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Critical Protein Prevents DNA Damage From Persisting Through Generations

Date:
July 2, 2007
Source:
Rockefeller University
Summary:
A protein called ATM, long known to be involved in protecting cells from genetic damage, is also part of a system that prevents damage from being passed on when the cells divide.
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Disappearing act: Normal chromosomes are capped by complexes called telomeres (red), which act as buffers and lose a little bit of material every time the cell divides. When scientists looked at dividing immune system B cells that lacked the ATM protein, they saw that chromosome 12 (bottom left, green spots) was missing its telomeres, a defect commonly seen in lymphomas.
Credit: Image courtesy of Rockefeller University

A protein long known to be involved in protecting cells from genetic damage has been found to play an even more important role in protecting the cell's offspring. New research by a team of scientists at Rockefeller University, Howard Hughes Medical Institute and the National Cancer Institute shows that the protein, known as ATM, is not only vital for helping repair double-stranded breaks in DNA of immune cells, but is also part of a system that prevents genetic damage from being passed on when the cells divide.

Early in the life of B lymphocytes -- the immune cells responsible for hunting down foreign invaders and labeling them for destruction -- they rearrange their DNA to create various surface receptors that can accurately identify different intruders, a process called V(D)J recombination. Now, in an study published online today in the journal Cell, Rockefeller University Professor Michel Nussenzweig, in collaboration with his brother André Nussenzweig at NCI and their colleagues, shows that when the ATM protein is absent, chromosomal breaks created during V(D)J recombination go unrepaired, and checkpoints that normally prevent the damaged cell from replicating are lost.

Normal lymphocytes contain a number of restorative proteins, whose job it is to identify chromosomal damage and repair it or, if the damage is irreparable, prevent the cell from multiplying. Earlier research by André and Michel Nussenzweig, who is an investigator at HHMI, had identified other DNA repair proteins that are important during different phases of a B lymphocyte's life. It was during one of these studies, which examined genetic damage late in the life of a B cell, that they came across chromosomal breaks that could not be explained.

So the researchers began to look into the potential role of V(D)J recombination. "We were not expecting it to be responsible for the breaks we were seeing," says Michel, Sherman Fairchild Professor and head of the Laboratory of Molecular Immunology. "Because for it to be responsible, the breaks would have had to happen early on, the cell would have to divide, mature, maintain the breaks, and stay alive with broken chromosomes."

This, in fact, was precisely what they found.

The ATM protein appears to have two roles in a B cell: It helps repair the DNA double-strand breaks, and it activates the cell-cycle checkpoint that prevents genetically damaged cells from dividing. "ATM is required for a B cell to know that it has a broken chromosome. And if it doesn't know that it seems to be able to keep on going," says Michel.

Since the ATM protein is mutated in a number of lymphomas -- cancers of the lymph and immune system -- the new finding suggests to researchers that the lymphocytes could have been living with DNA damage for a long time, and that this damage likely plays a role in later chromosomal translocations, rearrangements of genetic materials that can lead to cancer.

Michel and his brother, who've been collaborators for more than a decade, intend to pursue the molecular mechanisms by which these chromosomal translocations occur. "I think it's important to understand them," he says, "because eventually we might be able to prevent these dangerous chromosome fusions."

This research was supported by the National Institutes of Health.


Story Source:

The above story is based on materials provided by Rockefeller University. Note: Materials may be edited for content and length.


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Rockefeller University. "Critical Protein Prevents DNA Damage From Persisting Through Generations." ScienceDaily. ScienceDaily, 2 July 2007. <www.sciencedaily.com/releases/2007/06/070628183251.htm>.
Rockefeller University. (2007, July 2). Critical Protein Prevents DNA Damage From Persisting Through Generations. ScienceDaily. Retrieved May 24, 2015 from www.sciencedaily.com/releases/2007/06/070628183251.htm
Rockefeller University. "Critical Protein Prevents DNA Damage From Persisting Through Generations." ScienceDaily. www.sciencedaily.com/releases/2007/06/070628183251.htm (accessed May 24, 2015).

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