RT Journal Article SR Electronic T1 Cognitive Domains Function Complementation by NTNG Gene Paralogs JF bioRxiv FD Cold Spring Harbor Laboratory SP 034645 DO 10.1101/034645 A1 Pavel Prosselkov A1 Denis Polygalov A1 Qi Zhang A1 Thomas J. McHugh A1 Shigeyoshi Itohara YR 2015 UL http://biorxiv.org/content/early/2015/12/17/034645.abstract AB Gene duplication was proposed by S.Ohno (Ohno, 1970) as a key mechanism of a gene function evolution. A pair of gene paralogs, NTNG1 and NTNG2, sharing identical gene and protein structures and encoding similar proteins, forms a functional complement subfunctionalising (SF) within cognitive domains and forming cognitive endophenotypes, as detected by Intellectual Quotient (IQ) tests (Prosselkov et al., in press). NTNG paralogs are associated with autism spectrum disorder (ASD), bipolar disorder (BD) and schizophrenia (SCZ), with unique non-overlapping segregation among the other 15 cognitive disorders (CD), emphasizing an evolutionary gain-dependent link between advanced cognitive functions and concomitant cognitive pathologies. Complementary expression and human brain transcriptome composition of the paralogs explains the observed phenomena of their functional complementarity. The lowest identity among NTNGs is found in a middle of encoded by them proteins designated as uknown (Ukd) domain. NTNG1 contains anthropoid-specific constrained regions and both genes contain non-coding conserved sequences underwent accelerated evolution in human. NTNG paralogs SF perturbates “structure drives function” concept at protein and gene levels. Their function diversification results in a so-called “Cognitive Complement (CC)” formation, a product of gene duplication and subsequent cognitive subfunction bifurcation among the NTNG gene duplicates.