Evolutionary diversification reveals distinct somatic versus germline cytoskeletal functions of the Arp2 branched actin nucleator protein.

Arp2 Drosophila actin cytoskeleton evolution fertility germline individualization paralogs sperm development

Journal

Current biology : CB
ISSN: 1879-0445
Titre abrégé: Curr Biol
Pays: England
ID NLM: 9107782

Informations de publication

Date de publication:
09 Nov 2023
Historique:
received: 03 04 2023
revised: 18 09 2023
accepted: 25 10 2023
medline: 18 11 2023
pubmed: 18 11 2023
entrez: 17 11 2023
Statut: aheadofprint

Résumé

Branched actin networks are critical in many cellular processes, including cell motility and division. Arp2, a protein within the seven-membered Arp2/3 complex, is responsible for generating branched actin. Given its essential roles, Arp2 evolves under stringent sequence conservation throughout eukaryotic evolution. We unexpectedly discovered recurrent evolutionary diversification of Arp2 in Drosophila, yielding independently arising paralogs Arp2D in obscura species and Arp2D2 in montium species. Both paralogs are unusually testis-enriched in expression relative to Arp2. We investigated whether their sequence divergence from canonical Arp2 led to functional specialization by replacing Arp2 in D. melanogaster with either Arp2D or Arp2D2. Despite their divergence, we surprisingly found that both complement Arp2's essential function in somatic tissue, suggesting they have preserved the ability to polymerize branched actin even in a non-native species. However, we found that Arp2D- and Arp2D2-expressing males display defects throughout sperm development, with Arp2D resulting in more pronounced deficiencies and subfertility, suggesting the Arp2 paralogs are cross-species incompatible in the testis. We focused on Arp2D and pinpointed two highly diverged structural regions-the D-loop and C terminus-and found that they contribute to germline defects in D. melanogaster sperm development. However, while the Arp2D C terminus is suboptimal in the D. melanogaster testis, it is essential for Arp2D somatic function. Testis cytology of the paralogs' native species revealed striking differences in germline actin structures, indicating unique cytoskeletal requirements. Our findings suggest canonical Arp2 function differs between somatic versus germline contexts, and Arp2 paralogs may have recurrently evolved for species-specialized actin branching in the testis.

Identifiants

pubmed: 37977138
pii: S0960-9822(23)01456-2
doi: 10.1016/j.cub.2023.10.055
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIGMS NIH HHS
ID : K99 GM137038
Pays : United States
Organisme : NIGMS NIH HHS
ID : R00 GM137038
Pays : United States

Commentaires et corrections

Type : UpdateOf

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare no competing interests.

Auteurs

Kaitlin A Stromberg (KA)

Department of Pharmacology, UT Southwestern Medical Center, 6001 Forest Park Road, Dallas, TX 75390, USA.

Tristan Spain (T)

Department of Pharmacology, UT Southwestern Medical Center, 6001 Forest Park Road, Dallas, TX 75390, USA.

Sarah A Tomlin (SA)

Division of Basic Sciences, Fred Hutchinson Cancer Center, 1100 Fairview Avenue North, Seattle, WA 98109, USA; Howard Hughes Medical Institute, Fred Hutchinson Cancer Center, 1100 Fairview Avenue North, Seattle, WA 98109, USA.

Jordan Powell (J)

Department of Pharmacology, UT Southwestern Medical Center, 6001 Forest Park Road, Dallas, TX 75390, USA.

Kristen Dominique Amarillo (KD)

Department of Pharmacology, UT Southwestern Medical Center, 6001 Forest Park Road, Dallas, TX 75390, USA.

Courtney M Schroeder (CM)

Department of Pharmacology, UT Southwestern Medical Center, 6001 Forest Park Road, Dallas, TX 75390, USA. Electronic address: courtneym.schroeder@utsouthwestern.edu.

Classifications MeSH