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Neanderthal lineages excavated from modern human genomes

By Guest PostFebruary 8, 2014Sciencearchaic dna sequences, benjamin vernot, clare mclean, croatia, DNA, east asia, Europe, evolutionary anthropology, fossil free, genomes project, Germany, human evolution, human populations, joshua akey, joshua m akey, max planck institute, modern human genomes, neanderthal dna, neanderthal lineages, neanderthal museum, non african descent, paleogenetics laboratory, population geneticists, scientist, sequencing data, svante pääbo, university of washington

A substantial fraction of the Neanderthal genome persists in modern human populations. A new approach applied to analyzing whole-genome sequencing data from 665 people from Europe and East Asia shows that more than 20 percent of the Neanderthal genome survives in the DNA of this contemporary group, whose genetic information is part of the 1,000 Genomes Project.

Previous research proposes that someone of non-African descent may have inherited approximately 1 percent to 3 percent of his or her genome from Neanderthal ancestors. These archaic DNA sequences can vary from one person to another and were aggregated in the present study to determine the extent of the Neanderthal genome remaining in the study group as a whole. The findings are a start to identifying the location of specific pieces of Neanderthal DNA in modern humans and a beginning to creating a collection of Neanderthal lineages surviving in present-day human populations. (more…)

Harmful Protein-Coding Mutations in People arose Largely in the Past 5,000 to 10,000 Years

By Guest PostDecember 2, 2012Sciencea, africa migration, african, age, alzheimer, c, dating, discovery, dna code, dna sequence, Europe, european ancestry, evolutionary geneticist, future generation, g, gene, genetic variants, hardening, harmful, heart arteries, human, human diaspora, joshua akey, mesopotamia, metabolic pathways, middle east, model, mutation, nucleotide, out of africa, paralysis, premature ovarian failure, protein coding gene, protein coding mutation, seattle, single nucleotide, t, tap energy, university, variation, Washington, wenqing fu

A study dating the age of more than 1 million single-letter variations in the human DNA code reveals that most of these mutations are of recent origin, evolutionarily speaking. These kinds of mutations change one nucleotide – an A, C, T or G – in the DNA sequence. Over 86 percent of the harmful protein-coding mutations of this type arose in humans just during the past 5,000 to 10,000 years.

Some of the remaining mutations of this nature may have no effect on people, and a few might be beneficial, according to the project researchers. While each specific mutation is rare, the findings suggest that the human population acquired an abundance of these single-nucleotide genetic variants in a relatively short time. (more…)

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Neanderthal lineages excavated from modern human genomes

Harmful Protein-Coding Mutations in People arose Largely in the Past 5,000 to 10,000 Years