Regulation and function of a polarly localized lignin barrier in the exodermis

Concepcion Manzano*, Kevin W. Morimoto, Lidor Shaar-Moshe, G. Alex Mason, Alex Cantó-Pastor, Mona Gouran, Damien De Bellis, Robertas Ursache, Kaisa Kajala, Neelima Sinha, Julia Bailey-Serres, Niko Geldner, J. Carlos del Pozo, Siobhan M. Brady*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Multicellular organisms control environmental interactions through specialized barriers in specific cell types. A conserved barrier in plant roots is the endodermal Casparian strip (CS), a ring-like structure made of polymerized lignin that seals the endodermal apoplastic space. Most angiosperms have another root cell type, the exodermis, that is reported to form a barrier. Our understanding of exodermal developmental and molecular regulation and function is limited as this cell type is absent from Arabidopsis thaliana. We demonstrate that in tomato (Solanum lycopersicum), the exodermis does not form a CS. Instead, it forms a polar lignin cap (PLC) with equivalent barrier function to the endodermal CS but distinct genetic control. Repression of the exodermal PLC in inner cortical layers is conferred by the SlSCZ and SlEXO1 transcription factors, and these two factors genetically interact to control its polar deposition. Several target genes that act downstream of SlSCZ and SlEXO1 in the exodermis are identified. Although the exodermis and endodermis produce barriers that restrict mineral ion uptake, the exodermal PLC is unable to fully compensate for the lack of a CS. The presence of distinct lignin structures acting as apoplastic barriers has exciting implications for a root’s response to abiotic and biotic stimuli.

Original languageEnglish
Article number2320
Pages (from-to)118–130
Number of pages13
JournalNature Plants
Volume11
Issue number1
Early online date2 Dec 2024
DOIs
Publication statusPublished - 2025

Bibliographical note

Publisher Copyright:
© The Author(s) 2024.

Funding

We thank A. M. Bagman for experimental assistance; P. A. Merlos de Santa Ana for insightful comments on the project and manuscript. Funding was as follows: MSCA GF 655406 to C.M.; NSF 2118017 to K.W.M., C.M. and S.M.B.; NSF PGRP IOS-1856749 and IOS-211980 to S.M.B., A.C.-P., J.B.-S. and N.S.; BARD FI-570-2018, HFSP #RGP0067 and Postdoctoral Career Development Award in Science to L.S.-M.; NSF PRFB IOS-1907008 to G.A.M.; EMBO Long-term Fellowship ALTF 1046-2015 to R.U.; SKR Postdoctoral Fellowship and MSCA RI Fellowship 790057 to K.K.; BIO2017-82209-R to J.C.d.P.; HHMI 55108506 to M.G. and S.M.B.

FundersFunder number
Howard Hughes Medical Institute (HHMI)PRFB IOS-1907008
NSFPGRP IOS-1856749, IOS-211980
HFSPRGP0067
Postdoctoral Career Development Award in Science
EMBO Long-term FellowshipALTF 1046-2015
MSCA RI Fellowship790057, BIO2017-82209-R, HHMI 55108506

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