Skip to main content
Log in

Regulation of the unfolded protein response during dehydration stress in African clawed frogs, Xenopus laevis

  • Original Article
  • Published:
Cell Stress and Chaperones Aims and scope

Abstract

The unfolded protein response (UPR) is a wide-ranging cellular response to accumulation of malfolded proteins in the endoplasmic reticulum (ER) and acts as a quality control mechanism to halt protein processing and repair/destroy malfolded proteins under stress conditions of many kinds. Among vertebrate species, amphibians experience the greatest challenges in maintaining water and osmotic balance, the high permeability of their skin making them very susceptible to dehydration and challenging their ability to maintain cellular homeostasis. The present study evaluates the involvement of the UPR in dealing with dehydration-mediated disruption of protein processing in the tissues of African clawed frogs, Xenopus laevis. This primarily aquatic frog must deal with seasonal drought conditions in its native southern Africa environment. Key markers of cellular stress that impact protein processing were identified in six tissues of frogs that had lost 28% of total body water, as compared with fully hydrated controls. This included upregulation of glucose-regulated proteins (GRPs) that are resident chaperones in the ER, particularly 2–ninefold increases in GRP58, GRP75, and/or GRP94 in the lung and skin. Activating transcription factors (ATF3, ATF4, ATF6) that mediate UPR responses also responded to dehydration stress, particularly in skeletal muscle where both ATF3 and ATF4 rose strongly in the nucleus. Other protein markers of the UPR including GADD34, GADD153, EDEM, and XBP-1 also showed selective upregulation in frog tissues in response to dehydration and nuclear levels of the transcription factors XBP-1 and P-CREB rose indicating up-regulation of genes under their control.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

Abbreviations

ATF:

Activating transcription factor

CREB:

cAMP response element-binding protein

EDEM:

ER degradation-enhancing alpha-mannosidase-like 1

eIF2α:

Eukaryotic initiation factor 2α

ER:

Endoplasmic reticulum

ERAD:

ER-associated degradation

ERK:

Extracellular signal-regulated kinase

FoxO:

Forkhead box transcription factor, subgroup O

GAAD:

Growth arrest and DNA damage protein

GRP:

Glucose-regulated protein

HSP:

Heat shock protein

IRE1:

Inositol-requiring kinase 1

PDI:

Protein disulfide isomerase

PERK:

PKR-like eukaryotic initiation factor 2α kinase

SDS-PAGE:

Sodium dodecyl-sulfate polyacrylamide gel electrophoresis

UPR:

Unfolded protein response

XBP1:

X-box binding protein 1

References

Download references

Acknowledgements

This research was supported by a Discovery grant from the Natural Sciences and Engineering Research Council of Canada to KBS (#6793); KBS holds the Canada Research Chair in Molecular Physiology.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Kenneth B. Storey.

Ethics declarations

Conflict of interest

The authors declare that they have no financial or non-financial interests that are directly or indirectly related to the work submitted for publication.

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Malik, A.I., Storey, J.M. & Storey, K.B. Regulation of the unfolded protein response during dehydration stress in African clawed frogs, Xenopus laevis. Cell Stress and Chaperones 28, 529–540 (2023). https://doi.org/10.1007/s12192-022-01275-z

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12192-022-01275-z

Keywords

Navigation