In practice the clumping of genes into yarns serves to bring general
functionality into close proximity. So
we now understand that we have a 'yarn' making operator working on the
chromosome. Up to this point I had
assumed that actions were driven by independent operators separate from the
chromosomes. This is an additional tool
capable of a wide range of discrete outcomes.
It it repeated exactly over separate individuals?
The efforts to understand the genetic code continue to challenge our
imagination. When you see a pattern it
is impossible to not look for ways to manage that pattern. This appears to advance process efficiency
hugely.
The interesting philosophical problem here is that this is clearly a
reversal of entropy on the face of it.
For once the hand of GOD appears as a realistic fall back intellectual
position as is inevitable when entropy appears to be violated.
What we really know here is that it is really going to be complicated
to explain. Molecules just do not
organize themselves this smartly.
Discovery reveals
chromosomes organize into 'yarns'
by Staff Writers
Chromosomes, the molecular
basis of genetic heredity, remain enigmatic 130 years after their discovery in
1882 by Walther Flemming. New research published online in Nature by the team
of Edith Heard, PhD, from the Curie Institute and Job Dekker, PhD, from the
University of Massachusetts Medical School (UMMS), reveals a new layer in the
complex organization of chromosomes.
The scientists have shown that
chromosomes fold in a series of contiguous "yarns" that harbor groups
of genes and regulatory elements, bringing them in contact with each other and
allowing them to work in a coordinated manner during development.
Chromosomes are relatively
large molecules that, when spread out, can measure up to the length of an
entire human arm. Despite their size, however, they are actually confined
within the small space of the cell nucleus which is just a few micrometers in
size.
Furthermore, within each cell
nucleus are multiple chromosomes. In humans, for example, there are 23 pairs of
chromosomes. In order to fit all this material into this small area,
chromosomes are folded, compacted and mingled in the three-dimensional space of
the nucleus.
So do chromosomes fill the
nucleus just like spaghetti fills a plate? "Not quite," said Elphege
Nora, PhD, a post-doctoral fellow on the team of Dr. Heard, head of the
Genetics and Developmental Biology Lab at the Curie Institute. "Chromosome
folding follows a pattern, and this actually turns out to be important for
ensuring their proper function."
A chromosome looks like a
series of tiny yarns
"We have known for decades that the DNA of individual genes is wrapped around nucleosomes to form the classical 'beads-on-a-string' structure," said Dekker, co-director of the Program in Systems Biology at UMMS.
"Our new study now shows
that these beads-on-a-string subsequently fold up to form 'yarns-on-a-string,'
where each yarn is a group of genes. This domainal organization of chromosomes
represents a previously unknown higher order level of folding that we believe
is a fundamental organizing principle of genomes."
These globule-like yarns span
anything from a few hundred thousand to a million base pairs, explained Heard.
Base pairs (abbreviated as A, C, G and Ts) are the genome's unit of
measurement, and a person's DNA consists of over 3 billion pairs.
"The real surprise,
however, lies in how this spatial folding of chromosomes links up to their
functional organization," said Heard. "This chromosome folding
pattern brings together, into the same 'yarn,' several genes, up to 10 of them,
or even more."
However, there are not just
genes in these yarns. So called "regulatory genomic elements," that
can control the activity of neighboring genes like switches are also found
clustered together with the genes in these chromosomal yarns.
A group of genes belonging to
the same yarn will therefore be likely to contact a similar set of regulatory
elements, and this can result in the coordinated activity of these genes during
development.
These new observations shed
some light on several long-standing mysteries of genetics, such as the reason
why some DNA mutations can end up affecting genes that are located thousands or
even a million base pairs away.
"The cell nucleus is
packed with genes, and the cell is faced with the challenge to turn on or off
each one of them correctly," said Dekker. "By organizing groups of
genes in isolated domains, or yarns that do not mingle or mix with other genes,
the cell has solved the problem of how to regulate groups of genes coordinately
and without interference from other genes."
However, damaging one of these
"chromosome yarns" can lead to the misbehavior of all the genes it
contains.
"The three-dimensional
organization of chromosomes allows distal genomic elements to be brought
together and to functionally interact with each other. At certain points during
development it is thus possible to precisely orchestrate the activity of genes
that are far away from each other on the linear chromosome thread, but that are
actually in contact physically, within a chromosome yarn," said Nora.
"The down side of this
type of organization is that a single mutation altering the organization of
such a 'chromosome yarn' can affect a whole group of genes."
Three-dimensional folding
provides shortcuts through the chromosome
"Together with Job Dekker, who has pioneered chromosome conformation capture technologies, we have discovered these principles by studying a critical region of the X chromosome, the X-inactivation center," said Heard.
"Together with Job Dekker, who has pioneered chromosome conformation capture technologies, we have discovered these principles by studying a critical region of the X chromosome, the X-inactivation center," said Heard.
"Thanks to a parallel
study conducted by the team of Bing Ren, PhD, at the University of San Diego
(and published in Nature alongside the Heard and Dekker study), we now know
that the principles of chromosome folding we have seen on the X chromosome
actually apply to the whole mouse and human genomes."
Beyond advancing our
fundamental understanding of chromosome biology, these studies also open up new
avenues for studying certain diseases, such as genetic disorders that are due
to mutations in the DNA sequence which disrupt the proper activity of certain
genes. Sometimes the mutation causing these defects is not directly in the
gene, but affects one of its regulatory elements somewhere in its extended
chromosomal neighborhood.
Finding such mutations along
the chromosome has been a bit like looking for a needle in a haystack because
scientists did not know which genes were partnered with which regulatory
elements.
The hunt for such mutations
can now be directed first to the chromosomal region most likely to harbor the
regulatory elements of the misbehaving gene - inside the chromosome
"yarn" to which that gene belongs.
No comments:
Post a Comment