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Genomic benchmarking studies reveal variations of the polyubiquitination domain of the PSD95 protein in Homo neanderthalensis and other primates of the Hominidae family: Possible implications in cognitive functions?

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dc.contributor.author Zuarez Chamba, Michael
dc.contributor.author Puma Vaque, Luis Humberto
dc.contributor.author Bermeo, Jorge
dc.contributor.author Andrade, Eugenio
dc.contributor.author Bermúdez Puga, Stalin A.
dc.contributor.author Naranjo Briceño, Leopoldo
dc.date.accessioned 2021-05-14T19:30:49Z
dc.date.available 2021-05-14T19:30:49Z
dc.date.issued 2021
dc.identifier.citation Naranjo, Leopoldo. (2021). Genomic benchmarking studies reveal variations of the polyubiquitination domain of the PSD95 protein in Homo neanderthalensis and other primates of the Hominidae family: Possible implications in cognitive functions?. Bionatura. 6. 10.21931/RB/2021.06.01.23. es
dc.identifier.uri 10.21931/RB/2021.06.01.23.
dc.identifier.uri http://repositorio.ikiam.edu.ec/jspui/handle/RD_IKIAM/433
dc.description.abstract Modern humans' unique cognitive abilities regarding Neanderthals and other primate's lineages are frequently attributed to the differences in brain size development and evolution. However, recent studies have established the critical role of genomic and genetic benchmarking in analyzing the cognitive evolution between modern humans and primates, focused mainly on searching for involved genes in neurogenesis. PSD95 protein (named PSD95p) has a key role in modulating synaptic plasticity, learning, and memory skills. Thus, the present study aimed to determine the possible variations of the PSD95 gene between modern humans, Neanderthals, and other hominid primate species using bioinformatics tools. The results showed 14 polymorphisms compared with the contemporary human PSD95 gene, of which 13 were silent mutations, and only one was a non-silent mutation at the nucleotide position 281. Despite polymorphisms found at the nucleotide sequences, the PSD95p of humans and chimpanzees are 100% identical. Likewise, the gorilla and orangutan PSD95p are 100% identical, although a 103-amino acid deletion characterizes them at the N-terminal end (1-103), suggesting that it behaves like a non-functional protein. Interestingly, the single nucleotide polymorphism (SNP) found at position 281 in the Neanderthal PSD95 gene leads to a change of the E94 to valine V94 in the polyubiquitination domain (PEST) and variation in the three-dimensional structure of PSD95 protein. We prompt that this structural change in the PEST domain could induce a loss of PSD95p function and, therefore, an alteration in synaptic plasticity forms such as long-term potentiation (LTP) and long-term depression (LTD). These findingsopen a possible hypothesis supporting the idea that humans' cognitive evolution after separating our last common ancestor with Neanderthals lineage could have been accompanied by discrete changes in the PSD95p polyubiquitination domain es
dc.language.iso en es
dc.publisher Scopus es
dc.relation.ispartofseries PRODUCCIÒN CIENTÍFICA - ARTÍCULO CIENTÍFICO;A-IKIAM-000314
dc.rights openAccess es
dc.rights Atribución-NoComercial-SinDerivadas 3.0 Estados Unidos de América *
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/3.0/us/ *
dc.subject Evolution es
dc.subject Cognitive development es
dc.subject Intelligence es
dc.subject Memory es
dc.subject ARC gene es
dc.subject PES es
dc.title Genomic benchmarking studies reveal variations of the polyubiquitination domain of the PSD95 protein in Homo neanderthalensis and other primates of the Hominidae family: Possible implications in cognitive functions? es
dc.type Article es


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