Cot Curve
Cot Curve
Cot Curve
Cot Curve
DNA transposon
12 5800 3.4
The human genome consists of all the DNA present in the cell. It can be divided into the nuclear genome (about 3200 Mbp) and the mitochondrial genome (16.6 kb). We will discuss the mitochondrial genome later. It has long been known that nuclear DNA can be divided into a unique fraction and several classes of repeated sequence DNA. This is based on Cot curve analysis.
Cot Curves
Cot curves are generated by shearing DNA to about 1000 bp length, then melting it, lowering the temp and allowing it to re-anneal, measuring the % still single stranded at various time points. The rate-limiting step is the collision of two complementary molecules, giving second-order reaction kinetics. The rate of collisions is proportional to initial concentration (Co) times time (t), or Cot. Whether a collision results in formation of a double stranded molecule depends on whether the two strands are complementary. Get a sigmoid curve which can be characterized by the Cot1/2 value, the point where 1/2 of the DNA is still single stranded.
Satellite DNA
Satellite DNA: based on DNAs behavior during density gradient (isopycnnic) centrifugation. During centrifugation at 50,000 x g, a CsCl solution settles into a gradient of density: more dense near the bottom of the tube. Objects in the solution float to their neutral buoyancy point. The bulk of human DNA forms a band at a density of 1.55. However, short tandem repeats have a slightly different density because they don't have the same base composition as bulk DNA--they form density "satellites" in the centrifuge tube, bands of slightly different density above or below the main DNA band. Three density satellites for human DNA: I, II, and III. Found in centromere regions on all chromosomes. An example: "alpha" (or alphoid) sequence is 171 bp repeat found at all centromeres in many copies. It apparently binds the kinetochore proteins (which anchor the spindle fibers). Lots of variation between chromosomes, and the variants seem to evolve rapidly.
DNA transposons move by cutting out the DNA sequence of the element and inserting it in a new location (usually). Another important distinction: autonomous transposons can move independently: they code for the enzymes necessary for transposition. Non-autonomous elements rely on enzymes produced by autonomous elements elsewhere in the genome.