Hsp70 plays a role in programmed cell death during the remodelling of leaves of the lace plant (Aponogeton madagascariensis)

Nathan M. Rowarth, Adrian N. Dauphinee, Georgia L. Denbigh, Arunika Hlan Gunawardena

Research output: Contribution to journalArticlepeer-review

31 Citations (Scopus)

Abstract

Lace plant leaves utilize programmed cell death (PCD) to form perforations during development. The role of heat shock proteins (Hsps) in PCD during lace plant leaf development is currently unknown. Hsp70 amounts were measured throughout lace plant leaf development, and the results indicate that it is highest before and during PCD. Increased Hsp70 amounts correlate with raised anthocyanin content and caspase-like protease (CLP) activity. To investigate the effects of Hsp70 on leaf development, whole plants were treated with either of the known regulators of PCD [reactive oxygen species (ROS) or antioxidants] or an Hsp70 inhibitor, chlorophenylethynylsulfonamide (PES-Cl). ROS treatment significantly increased Hsp70 2-fold and CLP activity in early developing leaves, but no change in anthocyanin and the number of perforations formed was observed. Antioxidant treatment significantly decreased Hsp70, anthocyanin, and CLP activity in early leaves, resulting in the fewest perforations. PES-Cl (25 μM) treatment significantly increased Hsp70 4-fold in early leaves, while anthocyanin, superoxide, and CLP activity significantly declined, leading to fewer perforations. Results show that significantly increased (4-fold) or decreased Hsp70 amounts lead to lower anthocyanin and CLP activity, inhibiting PCD induction. Our data support the hypothesis that Hsp70 plays a role in regulating PCD at a threshold in lace plant leaf development. Hsp70 affects anthocyanin content and caspase-like protease activity, and helps regulate PCD during the remodelling of leaves of lace plant, Aponogeton madagascariensis.

Original languageEnglish
Pages (from-to)907-918
Number of pages12
JournalJournal of Experimental Botany
Volume71
Issue number3
DOIs
Publication statusPublished - Jan 23 2020

Bibliographical note

Funding Information:
We thank the Brent Johnston lab (Dalhousie University) for the use of their fluorometer. We also thank Dr Christian Lacroix (University of Prince Edward Island) and Michaela Kember (Dalhousie University) for critically reviewing the manuscript. Funding was supported by AHLANG’s Natural Science and Engineering Research Council of Canada (NSERC) Discovery (#2017-04299) and Discovery Accelerator Supplements (DAS, 2017-507825). AND was funded by AHLANG’s NSERC DAS. Thanks to NSERC post-graduate scholarships and a Nova Scotia Graduate Scholarship for graduate student funding to NMR and GLD.

Publisher Copyright:
© 2019 The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Experimental Biology.

ASJC Scopus Subject Areas

  • Physiology
  • Plant Science

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