Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/24443
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dc.contributor.authorYoung, Neil D-
dc.contributor.authorHarris, Tiffany J-
dc.contributor.authorEvangelista, Marco-
dc.contributor.authorTran, Sharon-
dc.contributor.authorWouters, Merridee A-
dc.contributor.authorSoares da Costa, Tatiana P-
dc.contributor.authorKershaw, Nadia J-
dc.contributor.authorGasser, Robin B-
dc.contributor.authorSmith, Brian J-
dc.contributor.authorLee, Erinna F-
dc.contributor.authorFairlie, Walter Douglas-
dc.date2020-
dc.date.accessioned2020-09-28T20:38:23Z-
dc.date.available2020-09-28T20:38:23Z-
dc.date.issued2020-08-28-
dc.identifier.citationCommunications Biology 2020; 3(1): 478en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/24443-
dc.description.abstractEarly studies of the free-living nematode C. elegans informed us how BCL-2-regulated apoptosis in humans is regulated. However, subsequent studies showed C. elegans apoptosis has several unique features compared with human apoptosis. To date, there has been no detailed analysis of apoptosis regulators in nematodes other than C. elegans. Here, we discovered BCL-2 orthologues in 89 free-living and parasitic nematode taxa representing four evolutionary clades (I, III, IV and V). Unlike in C. elegans, 15 species possess multiple (two to five) BCL-2-like proteins, and some do not have any recognisable BCL-2 sequences. Functional studies provided no evidence that BAX/BAK proteins have evolved in nematodes, and structural studies of a BCL-2 protein from the basal clade I revealed it lacks a functionally important feature of the C. elegans orthologue. Clade I CED-4/APAF-1 proteins also possess WD40-repeat sequences associated with apoptosome assembly, not present in C. elegans, or other nematode taxa studied.en
dc.language.isoeng-
dc.titleDiversity in the intrinsic apoptosis pathway of nematodes.en
dc.typeJournal Articleen
dc.identifier.journaltitleCommunications Biologyen
dc.identifier.affiliationFaculty of Veterinary and Agricultural Sciences, The University of Melbourne, Parkville, VIC, Australiaen
dc.identifier.affiliationLa Trobe Institute for Molecular Science, La Trobe University, Melbourne, VIC, 3086, Australiaen
dc.identifier.affiliationProCanĀ®, Children's Medical Research Institute, Faculty of Medicine and Health, The University of Sydney, Westmead, NSW, Australiaen
dc.identifier.affiliationSchool of Cancer Medicine, La Trobe University, Melbourne, VIC, 3084, Australiaen
dc.identifier.affiliationOlivia Newton-John Cancer Research Institute, Heidelberg, VIC, 3084, Australiaen
dc.identifier.affiliationThe Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, 3052, Australiaen
dc.identifier.doi10.1038/s42003-020-01208-5en
dc.type.contentTexten
dc.identifier.orcid0000-0001-8756-229Xen
dc.identifier.orcid0000-0002-2121-912Xen
dc.identifier.orcid0000-0002-4423-1690en
dc.identifier.orcid0000-0003-0498-1910en
dc.identifier.orcid0000-0003-1255-9808en
dc.identifier.orcid0000-0002-2498-1160en
dc.identifier.pubmedid32859965-
local.name.researcherFairlie, Walter Douglas
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
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