Is DNA Repair a Substitute for Sex?April 03, 2008MBL, WOODS HOLE, MA-Birds and bees may do it, but the microscopic animals called bdelloid rotifers seem to get along just fine without sex, thank you. What's more, they have done so over millions of years of evolution, resulting in at least 370 species. These hardy creatures somehow escape the usual drawback of asexuality - extinction - and the MBL's David Mark Welch, Matthew Meselson, and their colleagues are finding out how. In two related papers published this week in Proceedings of the National Academy of Sciences (PNAS), the team proposes an interesting hypothesis: Bdelloid rotifers have been able to give up sex and survive because they have evolved an extraordinary efficient mechanism for repairing harmful mutations to their DNA. "We think, in the bdelloid rotifer, genomic changes together with environmental changes have conspired to create something that is able to exist in the absence of sex," says Mark Welch, an assistant scientist in the MBL's Josephine Bay Paul Center. Their results have medical implications, because DNA repair capacity is an important factor in cancer, inflammation, aging, and other human conditions. In animals that do have sex, DNA repair is accomplished during meiosis, when chromosomes pair up (one from the father, one from the mother) and "fit" genes on one chromosome can serve as templates to repair damaged genes on the other chromosome. The bdelloid, though, always seems to reproduce asexually, by making a clone of itself. How then, does it cope with deleterious mutations? In the first PNAS paper, MBL adjunct scientist Matthew Meselson and Eugene Gladyshev, both of Harvard University, demonstrate the enormous DNA repair capacity of bdelloid rotifers by zapping them with ionizing radiation (gamma rays), which has the effect of shattering its DNA into many pieces. "We kept exposing them to more and more radiation, and they didn't die and they didn't die and they didn't die," says Mark Welch. Even at five times the levels of radiation that all other animals are known to endure, the bdelloids were able to continue reproducing. "Because there is no source of such intense ionizing radiation on Earth, except if we make it, there is no way these organisms could have evolved to be radiation resistant," says Mark Welch. Instead, they propose that bdelloids' DNA repair capacity evolved due to a different environmental adaptation - tolerance of extreme dryness. Bdelloids, which live in ephemeral aquatic habitats such as temporary freshwater pools and on mosses, are able to survive complete desiccation (drying out) at any stage of their life cycle. They just curl up and go dormant for weeks, months, or years, and when water becomes available, they spring back to life. Mark Welch and his colleagues showed that desiccation, like ionizing radiation, breaks up the rotifers' DNA into many pieces. Presumably, the same mechanisms they use to survive desiccation as part of their life cycle also protect them from ionizing radiation. "That's the next thing we are looking at. How are the bdelloids able to repair this many double-stranded breaks in their DNA? Do they have better enzymes, more enzymes?" Mark Welch says. One feature that may confer exceptional DNA repair capacity on the bdelloids is described in the team's second PNAS paper. Here, they give evidence that the bdelloid rotifer, like most animals, originally had two copies of each chromosome. But at some point in its evolution, it underwent a "whole-genome duplication," giving it four copies of each chromosome and hence of each gene. Normally, lineages that undergo whole-genome duplication lose the duplicate genes over time. The bdelloid, though, has kept most of its duplicate genes throughout its evolutionary history. "We believe they have kept most of their duplicate genes because they are serving as templates for DNA repair," says Mark Welch. One possible result of DNA repair is gene conversion, in which the gene being repaired ends up having an identical DNA sequence to the gene repairing it. This can introduce the kinds of changes into the gene pool that sex usually does. (For example, a gene coding for brown eyes may repair a gene coding for blue eyes on its paired chromosome, and end up turning the blue-eye gene into a brown-eye one.) "We think that gene conversion resulting from DNA repair resulting from adaptation to (desiccation in) its environment may provide enough of the advantages of sex that bdelloids can survive," Mark Welch says. Marine Biological Laboratory |
|||||||||||||||||||||
| Related DNA Repair Current Events and DNA Repair News Articles Cornell researchers identify a weak link in cancer cell armor The seeming invincibility of cancerous tumors may be crumbling, thanks to a promising new gene therapy that eliminates the ability of certain cells to repair themselves. Single-stranded DNA-binding protein is dynamic, critical to DNA repair Researchers report that a single-stranded DNA-binding protein (SSB), once thought to be a static player among the many molecules that interact with DNA, actually moves back and forth along single-stranded DNA, gradually allowing other proteins to repair, recombine or replicate the strands. October 15, 2009 Loss of Tumor-Suppressor and DNA-Maintenance Proteins Causes Tissue Demise, Penn Study Finds A study published in the October issue of Nature Genetics demonstrates that loss of the tumor-suppressor protein p53, coupled with elimination of the DNA-maintenance protein ATR, severely disrupts tissue maintenance in mice. As a result, tissues deteriorate rapidly, which is generally fatal in these animals. In addition, the study provides supportive evidence for the use of inhibitors of ATR in cancer therapy. Scientists decipher missing piece of first-responder DNA repair machine Scientists from the U.S. Department of Energy's Lawrence Berkeley National Laboratory and the Scripps Research Institute have uncovered the role played by the least-understood part of a first-responder molecule that rushes in to bind and repair breaks in DNA strands, a process that helps people avoid cancer. Baumann Lab demonstrates role of protein in distinguishing chromosome ends from DNA breaks The Stowers Institute's Baumann Lab has demonstrated how human cells protect chromosome ends from misguided repairs that can lead to cancer. Study supports DNA repair-blocker research in cancer therapy Scientists at Dana-Farber Cancer Institute have uncovered the mechanism behind a promising new approach to cancer treatment: damaging cancer cells' DNA with potent drugs while simultaneously preventing the cells from repairing themselves. Technique enables efficient gene splicing in human embryonic stem cells A novel technique allows researchers to efficiently and precisely modify or introduce genes into the genomes of human embryonic stem cells (ESCs) and induced pluripotent stem (iPS) cells, according to Whitehead scientists. Protein plays unexpected role protecting chromosome tips A protein specialist that opens the genomic door for DNA repair and gene expression also turns out to be a multi-tasking workhorse that protects the tips of chromosomes and dabbles in a protein-destruction complex, a team lead by researchers at The University of Texas M. D. Anderson Cancer Center reports in the Aug. 13 edition of Molecular Cell. Raising the alarm when DNA goes bad Our genome is constantly under attack from things like UV light and toxins, which can damage or even break DNA strands and ultimately lead to cancer and other diseases. IAU0916: The violent youth of solar proxies steer course of genesis of life One of the hottest topics at this year's XXVIIth General Assembly of the International Astronomical Union (IAU) in Rio de Janeiro, Brazil involves the study of the astrophysical conditions favourable for the development and survival of primordial life. More DNA Repair Current Events and DNA Repair News Articles |
|||||||||||||||||||||
|
|||||||||||||||||||||
|
|||||||||||||||||||||