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Proteolytic activation of human-specific Olduvai domains by the furin protease.


ABSTRACT: Olduvai protein domains (formerly DUF1220) show the greatest human-specific increase in copy number of any coding region in the genome and are highly correlated with human brain evolution and cognitive disease. The majority of human copies are found within four NBPF genes organized in a variable number of a tandemly arranged three-domain blocks called Olduvai triplets. Here we show that these human-specific Olduvai domains are posttranslationally processed by the furin protease, with a cleavage site occurring once at each triplet. These findings suggest that all expanded human-specific NBPF genes encode proproteins consisting of many independent Olduvai triplet proteins which are activated by furin processing. The exceptional correlation of Olduvai copy number and brain size taken together with our new furin data, indicates the ultimate target of selection was a rapid increase in dosage of autonomously functioning Olduvai triplet proteins, and that these proteins are the primary active agent underlying Olduvai's role in human brain expansion.

SUBMITTER: Pacheco A 

PROVIDER: S-EPMC10038901 | biostudies-literature | 2023 Apr

REPOSITORIES: biostudies-literature

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Proteolytic activation of human-specific Olduvai domains by the furin protease.

Pacheco Ashley A   Issaian Aaron A   Davis Jonathan J   Anderson Nathan N   Nemkov Travis T   Paukovich Natasia N   Henen Morkos A MA   Vögeli Beat B   Sikela James M JM   Hansen Kirk K  

International journal of biological macromolecules 20221226


Olduvai protein domains (formerly DUF1220) show the greatest human-specific increase in copy number of any coding region in the genome and are highly correlated with human brain evolution and cognitive disease. The majority of human copies are found within four NBPF genes organized in a variable number of a tandemly arranged three-domain blocks called Olduvai triplets. Here we show that these human-specific Olduvai domains are posttranslationally processed by the furin protease, with a cleavage  ...[more]

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