The Chromosomal Basis of Mendels Laws Mendels principle

The Chromosomal Basis of Mendel’s Laws

Mendel’s “principle of segregation” a. pairs of genes on homologous chromosomes separate during gamete formation (meiosis) and end up in different gametes. b. the fusion of gametes at fertilization pairs genes once again. Ex: The alleles for height in Mendel’s pea plants end up in separate gametes. Tt X Tt could yield four the offspring: TT, Tt, tt.

• Mendel’s “principle of independent assortment” a. each pair of alleles on nonhomologous chromosomes segregates independently of other pairs during gamete formation Ex: When Mendel crossed F 1 plants that were heterozygous for round yellow peas, some F 2 plants did not resemble the parent plants.

Morgan’s First Mutant

Sex-linked Inheritance w+ = red w = white

Drosophila Testcross Black and Vestigial Wild Type (Gray and Normal) Gray and Normal Black and Vestigial

Evidence for linked genes in Drosophila Non-Parental Phenotype

Recombination Due to Crossing Over

If the two genes were on different chromosomes, the alleles from the F 1 dihybrid would sort into gametes independently, and we would expect to see equal numbers of the four types of offspring. Since most offspring had a parental phenotype it can be concluded that the genes for body color and wing size are located on the same chromosome.

Linked genes tend to be inherited together because they are located near each other on the same chromosome. Recombinants have different phenotypes than the parents.

Morgan, who discovered that genes were located on chromosomes, proposed that some process must occasionally break the physical connection between genes on the same chromosome. This is now called crossing over, which accounts for the recombination of linked genes.

Sturdevant, a student of Morgan’s, devised a way to construct genetic maps, an ordered list of the genetic loci along a particular chromosome. He predicted that the further apart two genes are on a chromosome, the higher the probability that crossing over will occur.

Using recombination frequencies to construct a genetic map a second crossover would cancel out the first and reduce the observed b-vg recomb. frequency 1 map unit is equal to 1% recombination frequency

A genetic map based on recombination frequencies is called a linkage map and is based on the assumption that the probability of a crossover between two genetic loci is based on the distance separating the loci. The distances between genes are expressed as map units, with one map uni equivalent to a 1% recombination frequency.

Partial Genetic Map of a Drosophila Chromosome The numbers represent the distance between that locus and the locus for aristae length.

Investigators performed crosses that indicated bar-eye and garnet-eye alleles are 13 map units apart, scallop -wing and bar-eye alleles are 6 units apart, and garnet-eye and scallop-wing alleles are 7 units apart. What is the order of these alleles on the chromosome?

Given the following recombination frequencies, what is the correct order of the genes on the chromosome? A-B, 8 map units; A-C, 28 map units; A-D, 25 map units; B-C, 20 map units; B-D, 33 map units a)A-B-C-D d) B-A-D-C b)D-C-A-B e) D-A-B-C c)A-D-C-B

The frequency of crossing over between linked genes A and B is 35 percent; between B and C, 10 percent; between C and D, 15 percent; between C and A, 25 percent; between D and B, 25 percent. The sequence of the genes on the chromosome is: a. ACDB c. ABDC e. ADCB b. ADBC d. ABCD

Suppose alleles M and n are linked on one chromosome, and m and N are linked on the homologous chromosome. Individuals homozygous for M and n are mated with individuals homozygous for m and N. Their offspring are crossed with homozygous recessive individuals, and the following results are recorded: Mn/mn 15 m. N/mn 13 MN/mn 232 mn/mn 240 How many units apart are these genes on the chromosome?

Some Chromosomal Systems of Sex Determination Males have 1 X Sex Chromosome present in ovum Unfertilized males; fertilized females

Although female mammals, including humans, inherit two X chromosomes, one X chromosome in each cell becomes almost completely inactivated during embryonic development. The inactive X in each cell of a female condenses into a compact object called a Barr body, which lies along the inside of the nuclear envelope.