<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16(1)</volume><submitter>Lumsden AL</submitter><funding>Centre for Neuroscience</funding><funding>Flinders School of Medicine, Nursing and Health Sciences</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Huntingtin-associated Protein 1 (HAP1) is expressed in neurons and endocrine cells, and is critical for postnatal survival in mice. HAP1 shares a conserved "HAP1_N" domain with TRAfficking Kinesin proteins TRAK1 and TRAK2 (vertebrate), Milton (Drosophila) and T27A3.1 (C. elegans). HAP1, TRAK1 and TRAK2 have a degree of common function, particularly regarding intracellular receptor trafficking. However, TRAK1, TRAK2 and Milton (which have a "Milt/TRAK" domain that is absent in human and rodent HAP1) differ in function to HAP1 in that they are mitochondrial transport proteins, while HAP1 has emerging roles in starvation response. We have investigated HAP1 function by examining its evolution, and upstream gene promoter sequences. We performed phylogenetic analyses of the HA</pubmed_abstract><journal>BMC evolutionary biology</journal><pagination>214</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5064798</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Huntingtin-associated protein 1: Eutherian adaptation from a TRAK-like protein, conserved gene promoter elements, and localization in the human intestine.</pubmed_title><pmcid>PMC5064798</pmcid><pubmed_authors>Pezos N</pubmed_authors><pubmed_authors>Young RL</pubmed_authors><pubmed_authors>Keating DJ</pubmed_authors><pubmed_authors>Lumsden AL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Huntingtin-associated protein 1: Eutherian adaptation from a TRAK-like protein, conserved gene promoter elements, and localization in the human intestine.</name><description>&lt;h4>Background&lt;/h4>Huntingtin-associated Protein 1 (HAP1) is expressed in neurons and endocrine cells, and is critical for postnatal survival in mice. HAP1 shares a conserved "HAP1_N" domain with TRAfficking Kinesin proteins TRAK1 and TRAK2 (vertebrate), Milton (Drosophila) and T27A3.1 (C. elegans). HAP1, TRAK1 and TRAK2 have a degree of common function, particularly regarding intracellular receptor trafficking. However, TRAK1, TRAK2 and Milton (which have a "Milt/TRAK" domain that is absent in human and rodent HAP1) differ in function to HAP1 in that they are mitochondrial transport proteins, while HAP1 has emerging roles in starvation response. We have investigated HAP1 function by examining its evolution, and upstream gene promoter sequences. We performed phylogenetic analyses of the HA</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Oct</publication><modification>2026-06-08T03:21:26.783Z</modification><creation>2019-03-27T02:26:43Z</creation></dates><accession>S-EPMC5064798</accession><cross_references><pubmed>27737633</pubmed><doi>10.1186/s12862-016-0780-3</doi></cross_references></HashMap>