AI Article Synopsis

  • Human septins 3, 9, and 12, part of the SEPT3 subgroup, are unique due to their lack of a C-terminal coiled coil and formation of octameric protofilaments, unlike other hexameric septins.
  • These septins can self-assemble into mixed filaments and form higher-order complexes with membranes, potentially influencing various cellular processes.
  • The study presents detailed crystal structures of the GTP-binding domains of SEPT3 members, revealing a mechanism for membrane interaction linked to GTP binding and hydrolysis, underscoring the special role of this subgroup in cellular functions.

Article Abstract

Human septins 3, 9 and 12 are the only members of a specific subgroup of septins that display several unusual features, including the absence of a C-terminal coiled coil. This particular subgroup (the SEPT3 septins) are present in rod-like octameric protofilaments but are lacking in similar hexameric assemblies, which only contain representatives of the three remaining subgroups. Both hexamers and octamers can self-assemble into mixed filaments by end-to-end association, implying that the SEPT3 septins may facilitate polymerization but not necessarily function. These filaments frequently associate into higher order complexes which associate with biological membranes, triggering a wide range of cellular events. In the present work, a complete compendium of crystal structures for the GTP-binding domains of all of the SEPT3 subgroup members when bound to either GDP or to a GTP analogue is provided. The structures reveal a unique degree of plasticity at one of the filamentous interfaces (dubbed NC). Specifically, structures of the GDP and GTPγS complexes of SEPT9 reveal a squeezing mechanism at the NC interface which would expel a polybasic region from its binding site and render it free to interact with negatively charged membranes. On the other hand, a polyacidic region associated with helix α5', the orientation of which is particular to this subgroup, provides a safe haven for the polybasic region when retracted within the interface. Together, these results suggest a mechanism which couples GTP binding and hydrolysis to membrane association and implies a unique role for the SEPT3 subgroup in this process. These observations can be accounted for by constellations of specific amino-acid residues that are found only in this subgroup and by the absence of the C-terminal coiled coil. Such conclusions can only be reached owing to the completeness of the structural studies presented here.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7201284PMC
http://dx.doi.org/10.1107/S2052252520002973DOI Listing

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