PCDH11Y

PCDH11Y
Identifiers
Aliases	PCDH11Y, PCDH-PC, PCDH22, PCDHX, PCDHY, protocadherin 11 Y-linked
External IDs	OMIM: 400022; GeneCards: PCDH11Y
Gene location (Human) Chr. Y chromosome (human) Band Yp11.2 Start 5,000,226 bp End 5,742,224 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in testicle corpus callosum prefrontal cortex thoracic aorta Brodmann area 9 ascending aorta primary visual cortex Descending thoracic aorta ventricular zone temporal lobe n/a More reference expression data BioGPS n/a
Gene ontology Molecular function calcium ion binding Cellular component integral component of membrane plasma membrane membrane integral component of plasma membrane Biological process homophilic cell adhesion via plasma membrane adhesion molecules cell adhesion Sources:Amigo / QuickGO
Orthologs Databases NCBI: entry; OMA: entry Species Human Mouse Entrez 83259 n/a Ensembl ENSG00000099715 n/a UniProt Q9BZA8 n/a RefSeq (mRNA) NM_001278619 NM_032971 NM_032972 NM_032973 NM_001395587 n/a RefSeq (protein) NP_001265548 NP_116753 NP_116754 NP_116755 n/a Location (UCSC) Chr Y: 5 – 5.74 Mb n/a PubMed search n/a
Wikidata
View/Edit Human

PCDH11Y is a Y-linked gene in the genus Homo that encodes protocadherin 11Y, a protein that guides the development of nerve cells. It is the Y-chromosomal paralog of PCDH11X, which is located on the X chromosome and thus common to both sexes in humans and some of our nearest relatives including chimpanzees. 11X/Y are cadherin family genes, cell-adhesion molecules involved in neuronal signalling which attach to the surface of neurons. The X- and Y-isoforms respond in different ways to retinoic acid, a chemical involved in the development of embryos, which stimulates the activity of 11Y but suppresses that of 11X. It is one possible contributor towards the sex-biased neurophysiology of humans.

Relevance to human evolution

It has been calculated that 11X transposed from the X to Y chromosome around three million years ago, perhaps coincident with the evolutionary expansion of human brain size and the first use of stone tools. A new intron and inversion also occurred in the 11Y around 120,000 to 200,000 years ago, coincident with the period of modern human expansion out of Africa (from which all non-African humans descend) and the onset of anthropologically modern culture termed behavioral modernity.

British psychiatrist Tim Crow, who worked on the evolution of human psychiatric disease such as schizophrenia, proposed the gene is a major contributor to lateralisation, which he believed underlies human cognitive abilities. Humans are a strong outlier in brain lateralisation among primates, which among other effects gives rise to our relatively unique handedness trait. Further, there is a substantial bias towards right-handedness in all modern humans as compared to chimpanzees: 90% of humans will use their right hands for minor motor tasks, whereas chimpanzees display no preference. Crow suggested this precludes a random or cultural origin for right-preference, adding that true ambidexterity is associated with developmental delay and psychosis.