Transcriptome analyses of leaf architecture in Sansevieria support a common genetic toolkit in the parallel evolution of unifacial leaves in monocots

Abstract Planar structures dramatically increase the surface‐area‐to‐volume ratio, which is critically important for multicellular organisms. In this study, we utilize naturally occurring phenotypic variation among three Sansivieria species (Asperagaceae) to investigate leaf margin expression patter...

Full description

Bibliographic Details
Main Authors: Edward M. Golenberg, Aleksandar Popadić, Weilong Hao
Format: Article
Language:English
Published: Wiley 2023-08-01
Series:Plant Direct
Subjects:
Online Access:https://doi.org/10.1002/pld3.511
_version_ 1797734959022080000
author Edward M. Golenberg
Aleksandar Popadić
Weilong Hao
author_facet Edward M. Golenberg
Aleksandar Popadić
Weilong Hao
author_sort Edward M. Golenberg
collection DOAJ
description Abstract Planar structures dramatically increase the surface‐area‐to‐volume ratio, which is critically important for multicellular organisms. In this study, we utilize naturally occurring phenotypic variation among three Sansivieria species (Asperagaceae) to investigate leaf margin expression patterns that are associated with mediolateral and adaxial/abaxial development. We identified differentially expressed genes (DEGs) between center and margin leaf tissues in two planar‐leaf species Sansevieria subspicata and Sansevieria trifasciata and compared these with expression patterns within the cylindrically leaved Sansevieria cylindrica. Two YABBY family genes, homologs of FILAMENTOUS FLOWER and DROOPING LEAF, are overexpressed in the center leaf tissue in the planar‐leaf species and in the tissue of the cylindrical leaves. As mesophyll structure does not indicate adaxial versus abaxial differentiation, increased leaf thickness results in more water‐storage tissue and enhances resistance to aridity. This suggests that the cylindrical‐leaf in S. cylindrica is analogous to the central leaf tissue in the planar‐leaf species. Furthermore, the congruence of the expression patterns of these YABBY genes in Sansevieria with expression patterns found in other unifacial monocot species suggests that patterns of parallel evolution may be the result of similar solutions derived from a limited developmental toolbox.
first_indexed 2024-03-12T12:51:27Z
format Article
id doaj.art-e7a4aac1fd9849ed9cccfb96294461bd
institution Directory Open Access Journal
issn 2475-4455
language English
last_indexed 2024-03-12T12:51:27Z
publishDate 2023-08-01
publisher Wiley
record_format Article
series Plant Direct
spelling doaj.art-e7a4aac1fd9849ed9cccfb96294461bd2023-08-28T22:42:32ZengWileyPlant Direct2475-44552023-08-0178n/an/a10.1002/pld3.511Transcriptome analyses of leaf architecture in Sansevieria support a common genetic toolkit in the parallel evolution of unifacial leaves in monocotsEdward M. Golenberg0Aleksandar Popadić1Weilong Hao2Department of Biological Sciences Wayne State University Detroit Michigan USADepartment of Biological Sciences Wayne State University Detroit Michigan USADepartment of Biological Sciences Wayne State University Detroit Michigan USAAbstract Planar structures dramatically increase the surface‐area‐to‐volume ratio, which is critically important for multicellular organisms. In this study, we utilize naturally occurring phenotypic variation among three Sansivieria species (Asperagaceae) to investigate leaf margin expression patterns that are associated with mediolateral and adaxial/abaxial development. We identified differentially expressed genes (DEGs) between center and margin leaf tissues in two planar‐leaf species Sansevieria subspicata and Sansevieria trifasciata and compared these with expression patterns within the cylindrically leaved Sansevieria cylindrica. Two YABBY family genes, homologs of FILAMENTOUS FLOWER and DROOPING LEAF, are overexpressed in the center leaf tissue in the planar‐leaf species and in the tissue of the cylindrical leaves. As mesophyll structure does not indicate adaxial versus abaxial differentiation, increased leaf thickness results in more water‐storage tissue and enhances resistance to aridity. This suggests that the cylindrical‐leaf in S. cylindrica is analogous to the central leaf tissue in the planar‐leaf species. Furthermore, the congruence of the expression patterns of these YABBY genes in Sansevieria with expression patterns found in other unifacial monocot species suggests that patterns of parallel evolution may be the result of similar solutions derived from a limited developmental toolbox.https://doi.org/10.1002/pld3.511abaxialadaxialcylindrical leafdevelopmentdifferential gene expressionflat leaf
spellingShingle Edward M. Golenberg
Aleksandar Popadić
Weilong Hao
Transcriptome analyses of leaf architecture in Sansevieria support a common genetic toolkit in the parallel evolution of unifacial leaves in monocots
Plant Direct
abaxial
adaxial
cylindrical leaf
development
differential gene expression
flat leaf
title Transcriptome analyses of leaf architecture in Sansevieria support a common genetic toolkit in the parallel evolution of unifacial leaves in monocots
title_full Transcriptome analyses of leaf architecture in Sansevieria support a common genetic toolkit in the parallel evolution of unifacial leaves in monocots
title_fullStr Transcriptome analyses of leaf architecture in Sansevieria support a common genetic toolkit in the parallel evolution of unifacial leaves in monocots
title_full_unstemmed Transcriptome analyses of leaf architecture in Sansevieria support a common genetic toolkit in the parallel evolution of unifacial leaves in monocots
title_short Transcriptome analyses of leaf architecture in Sansevieria support a common genetic toolkit in the parallel evolution of unifacial leaves in monocots
title_sort transcriptome analyses of leaf architecture in sansevieria support a common genetic toolkit in the parallel evolution of unifacial leaves in monocots
topic abaxial
adaxial
cylindrical leaf
development
differential gene expression
flat leaf
url https://doi.org/10.1002/pld3.511
work_keys_str_mv AT edwardmgolenberg transcriptomeanalysesofleafarchitectureinsansevieriasupportacommongenetictoolkitintheparallelevolutionofunifacialleavesinmonocots
AT aleksandarpopadic transcriptomeanalysesofleafarchitectureinsansevieriasupportacommongenetictoolkitintheparallelevolutionofunifacialleavesinmonocots
AT weilonghao transcriptomeanalysesofleafarchitectureinsansevieriasupportacommongenetictoolkitintheparallelevolutionofunifacialleavesinmonocots