September 13, 2002
Breast Cancer Gene Repairs Damaged DNA
Structural studies of the protein produced by the BRCA2 gene,
which is implicated in the development of hereditary breast and ovarian
cancers, reveal that the protein is intimately involved in repairing
damaged DNA.
DNA-repair proteins perform a vital function and protect against
potentially catastrophic events such as cancer-causing mutations or
chromosome rearrangements, which are hallmarks of tumor cells.
Howard Hughes Medical Institute investigator Nikola
P. Pavletich and his colleagues at Memorial Sloan-Kettering Cancer
Center used x-ray crystallography to obtain “molecular
snapshots” of the BRCA2 protein. The images produced by
Pavletich’s team show that BRCA2 is capable of binding to DNA, a
conclusion that is supported by the group’s biochemical
experiments. The research was published in the September 13, 2002,
issue of the journal Science.
The scientists were investigating the role of BRCA2 in homologous
recombination, which is one of the ways that cells repair broken
chromosomes. In this type of DNA repair, broken chromosomes are fixed
by using the information from a sister chromosome as a template and
“splint” to guide repair. This type of DNA repair is
accurate and is the optimal mode of repair in dividing cells. Prior to
the studies by Pavletich and his colleagues, BRCA2 was believed to play
only an indirect regulatory role in DNA repair.
“BRCA2 had been previously implicated in the control of
homologous recombination, although its precise role in this process was
unknown,” said HHMI investigator Stephen
J. Elledge, who is at Baylor College of Medicine. “The
significance of the structural studies of BRCA2 by Pavletich’s
group is that they provide evidence for a direct and unexpected
biochemical role for BRCA2 in the enzymology of homologous
recombination itself. It was an elegant study that will forever change
the way we think about BRCA2 and its role in breast cancer.”
Elledge authored an accompanying article in Science that
discusses the implications of the findings by Pavletich and his
colleagues.
Pavletich’s team encountered several major technical hurdles,
the first of which involved producing a segment of the BRCA2 protein —
called the C-terminal end. “We chose this fragment because of
evidence — based on its amino acid sequence, on the fact that it is
conserved in many organisms, and on the fact that it is often mutated
in tumors — that it carries out an important function in
homologous-recombination-mediated repair,” said Pavletich.
Producing this large protein fragment of BRCA2 and crystallizing it
for x-ray crystallographic studies was a formidable challenge. Lead
author Haijuan Yang got a break when she identified a
“companion” protein called DSS1 that bound to the BRCA2
fragment and made it amenable to crystallization.
The scientists then used x-ray crystallography to determine the
detailed structure of the BRCA2 fragment. In this process, x-ray beams
are directed through purified crystals of a protein, and the resulting
patterns of diffraction are analyzed to deduce the protein’s
structure.
“Once we analyzed the structure and compared it with known
protein structures, it had domains that looked familiar,” said
Pavletich. “These domains, called oligonucleotide binding folds,
are found in proteins known to bind single-stranded DNA.”
The scientists then conducted biochemical binding tests in
vitro using the BRCA2 domain, which revealed that the BRCA2
fragment did indeed bind single-stranded DNA. This finding was
confirmed by additional studies in which the researchers crystallized
the BRCA2 fragment bound to single-stranded DNA. According to
Pavletich, the experiments provided strong evidence that BRCA2 is
intimately involved with DNA binding in the repair process.
The researchers discovered that another domain in the BRCA2 fragment
binds double-stranded DNA, although they have not yet established
conclusively that the domain by itself binds double-stranded DNA.
Pavletich’s group also showed that BRCA2 stimulates the
activity of an enzyme called RAD51 recombinase, a key component of the
DNA-repair machinery. “Our observations taken together with other
data, suggest that BRCA2 is what recognizes double-strand
breaks,” said Pavletich. “When a cell encounters a
double-strand break, it chews up that break to produce single-stranded
DNA at the end of double-stranded DNA. And this is what we think is
recognized by BRCA2, since it has both single-stranded and
double-stranded DNA binding activity.
“We were surprised at this direct role of BRCA2, because among
scientists in the field, [BRCA2] was thought to be the regulator of
RAD51. This function of BRCA2 was more in line with BRCA1, which is
thought to be a signaling protein in the process,” said
Pavletich. Mutations in BRCA1 also have been implicated in the
development of breast and other cancers.
Pavletich added that “our findings don’t reveal any
obvious treatment strategies, but as with all basic science, studying
how a process works, and how it malfunctions in cancer brings us closer
to understanding the process of tumorigenesis.” Thus, he said,
his laboratory plans detailed studies of how the DNA-binding domain of
BRCA2 works in concert with the separate domain that binds to RAD51, in
triggering the DNA-repair machinery.
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