Differential Recruitment of WOX Transcription Factors for Lateral Development and Organ Fusion in Petunia and Arabidopsis

Petal fusion in petunia (Petunia x hybrida) results from lateral expansion of the five initially separate petal primordia, forming a ring-like primordium that determines further development. Here, we show that MAEWEST (MAW) and CHORIPETALA SUZANNE (CHSU) are required for petal and carpel fusion, as...

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Published in	The Plant cell Vol. 21; no. 8; pp. 2269 - 2283
Main Authors	Vandenbussche, Michiel, Horstman, Anneke, Zethof, Jan, Koes, Ronald, Rijpkema, Anneke S, Gerats, Tom
Format	Journal Article
Language	English
Published	United States American Society of Plant Biologists 01.08.2009
Subjects	Alleles Amino Acid Sequence Arabidopsis Arabidopsis - genetics Arabidopsis - growth & development Arabidopsis - metabolism Arabidopsis - ultrastructure Arabidopsis Proteins Arabidopsis Proteins - chemistry Arabidopsis Proteins - genetics Arabidopsis Proteins - metabolism Arabidopsis thaliana Carpels chemistry corolla Cryoelectron Microscopy Flowers Flowers - genetics Flowers - growth & development Flowers - metabolism Flowers - ultrastructure Genes genetics growth & development In Situ Hybridization Leaf blade Leaves metabolism Molecular Sequence Data mutants Petals Petunia Petunia - genetics Petunia - growth & development Petunia - metabolism Petunia - ultrastructure Petunia hybrida Phenotypes Phylogeny Plant cells Plant Leaves Plant Leaves - genetics Plant Leaves - growth & development Plant Leaves - metabolism Plant Leaves - ultrastructure Plant Proteins Plant Proteins - chemistry Plant Proteins - genetics Plant Proteins - metabolism Plants Reverse Transcriptase Polymerase Chain Reaction transcription factors Transcription Factors - chemistry Transcription Factors - genetics Transcription Factors - metabolism Transposons ultrastructure
Online Access	Get full text
ISSN	1040-4651 1532-298X
DOI	10.1105/tpc.109.065862

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Abstract	Petal fusion in petunia (Petunia x hybrida) results from lateral expansion of the five initially separate petal primordia, forming a ring-like primordium that determines further development. Here, we show that MAEWEST (MAW) and CHORIPETALA SUZANNE (CHSU) are required for petal and carpel fusion, as well as for lateral outgrowth of the leaf blade. Morphological and molecular analysis of maw and maw chsu double mutants suggest that polarity defects along the adaxial/abaxial axis contribute to the observed reduced lateral outgrowth of organ primordia. We show that MAW encodes a member of the WOX (WUSCHEL-related homeobox) transcription factor family and that a partly similar function is redundantly encoded by WOX1 and PRESSED FLOWER (PRS) in Arabidopsis thaliana, indicating a conserved role for MAW/WOX1/PRS genes in regulating lateral organ development. Comparison of petunia maw and Arabidopsis wox1 prs phenotypes suggests differential recruitment of WOX gene function depending on organ type and species. Our comparative data together with previous reports on WOX gene function in different species identify the WOX gene family as highly dynamic and, therefore, an attractive subject for future evo-devo studies.
AbstractList	Petal fusion in petunia (Petunia x hybrida) results from lateral expansion of the five initially separate petal primordia, forming a ring-like primordium that determines further development. Here, we show that MAEWEST (MAW) and CHORIPETALA SUZANNE (CHSU) are required for petal and carpel fusion, as well as for lateral outgrowth of the leaf blade. Morphological and molecular analysis of maw and maw chsu double mutants suggest that polarity defects along the adaxial/abaxial axis contribute to the observed reduced lateral outgrowth of organ primordia. We show that MAW encodes a member of the WOX (WUSCHEL-related homeobox) transcription factor family and that a partly similar function is redundantly encoded by WOX1 and PRESSED FLOWER (PRS) in Arabidopsis thaliana, indicating a conserved role for MAW/WOX1/PRS genes in regulating lateral organ development. Comparison of petunia maw and Arabidopsis wox1 prs phenotypes suggests differential recruitment of WOX gene function depending on organ type and species. Our comparative data together with previous reports on WOX gene function in different species identify the WOX gene family as highly dynamic and, therefore, an attractive subject for future evo-devo studies. Petal fusion in petunia (Petunia × hybrida) results from lateral expansion of the five initially separate petal primordia, forming a ring-like primordium that determines further development. Here, we show that MAEWEST (MAW) and CHORIPETALA SUZANNE (CHSU) are required for petal and carpel fusion, as well as for lateral outgrowth of the leaf blade. Morphological and molecular analysis of maw and maw chsu double mutants suggest that polarity defects along the adaxial/abaxial axis contribute to the observed reduced lateral outgrowth of organ primordia. We show that MAW encodes a member of the WOX (WUSCHEL-reiaXed homeobox) transcription factor family and that a partly similar function is redundantly encoded by WOX1 and PRESSED FLOWER (PRS) in Arabidopsis thaliana, indicating a conserved role for MAW/WOX1/PRS genes in regulating lateral organ development. Comparison of petunia maw and Arabidopsis wox1 prs phenotypes suggests differential recruitment of WOX gene function depending on organ type and species. Our comparative data together with previous reports on WOX gene function in different species identify the WOX gene family as highly dynamic and, therefore, an attractive subject for future evo-devo studies. Petal fusion in petunia (Petunia × hybrida) results from lateral expansion of the five initially separate petal primordia, forming a ring-like primordium that determines further development. Here, we show that MAEWEST (MAW) and CHORIPETALA SUZANNE (CHSU) are required for petal and carpel fusion, as well as for lateral outgrowth of the leaf blade. Morphological and molecular analysis of maw and maw chsu double mutants suggest that polarity defects along the adaxial/abaxial axis contribute to the observed reduced lateral outgrowth of organ primordia. We show that MAW encodes a member of the WOX (WUSCHEL-related homeobox) transcription factor family and that a partly similar function is redundantly encoded by WOX1 and PRESSED FLOWER (PRS) in Arabidopsis thaliana, indicating a conserved role for MAW/WOX1/PRS genes in regulating lateral organ development. Comparison of petunia maw and Arabidopsis wox1 prs phenotypes suggests differential recruitment of WOX gene function depending on organ type and species. Our comparative data together with previous reports on WOX gene function in different species identify the WOX gene family as highly dynamic and, therefore, an attractive subject for future evo-devo studies. Petal fusion in petunia (Petunia x hybrida) results from lateral expansion of the five initially separate petal primordia, forming a ring-like primordium that determines further development. Here, we show that MAEWEST (MAW) and CHORIPETALA SUZANNE (CHSU) are required for petal and carpel fusion, as well as for lateral outgrowth of the leaf blade. Morphological and molecular analysis of maw and maw chsu double mutants suggest that polarity defects along the adaxial/abaxial axis contribute to the observed reduced lateral outgrowth of organ primordia. We show that MAW encodes a member of the WOX (WUSCHEL-related homeobox) transcription factor family and that a partly similar function is redundantly encoded by WOX1 and PRESSED FLOWER (PRS) in Arabidopsis thaliana, indicating a conserved role for MAW/WOX1/PRS genes in regulating lateral organ development. Comparison of petunia maw and Arabidopsis wox1 prs phenotypes suggests differential recruitment of WOX gene function depending on organ type and species. Our comparative data together with previous reports on WOX gene function in different species identify the WOX gene family as highly dynamic and, therefore, an attractive subject for future evo-devo studies.Petal fusion in petunia (Petunia x hybrida) results from lateral expansion of the five initially separate petal primordia, forming a ring-like primordium that determines further development. Here, we show that MAEWEST (MAW) and CHORIPETALA SUZANNE (CHSU) are required for petal and carpel fusion, as well as for lateral outgrowth of the leaf blade. Morphological and molecular analysis of maw and maw chsu double mutants suggest that polarity defects along the adaxial/abaxial axis contribute to the observed reduced lateral outgrowth of organ primordia. We show that MAW encodes a member of the WOX (WUSCHEL-related homeobox) transcription factor family and that a partly similar function is redundantly encoded by WOX1 and PRESSED FLOWER (PRS) in Arabidopsis thaliana, indicating a conserved role for MAW/WOX1/PRS genes in regulating lateral organ development. Comparison of petunia maw and Arabidopsis wox1 prs phenotypes suggests differential recruitment of WOX gene function depending on organ type and species. Our comparative data together with previous reports on WOX gene function in different species identify the WOX gene family as highly dynamic and, therefore, an attractive subject for future evo-devo studies. Petal fusion in petunia ( Petunia × hybrida ) results from lateral expansion of the five initially separate petal primordia, forming a ring-like primordium that determines further development. Here, we show that MAEWEST ( MAW ) and CHORIPETALA SUZANNE ( CHSU ) are required for petal and carpel fusion, as well as for lateral outgrowth of the leaf blade. Morphological and molecular analysis of maw and maw chsu double mutants suggest that polarity defects along the adaxial/abaxial axis contribute to the observed reduced lateral outgrowth of organ primordia. We show that MAW encodes a member of the WOX ( WUSCHEL -related homeobox) transcription factor family and that a partly similar function is redundantly encoded by WOX1 and PRESSED FLOWER ( PRS ) in Arabidopsis thaliana , indicating a conserved role for MAW / WOX1 / PRS genes in regulating lateral organ development. Comparison of petunia maw and Arabidopsis wox1 prs phenotypes suggests differential recruitment of WOX gene function depending on organ type and species. Our comparative data together with previous reports on WOX gene function in different species identify the WOX gene family as highly dynamic and, therefore, an attractive subject for future evo-devo studies.
Author	Vandenbussche, Michiel Rijpkema, Anneke S Koes, Ronald Horstman, Anneke Gerats, Tom Zethof, Jan
AuthorAffiliation	a Department of Plant Genetics, Institute for Water and Wetland Research, Radboud University Nijmegen, 6525 ED, Nijmegen, The Netherlands b Department of Genetics, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands
AuthorAffiliation_xml	– name: b Department of Genetics, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands – name: a Department of Plant Genetics, Institute for Water and Wetland Research, Radboud University Nijmegen, 6525 ED, Nijmegen, The Netherlands
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BackLink	https://www.ncbi.nlm.nih.gov/pubmed/19717616$$D View this record in MEDLINE/PubMed
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ContentType	Journal Article
Copyright	Copyright 2009 American Society of Plant Biologists Copyright American Society of Plant Biologists Aug 2009 Copyright © 2009, American Society of Plant Biologists
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Notes	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 www.plantcell.org/cgi/doi/10.1105/tpc.109.065862 Online version contains Web-only data. Address correspondence to m.vandenbussche@science.ru.nl. The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantcell.org) is: Michiel Vandenbussche (m.vandenbussche@science.ru.nl).
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Snippet	Petal fusion in petunia (Petunia x hybrida) results from lateral expansion of the five initially separate petal primordia, forming a ring-like primordium that... Petal fusion in petunia (Petunia × hybrida) results from lateral expansion of the five initially separate petal primordia, forming a ring-like primordium that... Petal fusion in petunia ( Petunia × hybrida ) results from lateral expansion of the five initially separate petal primordia, forming a ring-like primordium...
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StartPage	2269
SubjectTerms	Alleles Amino Acid Sequence Arabidopsis Arabidopsis - genetics Arabidopsis - growth & development Arabidopsis - metabolism Arabidopsis - ultrastructure Arabidopsis Proteins Arabidopsis Proteins - chemistry Arabidopsis Proteins - genetics Arabidopsis Proteins - metabolism Arabidopsis thaliana Carpels chemistry corolla Cryoelectron Microscopy Flowers Flowers - genetics Flowers - growth & development Flowers - metabolism Flowers - ultrastructure Genes genetics growth & development In Situ Hybridization Leaf blade Leaves metabolism Molecular Sequence Data mutants Petals Petunia Petunia - genetics Petunia - growth & development Petunia - metabolism Petunia - ultrastructure Petunia hybrida Phenotypes Phylogeny Plant cells Plant Leaves Plant Leaves - genetics Plant Leaves - growth & development Plant Leaves - metabolism Plant Leaves - ultrastructure Plant Proteins Plant Proteins - chemistry Plant Proteins - genetics Plant Proteins - metabolism Plants Reverse Transcriptase Polymerase Chain Reaction transcription factors Transcription Factors - chemistry Transcription Factors - genetics Transcription Factors - metabolism Transposons ultrastructure
Title	Differential Recruitment of WOX Transcription Factors for Lateral Development and Organ Fusion in Petunia and Arabidopsis
URI	https://www.jstor.org/stable/40537000 https://www.ncbi.nlm.nih.gov/pubmed/19717616 https://www.proquest.com/docview/218785359 https://www.proquest.com/docview/46409054 https://www.proquest.com/docview/734074518 https://pubmed.ncbi.nlm.nih.gov/PMC2751957
Volume	21
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