Differentially expressed chaperone genes reveal a stress response required for unidirectional regeneration in the basal chordate Ciona

BMC Biology

Research Article

Mandy Ng¹  Li Ma²  William R. Jeffery³  Lianwei Li⁴  Bo Li⁵  Špela Gorički⁶ 

[1]Department of Biology, University of Maryland, 20742, College Park, MD, USA

[2]Department of Biology, University of Maryland, 20742, College Park, MD, USA

[3]Marine Biological Laboratory, 02543, Woods Hole, MA, USA

[4]Kunming Institute of Zoology, Chinese Academy of Sciences, 650223, Kunming, China

[5]Department of Biology, University of Maryland, 20742, College Park, MD, USA

[6]Marine Biological Laboratory, 02543, Woods Hole, MA, USA

[7]Station Biologique, 29680, Roscoff, France

[8]Kunming Institute of Zoology, Chinese Academy of Sciences, 650223, Kunming, China

[9]Kunming Institute of Zoology, Chinese Academy of Sciences, 650223, Kunming, China

[10]Kunming College of Life Science, University of Chinese Academy of Sciences, 100049, Beijing, China

[11]Station Biologique, 29680, Roscoff, France

[12]Scriptorium Biologorum, 9000, Murska Sobota, Slovenia

关键词: Ciona intestinalis;    Basal chordate;    Branchial sac transcriptome;    Regeneration;    Stress response;    HSP70 chaperone system;   

DOI  :  10.1186/s12915-023-01633-y

 received in 2023-01-20, accepted in 2023-05-25,  发布年份 2023

来源: Springer

【 摘 要 】

BackgroundUnidirectional regeneration in the basal chordate Ciona intestinalis involves the proliferation of adult stem cells residing in the branchial sac vasculature and the migration of progenitor cells to the site of distal injury. However, after the Ciona body is bisected, regeneration occurs in the proximal but not in the distal fragments, even if the latter include a part of the branchial sac with stem cells. A transcriptome was sequenced and assembled from the isolated branchial sacs of regenerating animals, and the information was used to provide insights into the absence of regeneration in distal body fragments.ResultsWe identified 1149 differentially expressed genes, which were separated into two major modules by weighted gene correlation network analysis, one consisting of mostly upregulated genes correlated with regeneration and the other consisting of only downregulated genes associated with metabolism and homeostatic processes. The hsp70, dnaJb4, and bag3 genes were among the highest upregulated genes and were predicted to interact in an HSP70 chaperone system. The upregulation of HSP70 chaperone genes was verified and their expression confirmed in BS vasculature cells previously identified as stem and progenitor cells. siRNA-mediated gene knockdown showed that hsp70 and dnaJb4, but not bag3, are required for progenitor cell targeting and distal regeneration. However, neither hsp70 nor dnaJb4 were strongly expressed in the branchial sac vasculature of distal fragments, implying the absence of a stress response. Heat shock treatment of distal body fragments activated hsp70 and dnaJb4 expression indicative of a stress response, induced cell proliferation in branchial sac vasculature cells, and promoted distal regeneration.ConclusionsThe chaperone system genes hsp70, dnaJb4, and bag3 are significantly upregulated in the branchial sac vasculature following distal injury, defining a stress response that is essential for regeneration. The stress response is absent from distal fragments, but can be induced by a heat shock, which activates cell division in the branchial sac vasculature and promotes distal regeneration. This study demonstrates the importance of a stress response for stem cell activation and regeneration in a basal chordate, which may have implications for understanding the limited regenerative activities in other animals, including vertebrates.

【 授权许可】

CC BY   
© The Author(s) 2023

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