenesis of epidermal cells.
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