Preventing dangerous nonsense in human gene expression

October 13, 2011 in Genetics

Human genes are preferentially encoded by codons that are less likely to be mistranscribed (or "misread") into a STOP codon. This finding by Brian Cusack and colleagues from the Max Planck Institute for Molecular Genetics in Berlin and the CNRS in Lyon and Paris is published in the open-access journal PLoS Genetics on October 13th, 2011.

Since the completion of the over a decade ago, a multitude of studies have investigated the forces that have shaped the genome over time. However, because gene expression errors are not inherited, they have been disregarded as an evolutionary force until now.

In biological systems, mistakes are made because the cellular machinery is complex and error prone. The errors made in copying DNA for transmission to offspring () have so far been the primary focus of . But errors are much more frequent in the day-to-day task of gene expression, for example in the transcription of DNA into RNA. This study shows how use a dual strategy of "prevention and cure" to deal with a specific type of gene expression error: transcriptional errors that create premature STOP codons (so-called "nonsense errors"). Nonsense errors can be highly toxic for the cell, so natural selection has evolved a strategy called nonsense-mediated decay (NMD) to "cure" such errors. However, this cure is inefficient. This work identifies a strategy of prevention that has evolved to compensate for the inefficiency of NMD by decreasing the frequency of nonsense errors. Natural selection achieves this through the avoidance of codons that are prone to nonsense errors and the preferential usage of codons robust to such errors.

Cusack et al's results provide a rationale for the evolution of robustness by implying that transcriptional errors are visible to natural selection because they are frequent and deleterious. According to the authors, "this raises the question of the past and present impact of such errors on human disease." An accompanying Perspectives article is published in on the same day.

More information: Cusack BP, Arndt PF, Duret L, Crollius HR (2011) Preventing Dangerous Nonsense: Selection for Robustness to Transcriptional Error in Human Genes. PLoS Genet 7(10): e1002276. doi:10.1371/journal.pgen.1002276

Provided by Public Library of Science search and more info website

5 /5 (1 vote)  

Rank 5 /5 (1 vote)
Relevant PhysicsForums posts

More news stories

Inherited DNA change explains overactive leukemia gene

A small inherited change in DNA is largely responsible for overactivating a gene linked to poor treatment response in people with acute leukemia.

Genetics created 22 hours ago | popularity not rated yet | comments 0 | with audio podcast

'Personality genes' may help account for longevity

"It's in their genes" is a common refrain from scientists when asked about factors that allow centenarians to reach age 100 and beyond. Up until now, research has focused on genetic variations that offer a physiological advantage ...

Genetics created May 24, 2012 | popularity 3 / 5 (1) | comments 0 | with audio podcast

Gene discovery points towards non-hormonal male contraceptive

A new type of male contraceptive could be created thanks to the discovery of a key gene essential for sperm development.

Genetics created May 24, 2012 | popularity 5 / 5 (5) | comments 0 | with audio podcast

Key gene found responsible for chronic inflammation, accelerated aging and cancer

Researchers at NYU School of Medicine have, for the first time, identified a single gene that simultaneously controls inflammation, accelerated aging and cancer.

Genetics created May 24, 2012 | popularity not rated yet | comments 0

Knowing genetic makeup may not significantly improve disease risk prediction

Harvard School of Public Health (HSPH) researchers have found that detailed knowledge about your genetic makeup—the interplay between genetic variants and other genetic variants, or between genetic variants and environmental ...

Genetics created May 24, 2012 | popularity 2 / 5 (1) | comments 0 | with audio podcast


Family history of Alzheimer's affects functional connectivity

(HealthDay) -- Cognitively normal individuals with a family history of late-onset Alzheimer's disease (AD) may display lower resting state functional connectivity in the default mode network (DMN) of the brain, ...

Travel to high altitudes tied to Crohn's, colitis flare-ups

(HealthDay) -- People with inflammatory bowel disease, which includes Crohn's disease and colitis, may be at increased risk for flare-ups when they fly or travel to high altitudes for skiing or mountain climbing, ...

Transvaginal mesh op restores pelvic organ prolapse at price

(HealthDay) -- Transvaginal mesh (TVM) procedures are effective for anatomical restoration of pelvic organ prolapse (POP), but patients report a worsening of sexual function following surgery, according to ...

Cancer may require simpler genetic mutations than previously thought

Chromosomal deletions in DNA often involve just one of two gene copies inherited from either parent. But scientists haven't known how a deletion in one gene from one parent, called a "hemizygous" deletion, can contribute ...

Tongue analysis software uses ancient Chinese medicine to warn of disease

For 5,000 years, the Chinese have used a system of medicine based on the flow and balance of positive and negative energies in the body. In this system, the appearance of the tongue is one of the measures used to classify ...

Skp2 activates cancer-promoting, glucose-processing Akt

HER2 and its epidermal growth factor receptor cousins mobilize a specialized protein to activate a major player in cancer development and sugar metabolism, scientists report in the May 25 issue of Cell.