Gene variant may be responsible for human learning
By New Scientist,
New Scientist
| 05. 13. 2007
Humans have a unique variant of a gene linked with learning and memory. This may help explain how we rapidly cut loose in intellect and language from our closest relatives.
The gene, KLK8, makes the protein neuropsin II, which in mice is vital for memory and learning. Bing Su and his colleagues at the Kunming Institute of Zoology in China had earlier demonstrated that neuropsin II is made by humans but not by lesser apes and old-world monkeys. Now they have shown that orang-utans and chimpanzees don't make it either (Human Mutation, DOI: 10.1002/humu.20547).
KLK8 is the first human-specific discovery of a "splice variant" - a gene that is roughly the same in different species but is "cut and pasted" differently when it is expressed, resulting in proteins with new functions. Su's team have shown that KLK8 arose through a single mutation in DNA when a thymine nucleotide was exchanged for an adenine.
This small change had a huge impact, causing 45 additional amino acids to be loaded into the protein that the gene expresses. The changes make humans' neuropsin...
Related Articles
By David Jensen, California Stem Cell Report | 02.10.2026
Touchy issues involving accusations that California’s $12 billion gene and stem cell research agency is pushing aside “good science” in favor of new priorities and preferences will be aired again in late March at a public meeting in Sacramento.
The...
By Lauren Hammer Breslow and Vanessa Smith, Bill of Health | 01.28.2026
On Jan. 24, 2026, the New York Times reported that DNA sequences contributed by children and families to support a federal effort to understand adolescent brain development were later co-opted by other researchers and used to publish “race science”...
By Arthur Lazarus, MedPage Today | 01.23.2026
A growing body of contemporary research and reporting exposes how old ideas can find new life when repurposed within modern systems of medicine, technology, and public policy. Over the last decade, several trends have converged:
- The rise of polygenic scoring...
By Stephanie Pappas, LiveScience | 01.15.2026
Genetic variants believed to cause blindness in nearly everyone who carries them actually lead to vision loss less than 30% of the time, new research finds.
The study challenges the concept of Mendelian diseases, or diseases and disorders attributed to...