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Evolution of Human-Specific Alleles Protecting Cognitive Function of Grandmothers
- Source :
- Molecular biology and evolution, vol 39, iss 8
- Publication Year :
- 2022
- Publisher :
- Oxford University Press (OUP), 2022.
-
Abstract
- SummaryLate-onset Alzheimer’s Disease (LOAD) pathology is rare in our closest living evolutionary relatives (chimpanzees), which also express much lower microglial levels of CD33(Siglec-3)–a myelomonocytic receptor inhibiting innate immune reactivity by extracellular V-set domain recognition of sialic acid(Sia)-containing “self-associated molecular patterns” (SAMPs). We earlier showed that V-set domain-deficient CD33-variant allele, protective against LOAD, is derived and specific to hominin-lineage. We now report that CD33 also harbors multiple hominin-specific V-set domain mutations and explore selection forces that may have favored such genomic changes. N-glycolylneuraminic acid (Neu5Gc), the preferred Sia-ligand of ancestral CD33 is absent in humans, due to hominin-specific, fixed loss-of-function mutation in CMAH, which generates CMP-Neu5Gc from its precursor, CMP-N-acetylneuraminic acid (Neu5Ac). Extensive mutational analysis and MD-simulations indicate that fixed change in amino acid 21 of hominin V-set domain and conformational changes related to His45 corrected for Neu5Gc-loss by switching to Neu5Ac-recognition. Considering immune-evasive “molecular mimicry” of SAMPs by pathogens, we found that human-specific pathogens Neisseria gonorrhoeae and Group B Streptococcus (affecting fertility and fetuses/neonates respectively) selectively bind huCD33 and this binding is significantly impacted by amino acid 21 modification. Alongside LOAD-protective CD33 alleles, humans harbor additional, derived, population-universal, cognition-protective variants absent in “great ape” genomes. Interestingly, 11 of 13 SNPs in these human genes (including CD33), that protect the cognitive health of elderly populations, are not shared by genomes of archaic hominins: Neanderthals and Denisovans. Finally, we present a plausible evolutionary scenario to compile, correlate and comprehend existing knowledge about huCD33 evolution and suggest that grandmothering emerged in humans.
- Subjects :
- Single-nucleotide polymorphism
Biology
archaic genome
medicine.disease_cause
Genome
chemistry.chemical_compound
Cognition
Clinical Research
medicine
Genetics
Animals
Humans
2.1 Biological and endogenous factors
Amino Acids
Aetiology
Allele
Molecular Biology
Alleles
Ecology, Evolution, Behavior and Systematics
Evolutionary Biology
Mutation
Innate immune system
phylogenetic analysis
Human Genome
Hominidae
Sialic acid
Grandparents
Molecular mimicry
molecular dynamics simulation
chemistry
Human genome
Biochemistry and Cell Biology
CD33
sialic acids
pathogen
Subjects
Details
- ISSN :
- 15371719 and 07374038
- Volume :
- 39
- Database :
- OpenAIRE
- Journal :
- Molecular Biology and Evolution
- Accession number :
- edsair.doi.dedup.....8663eb6aa45f54c0377df5dab15144d6