That Knotty DNA
In
this article, we'll look at one tool, the Jones polynomial, which has
been used by molecular biologists in their investigations of DNA...
David Austin
Grand Valley State University
david at merganser.math.gvsu.edu
Introduction
Gardening presents a mathematical challenge for me: As I drag the
garden hose around my lawn, the hose invariably gets tangled up with
itself in ways that can seem endlessly complicated. Untangling the
hose usually requires time and patience; the job would be a lot
easier if I could somehow pass the hose through itself to untangle
it.
Still, my garden hose is nothing compared to the complexity of DNA
in the nucleus of a cell. For example, imagine the nucleus of a cell
scaled to the size of a basketball. The DNA contained inside would
form a 200 kilometer long double-stranded filament tightly knotted
inside. Now think about what happens when a cell divides: A second
copy of the DNA is produced, which is necessarily tangled up with the
first, and this copy must somehow be pulled apart from the original.
Enzymes, known as topoisomerases, assist by breaking and rejoining
strands of DNA; in essence, topoisomerases allow the molecules to pass
through one another, just as I wish for my garden hose.
These enzymatic actions are of great interest to molecular biologists,
who have spent considerable effort exploring them experimentally. To
detect changes effected by the enzymes, however, we need some way to
compare the knottedness of two molecules. This is where mathematics
comes in.
The study of knots began in earnest in the 1860's when William
Thompson (Lord Kelvin) proposed his vortex model of the atom. Simply
said, this theory postulated that atoms were formed by knots in the
ether and that different chemical elements were formed by different
knots. Though Kelvin's theory eventually proved to be of little
physical use, it was seriously considered for long enough to lead
mathematicians to begin a detailed study of knots.
Of particular interest to mathematicians is the problem of
determining whether two knots, like the ones shown below, are the same or
different. That is, can we reconfigure one of the knots, without
cutting, so that it looks like the other?
Knots are phenomenally complicated: if we just look at knots that
appear to cross 16 times or less, we find that there are 1,388,705
different knots. Since Kelvin's time, mathematicians have developed
increasingly powerful tools for making sense of this complexity. In
this article, we'll look at one tool, the Jones polynomial, which has
been used by molecular biologists in their investigations of DNA.
Naming knots
One problem with knots is that there are many ways to look at
them; what appears complicated at first sight could simply be due to
our misfortune at having looked in the wrong way. For instance, the
two knots below are really the same though one appears, at least at
first glance, to be a more complicated knot.
To distinguish knots from one another, mathematicians have
developed ways to assign names to knots, just the way that people have
names assigned to them. Of course, people with different names are
different; in the same way, knots with different names are different
as well. In the 1980's, Vaughn Jones found a way to name knots by
associating a polynomial, now called the Jones polynomial, to every
knot. This is a particularly powerful way to name knots for it
distinguishes many knots from one another. The Jones polynomials are
shown for the knots below. As you can see, the polynomials are
different and so the knots themselves must be different.
 |
V(t)
=t+t3-t4,
|
 |
V(t)
=t2-t+1-t-1+t-2.
|
Rather surprisingly, Jones found his polynomial through his
work in operator algebras, an area of mathematics seemingly far-flung
from knot theory. In this article, we'll follow a path to the Jones
polynomial found by Louis Kauffman.
Link diagrams
Let us restate a fundamental difficulty in dealing with knots:
different pictures of the same knot may look wildly different.
However, a theorem proved by Kurt Reidemeister in the 1930's gives us
a way to understand how different pictures of the same knot may vary
from one another.
In what is coming, we will need to work with links, which are
merely collections of knots. The following three simple changes,
called Reidemeister moves, may be made to the picture of a
link without changing the link itself.
If we are given two pictures of the same link, Reidemeister's
theorem guarantees that there is a sequence of these three moves that
lead from one picture to the other. The example below illustrates:
 |
Move II |
 |
Move I |
 |
|
Move III |
 |
Move III |
 |
The Kauffman and Jones polynomials
As we'll now see, Kauffman began by associating a polynomial,
called the bracket polynomial, in variables x,
y, and z to the picture of a link. For instance,
The bracket polynomial is defined by three simple rules.
|
1.
First, we will assign a simple polynomial to the unknot:
2.
Our strategy will be to compute the polynomial by eliminating
crossings:
3.
We will also eliminate circles from the link diagrams.
If D is a diagram and one circle is added to the diagram,
then
|
Let's see how this works in the following example:
|
= x |
|
+ y |
|
|
= x2 |
|
+ xy |
|
|
+ yx |
|
+ y2 |
|
|
= (x2+y2)z |
|
+ 2xy |
|
= (x2+y2)z + 2xy |
Remember that we would like to have a polynomial that depends only
on the underlying link, rather than the diagram we are using to
represent it. This would be the case if the polynomial is unchanged
when we perform any of the three Reidemeister moves. Considering the
first Reidemeister move, we would therefore like to have
Let's see where this leads us:
|
= x |
|
+ y |
|
 |
= x2 |
|
+ xy |
|
|
+ yx |
|
+ y2 |
|
 |
= xy |
|
+ (x2+y2+xyz) |
|
Since we would like
we must have
xy = 1
x2 + y2 + xyz = 0.
In other words,
y = x-1
z = -(x2 + x-2)
Let's revise our three rules now:
With these new rules, it turns out (remarkably) that the bracket
polynomial is unchanged by the second Reidemeister move:
Now we need to check the third Reidemeister move:
|
= x |
|
+ x-1 |
|
 |
= -x(x2+x-2) |
|
+ x-1 |
|
 |
= -x3 |
|
This looks like a problem. We would like for the bracket
polynomial to be unchanged under all three Reidemeister moves. Moves
I and II leave it unchanged, but straightening out the kink in move
III introduces a factor of -x3.
Fortunately, there is a way to fix this problem. To do so, we
will first orient the link diagram by putting arrows on it:
and define the incidence number of a crossing to be:
|
+1 if the crossing is like |
 |
|
-1 if the crossing is like |
 |
The writhe of the diagram is now the sum of all the
incidence numbers. You may wish to check that the writhe of a
knot diagram does not depend on how we oriented the knot.
Notice that Reidemeister move III changes the writhe:
|
writhe |
 |
+ 1 = writhe |
 |
Therefore, if we have an oriented link diagram L and
define the polynomial PL(x) to be
|
PL(x) = (-x3)writhe(L) |
 |
L |
 |
then this polynomial depends only on the oriented link and not on
the diagram used to represent it. In other words, everyone who draws
a picture of this link will still compute the same polynomial
regardless of how his or her picture looks. Also, if L is a knot,
then the polynomial does not depend on the orientation since the
writhe is independent of the orientation.
A good exercise is to compute the polynomial for the trefoil
knot:
 |
PT(x)
=x-4+x-12-x-16,
|
or the figure 8 knot:
 |
P8(x)
=x8-x4+1-x-4+x-8.
|
This polynomial, known as the Kauffman polynomial, is related to
the Jones polynomial, which predates it. The Jones polynomial is
given by
VL(t)=PL(t -1/4)
Chirality
Molecules often occur in pairs, each of which is the mirror image
of the other, and biologists would like to distinguish between them.
The Jones polynomial is also helpful here.
Imagine looking at a link in a mirror that is directly behind the
link. We would see the same link diagram, but the over- and
under-crossings would simply be interchanged. For instance, here is a
trefoil knot and its mirror image:
Let's first consider the effect of interchanging an over- and
under-crossing on the bracket polynomial:
Also, interchanging over- and under-crossings will change the sign
of all the incidence numbers
so the writhe changes sign.
Putting these two observations together means that if
is the mirror image of the oriented link
L, then
and hence
Consider now the trefoil and its mirror image:
 |
 |
|
V(t)
=t+t3-t4
|
V(t)
=t-1+t-3-t4
|
Since the two polynomials are different, this shows that the
trefoil and its mirror image are two different knots. That is, there
is no way to deform the trefoil into its mirror image without cutting
it apart and tying it back together.
You may wonder about the figure 8 knot, since its polynomial is
V(t)
=t2-t+1-t-1+t-2
=V(t-1).
This tells us that the Jones polynomial cannot distinguish between
the figure 8 knot and its mirror image. It turns out that the figure
8 knot is equivalent to its mirror image, a fact that you may wish to
verify by finding a sequence of Reidemeister moves that takes the
picture of the figure 8 knot into its mirror image.
Summary
After Kelvin's vortex theory was abandoned as an explanation for
atomic structure, mathematicians studied knots for over a century
motivated mainly by curiosity. In some sense, Jones's work represents
the culmination of this work for it seems to bring together several
areas of mathematics. As mentioned, Jones's original motivation came
from operator algebras. In addition, the Jones polynomial
forms rather deep connections between knot theory and statistical
mechanics and quantum field theory.
Also unexpected is its usefulness in studying the chemical
processes of life. Nicholas Cozzarelli, a molecular biologist at the
University of California-Berkeley until his death last year, said:
"Before Jones, the math was incredibly arcane. The way the knots were
classified had nothing to do with biology, but now you can calculate
the things important to you".
This phenomenon is not uncommon. New mathematics is often
discovered out of simple curiosity yet is indispensable for describing
the world around us.
References
Knot theory references accessible to undergraduates.
Colin Adams, The Knot Book, American
Mathematical Society, 2004.
Charles Livingston, Knot Theory, Mathematical
Association of America, 1996.
Standard references on knot theory
Dale Rolfsen, Knots and Links, Publish or
Perish, 1976.
W.B. Raymond Lickorish, An Introduction to Knot
Theory, Graduate Texts in Mathematics, Springer, 1997.
More specific references to the Kauffman and Jones polynomials
Louis Kauffman, Knots and Physics, World
Scientific, 1991.
Vaughn Jones, "A Polynomial Invariant for Knots via von
Neumann Algebras." Bulletin of the American Mathematical
Society 12, 103-111, 1985.
Vaughn Jones, "Hecke Algebra Representations of Braid
Groups and Link Polynomials." Annals of Mathematics
126, 335-388, 1987.
Kurt Reidemeister. Knotentheorie, Springer
Verlag, 1932.
Connections between biology, chemistry and knot theory
De Witt Sumners, "Untangling DNA." Mathematical
Intelligencer 12, 71-80, 1990.
Lisa Postow, Brian Peter, Nicholas Cozzarelli, "Knot what we
thought before: the twisted story of replication."
BioEssays 21, 805-808, 1999.
Alexei Podtelezhnikov, Nicholas Cozzarelli, Alexander
Vologodskii, "Equilibrium distributions of topological state in
circular DNA: Interplay of supercoiling and knotting." Proceedings
of the National Academy of Sciences 96, 12974-12979, 1999.
Erica Flapan, When topology meets chemistry: A
topological look at molecular chirality. Cambridge
University Press, 2000.
David Austin
Grand Valley State University
david at merganser.math.gvsu.edu

NOTE: Those who can access JSTOR can find some of the
papers mentioned above there. For those with access, the American Mathematical
Society's MathSciNet can be used to get
additional bibliographic information and reviews of some these materials. Some of the
items above can be accessed via the ACM
Portal, which also provides bibliographic services.
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