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Research Reveals Role
of Gene in Infertility
A paper describing discoveries about the role of a gene that is
important in all animals, plants, and fungi was published in the
journal Proceedings of the National
Academy of Sciences. One of
the discoveries is that the gene, named RAD51, plays an essential
role in the process of recombining the genetic material in chromosomes
during sexual reproduction in plants. In humans, defects in this
process can cause a fetus to have abnormal numbers of chromosomes,
resulting in infertility, miscarriages, or birth defects. The new
discoveries about the gene’s role in plants suggest that
it also may have an essential role in the production of sperm and
egg cells in humans and other mammals.
One of the most surprising
results of the research is that the RAD51 gene is not essential
for survival in plants, as it is known to be in mammals. “It
is well known that a mouse fetus that inherits two defective copies
of the RAD51 gene will die very soon after conception, so we were
quite surprised to find that our mutant plants, which have two
defective copies of this gene, develop quite normally—except
that they are sterile,” reports Hong
Ma, professor of biology at Penn
State and the leader of the research
team that made the discoveries in collaboration with the Bernd
Reiss group at the Max-Planck
Institute for Plant Breeding Research in Germany.
The team’s work reveals specific functions of
the protein products of the RAD51 gene, including the pairing of
compatible chromosomes—the structures that contain the cell’s
genes—during the process of meiosis, when an organism’s
reproductive cells form during its development, and also the repairing
of breaks in the chromosomes that occur during this and other process. “Our
research leads us to suspect that plant cells repair breaks in
their DNA in a different way from mammal cells, which just stop
growing if the RAD51 gene is not functioning,” Ma says.
Meiosis
produces the cells of sexual reproduction, such as sperm cells
and egg cells, which contain only a single strand of each of the
organism’s characteristic number of chromosomes. Later,
when the mature sperm and egg cells combine, the new individual
will have its full complement of DNA—half from the mother
and half from the father. Much of the team’s research is
focused on the reshuffling of genetic material between two similar
chromosomes, which occurs during meiosis when the double-stranded
chromosomes in the cell’s nucleus are pulled apart and brought
together again twice by a team of proteins, resulting in four new
male or female reproductive cells.
The researchers conduct their
studies with a mutant strain of the model laboratory plant, Arabidopsis,
in which the RAD51 gene is unable to function because a piece of
foreign DNA is inserted in the middle of the gene. Ma’s team
dissected the plant’s
tiny flower buds before they had a chance to develop, when they
were only about 0.3 or 0.4 millimeters in diameter. “It is
important to look at the cells from the tiny flower buds before
they open because meiosis is an event that occurs before pollen
development starts,” Ma explains. “We then treat the
cells with chemicals that protect their structure from damage and
then stain them with a chemical that allows us to see the DNA much
more clearly than any other part of the cell.”
The researchers’ microscopic
images of meiosis in their mutant plants revealed not neat chromosome
packages but a chaos of many broken sections of chromosomes. “We
found that plants in which the RAD51 gene does not function are
not able to recombine the sections of their chromosomes that are
broken during meiosis,” Ma
says. The researchers additionally tested this finding by introducing
into the plants a mutation in a gene, named SPO-11, that disables
the protein system that cuts chromosomes. “In plants that
are defective in both SPO-11 and RAD51, we find intact chromosomes,
not the jumble of chromosome fragments,” Ma reports. “Because
the chromosomes are not cut in the first place, you don’t
really need the RAD51 to repair it.” These experiments demonstrate
that RAD51 has an essential role in the biochemical repair of DNA
during recombination. They also establish that this system for
repairing broken chromosomes, which previously was known to occur
in animals and fungi, occurs in plants, as well.
The RAD51 gene
codes for a type of enzyme known as a recombinase, which catalyzes
the swapping, or “crossover,” of DNA
sections between very similar, or “homologous” chromosomes.
At conception, an individual inherits one copy of a chromosome
from its father and another very similar but not exactly identical
copy from its mother. This DNA swapping—a process known as
recombination—is important for generating diversity among
individuals within the same family and throughout the entire population.
These very similar molecules of DNA, along which specific genes
lie at the same point on each strand, are brought together by the
molecular machinery of the cell to form a two-chromosome structure
known as a homologous pair. Because the DNA along each chromosome
is so similar, a thin structure is able to form between the chromosomes
resulting in a structure known as a synaptonemal complex, which
links the two strands together. Ma’s research is the first
to provide definitive evidence that the RAD51 gene is required
specifically for homolog pairing and synapsis, in addition to its
role in recombination during meiosis. “In the mutant, we
found that the chromosomes do not come together to form pairs,” he
reports. “Our research shows that the RAD51 protein has a
role in bringing a single strand of DNA to its counterpart within
the nucleus of a cell to form a double-strand and is a critical
component of the whole complex of proteins that holds the two strands
close to one another.”
Many of the findings of Ma’s
team’s research are revealed
in its exquisite electron-microscope images, which show more clearly
than ever before the process of cell division in plants. “We
are fortunate to have on our team a scientist who is highly skilled
at the very tricky process of preparing cells for viewing with
an electron microscope,” Ma says. Like a loaf of bread cut
into slices, the images show a section-by-section dissection of
the chromosomes that reveal their structure and position within
the cell. Clearly visible is the jelly-sandwich-like structure
known as the synaptonemal complex—a thick piece of the chromosome
sitting next to another thick piece with a thin central element
joining the two. This synaptonemal complex should form during meiosis
for the entire set of chromosomes in normal plant cells, but Ma
found that it does not form in the reproductive cells of the mutant
plant. “You just see lots of thick pieces that have not gotten
paired with another piece because RAD51 is not there to bring the
two pieces together,” Ma says. The electron-microscope images
show definitively that the RAD51 gene is required in plants for
forming the central element that pairs the two chromosomes.
The
RAD51 gene also is known to be required for its role in repairing
damage caused to DNA in all of an organism’s cells by harmful
radiation and chemicals. The cell uses an intact section of DNA
as a template for repairing a damaged homologous one. The research
establishes that this system for repairing broken chromosomes with
the protein products of the RAD51 gene, which previously was known
to occur in animals and fungi, occurs in meiotic cells of plants,
as well.
“Our research suggests that some defects in human
reproduction may be associated with partial loss of the RAD51 function,” Ma
says. “While it is not possible at present to study defects
in this RAD51 gene in people who have fertility problems, we now
can use this mutant plant strain to understand more than we could
before about its role in sexual reproduction.”
In addition
to Ma and Reiss, other members of the research team include Wuxing
Li and Changbin Chen at Penn State; Ullrich Markmann-Mulisch and
Elmon Schmelzer at the Max-Planck Institute in Germany; and Ljudmilla
Timefejeva at Penn State and the Estonian
Agricultural University.
This research was supported by grants from the U.S.
National Institutes of Health, the U.S.
National Science Foundation, the U.S.
Department of Energy, and the European
Commission.
Barbara K. Kennedy
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