At
this very moment thousands of our body's cells are duplicating and dividing.
This is the mechanism by which the body repairs damaged tissues and regenerates
others like skin and hair. It involves a fairly complex process known as
"mitosis", during which the cell duplicates its genetic material and
separates it into two identical halves, which are then split apart. It is
crucially important that this process works well each and every time it takes
place, as otherwise it could give rise to mutations that might trigger diseases
such as cancer.
Work
published today in the Journal of Cell Biology and carried out by a team of
researchers from the Centre for Genomic Regulation (CRG) sheds new and
revealing light on this complex mechanism. In a study using yeast, they have
discovered that an enzyme known to be vital for chromosome separation,
topoisomerase 2 (Topo 2), is active for much longer than was previously
thought; they have also observed that chromosome length is decisive in
determining the amount of time this protein works
for.
See also: A new quality control pathway in the cell
See also: A new quality control pathway in the cell
Untangling chromosomes
When a cell prepares to divide, it duplicates its DNA and compacts it into
pairs of identical chromosomes. However these duplicated chromosomes are
twisted around each other, as if they were a tangled up pair of earphones.
Before the cell is split into two, each half must receive one copy of each
replicated chromosome; it is thus essential that chromosome pairs unknot or
untangle properly. Otherwise, they will not be able to separate during cell
division, and the DNA within could be cut or divided badly, which might lead to
cell death or harmful mutations – and possibly cancer.
"To solve this problem the cell has two
options: either to patiently disentangle the chromosomes, as one unties messed
up cables; or to cut them up and put them back together again. For cables,
especially if they are earphones wires, perhaps cutting them is not a good
idea, but chromosomes are so long that there is really no other option. And
this is what the cell does using Topo 2", explains Manuel Mendoza,
head of the Coordination
of Cytokinesis with Chromosome Segregation group at the CRG.
Topo
2 is, therefore, a molecule responsible for cutting DNA knots between
replicated DNA molecules, untangling the pairs of chromosomes and closing up
the cuts afterwards, so that each member of the pair of chromosomes can migrate
to the opposite side of the cell as it splits in half. This role of Topo 2 has
been known for some time, but it was believed that it acted quickly and equally
on all chromosomes. However, Mendoza and his team suggest that this hypothesis
was wrong.
The
team of researchers from the CRG wanted to know if chromosome length influenced
this enzyme's action at all. In principle, if the number of entanglements
between the chromosomes in each cell is the same, independently of whether the
chromosomes are long or short, then the time Topo2 needs to untwine them should
always be the same too.
However,
they have found that in cells with chromosomes that are longer than normal,
Topo2 needs an extra amount of "help" to undo the knots, suggesting
it has to be active for longer. To continue with the previous metaphor,
apparently this molecule needs –although it is not known why- for the cables of
the two earphones to be stretched until the first knot is under tension: this
is when Topo2 begins to untie it. And it does this in order, knot by knot,
starting with the closest to the end of the earphones and ending with the
farthest away.
The
"help" which Topo2 receives comes from the microtubules, a type of
tiny wire that makes up part of the mitotic spindle, a structure similar to a
rugby ball that is created when the cell begins the process of duplication and
division. The microtubules are anchored to the chromosomes at a precise point
(the centromere) and pull them apart so that one copy goes to each side of the
cell. This way when it splits apart, each half will contain the same genetic
information.
Mendoza
explains that "surprisingly, we saw
that the longer a chromosome is, the more time it takes the enzyme to unknot it
completely. And we believe we understand why. As the speed at which these
microtubules pull chromosomes apart is constant, when the chromosome is short,
all the tangles or knots rapidly come under tension. On the other hand, if it
is long, it will take more time for tension to spread through the whole
chromosome", and, therefore, Topo 2 will finish to untangle
them later. To understand this process better, just imagine someone trying to
pick up and wrap a long rope.
According
to the results of this study, the long chromosomes need more time to be
disentangled than the short ones. And this untangling only occurs when the
microtubules begin to stretch the chromosomes, in the period of mitosis known
as 'anaphase'. Right up to this moment, Topo2 continues doing its job.
Understanding
all the players in the precise mechanism of cell division helps us understand
one of the most complex and repetitive processes in any organism. The correct
functioning of cell division is key to the survival of every cell and, by
extension, of all living beings.The above story provided by Center for Genomic Regulation.
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