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Tracheophytes Contain Conserved Orthologs of a Basic Helix-Loop-Helix Transcription Factor That Modulate ROOT HAIR SPECIFIC Genes.

Identifieur interne : 001145 ( Main/Exploration ); précédent : 001144; suivant : 001146

Tracheophytes Contain Conserved Orthologs of a Basic Helix-Loop-Helix Transcription Factor That Modulate ROOT HAIR SPECIFIC Genes.

Auteurs : Youra Hwang [Corée du Sud] ; Hee-Seung Choi [Corée du Sud] ; Hyun-Min Cho [Corée du Sud] ; Hyung-Taeg Cho [Corée du Sud]

Source :

RBID : pubmed:28087829

Descripteurs français

English descriptors

Abstract

ROOT HAIR SPECIFIC (RHS) genes, which contain the root hair-specific cis-element (RHE) in their regulatory regions, function in root hair morphogenesis. Here, we demonstrate that an Arabidopsis thaliana basic helix-loop-helix transcription factor, ROOT HAIR DEFECTVE SIX-LIKE4 (RSL4), directly binds to the RHE in vitro and in vivo, upregulates RHS genes, and stimulates root hair formation in Arabidopsis. Orthologs of RSL4 from a eudicot (poplar [Populus trichocarpa]), a monocot (rice [Oryza sativa]), and a lycophyte (Selaginella moellendorffii) each restored root hair growth in the Arabidopsis rsl4 mutant. In addition, the rice and S. moellendorffii RSL4 orthologs bound to the RHE in in vitro and in vivo assays. The RSL4 orthologous genes contain RHEs in their promoter regions, and RSL4 was able to bind to its own RHEs in vivo and amplify its own expression. This process likely provides a positive feedback loop for sustainable root hair growth. When RSL4 and its orthologs were expressed in cells in non-root-hair positions, they induced ectopic root hair growth, indicating that these genes are sufficient to specify root hair formation. Our results suggest that RSL4 mediates root hair formation by regulating RHS genes and that this mechanism is conserved throughout the tracheophyte (vascular plant) lineage.

DOI: 10.1105/tpc.16.00732
PubMed: 28087829
PubMed Central: PMC5304353


Affiliations:


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<term>Arabidopsis Proteins (genetics)</term>
<term>Arabidopsis Proteins (metabolism)</term>
<term>Base Sequence (MeSH)</term>
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<term>Basic Helix-Loop-Helix Transcription Factors (genetics)</term>
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<term>Microscopy, Confocal (MeSH)</term>
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<term>Oryza (metabolism)</term>
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<term>Arabidopsis (métabolisme)</term>
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<term>Protéines d'Arabidopsis (métabolisme)</term>
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<div type="abstract" xml:lang="en">
<i>ROOT HAIR SPECIFIC</i>
(
<i>RHS</i>
) genes, which contain the root hair-specific
<i>cis</i>
-element (RHE) in their regulatory regions, function in root hair morphogenesis. Here, we demonstrate that an
<i>Arabidopsis thaliana</i>
basic helix-loop-helix transcription factor, ROOT HAIR DEFECTVE SIX-LIKE4 (RSL4), directly binds to the RHE in vitro and in vivo, upregulates
<i>RHS</i>
genes, and stimulates root hair formation in Arabidopsis. Orthologs of RSL4 from a eudicot (poplar [
<i>Populus trichocarpa</i>
]), a monocot (rice [
<i>Oryza sativa</i>
]), and a lycophyte (
<i>Selaginella moellendorffii</i>
) each restored root hair growth in the Arabidopsis
<i>rsl4</i>
mutant. In addition, the rice and
<i>S. moellendorffii</i>
RSL4 orthologs bound to the RHE in in vitro and in vivo assays. The
<i>RSL4</i>
orthologous genes contain RHEs in their promoter regions, and RSL4 was able to bind to its own RHEs in vivo and amplify its own expression. This process likely provides a positive feedback loop for sustainable root hair growth. When
<i>RSL4</i>
and its orthologs were expressed in cells in non-root-hair positions, they induced ectopic root hair growth, indicating that these genes are sufficient to specify root hair formation. Our results suggest that RSL4 mediates root hair formation by regulating
<i>RHS</i>
genes and that this mechanism is conserved throughout the tracheophyte (vascular plant) lineage.</div>
</front>
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<i>ROOT HAIR SPECIFIC</i>
(
<i>RHS</i>
) genes, which contain the root hair-specific
<i>cis</i>
-element (RHE) in their regulatory regions, function in root hair morphogenesis. Here, we demonstrate that an
<i>Arabidopsis thaliana</i>
basic helix-loop-helix transcription factor, ROOT HAIR DEFECTVE SIX-LIKE4 (RSL4), directly binds to the RHE in vitro and in vivo, upregulates
<i>RHS</i>
genes, and stimulates root hair formation in Arabidopsis. Orthologs of RSL4 from a eudicot (poplar [
<i>Populus trichocarpa</i>
]), a monocot (rice [
<i>Oryza sativa</i>
]), and a lycophyte (
<i>Selaginella moellendorffii</i>
) each restored root hair growth in the Arabidopsis
<i>rsl4</i>
mutant. In addition, the rice and
<i>S. moellendorffii</i>
RSL4 orthologs bound to the RHE in in vitro and in vivo assays. The
<i>RSL4</i>
orthologous genes contain RHEs in their promoter regions, and RSL4 was able to bind to its own RHEs in vivo and amplify its own expression. This process likely provides a positive feedback loop for sustainable root hair growth. When
<i>RSL4</i>
and its orthologs were expressed in cells in non-root-hair positions, they induced ectopic root hair growth, indicating that these genes are sufficient to specify root hair formation. Our results suggest that RSL4 mediates root hair formation by regulating
<i>RHS</i>
genes and that this mechanism is conserved throughout the tracheophyte (vascular plant) lineage.</AbstractText>
<CopyrightInformation>© 2017 American Society of Plant Biologists. All rights reserved.</CopyrightInformation>
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<QualifierName UI="Q000145" MajorTopicYN="N">classification</QualifierName>
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</MeshHeading>
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</MeshHeading>
<MeshHeading>
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</MeshHeading>
<MeshHeading>
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