‘Runaway’ development could compromise function of the aging brain
July 20th, 2010 - 5:30 pm ICT by ANIWashington, July 20 (ANI): “Runaway” development in the brain is a potentially significant factor in age-related loss of function, found a new study.
Researchers have now identified a gene regulatory link between changes in the young and aging brain.
The brain undergoes rapid growth and development in the early years of life and then degenerates as we progress into old age, yet little is known about the biological processes that distinguish brain development and aging.
Underlying brain development is the complex and coordinated process of gene regulation.
“In development, many genes are turned on and off by regulators, such as transcription factors and microRNAs. The question is, do all of these regulatory processes cease once adulthood is reached, or are they still active in aging?” said Mehmet Somel, postdoctoral researcher at the Shanghai Institutes for Biological Sciences.
The researchers investigated messenger RNA (mRNA), microRNA, and protein expression changes in the prefrontal cortex of humans and rhesus macaque monkeys over the life span of each species.
The group found that distinct patterns of gene regulation in the prefrontal cortex do not stop at maturity, instead persisting into old age, a phenomenon that was observed for many different functional processes.
Previous work has shown that neuronal genes gradually lose activity with age, attributed to an accumulation of damage in neuronal cells over a lifetime.
The researchers showed that this process begins as early as three to four years of age, suggesting that these changes may be normal developmental regulation that continues long into old age.
While this regulation is likely to be beneficial during development, at old age continuation of the gene regulation, or “runaway” development, might be detrimental.
Interestingly, they found the runaway neuronal development to be conserved in macaques, but it occurs an accelerated rate.
Because the regulatory processes progress much faster, the authors suggest that this could be a significant contributor toward limiting the life span of macaques to only about one-third that of humans. (ANI)
- Previously unknown natural mechanism behind cocaine addiction uncovered - Jul 08, 2010
- Gene variant role in Parkinson's discovered - Aug 01, 2010
- Autism effects may be reversible - Apr 24, 2010
- New molecule may save brain cells from neurodegeneration, stroke - Jan 19, 2011
- How ovarian cancer resists chemotherapy - Mar 03, 2011
- Scientist converts skin cells into brain cells - Jul 29, 2011
- Gene makes ovarian cancer resistant to chemotherapy - Mar 03, 2011
- Micro-RNA that regulates insulin in obesity identified - Apr 01, 2011
- Function of novel molecule that underlies human deafness revealed - Jan 22, 2011
- Tuning cocaine addiction in mice - Jul 20, 2010
- Key step in body's ability to make red blood cells found - Aug 01, 2010
- Genes X-ray brings 'personalized medicine' closer to reality - Oct 08, 2010
- Scientists discover signaling pathway which ensures that plants remember to flower - Aug 21, 2009
- MicroRNAs could increase amputation risk in diabetics - Jan 13, 2011
- Chronic drinking can disrupt body clock - Aug 25, 2010
Tags: aging brain, brain development, distinct patterns, functional processes, gene regulation, life span, macaques, messenger rna, microrna, neuronal cells, neuronal development, postdoctoral researcher, prefrontal cortex, protein expression, regulatory processes, rhesus macaque monkeys, runaway development, shanghai institutes, study researchers, transcription factors