Genetic recombination allows determination of the distance between genes on chromosomes.
Mapping chromosomes can pinpoint exact gene locations.
Homologous Chromosomes: A pair of chromosomes from different parents (e.g., orange/paternal and yellow/maternal).
Sister Chromatids: Identical chromatids on the same chromosome, carrying identical genes.
Chromosomes appear as X shapes following replication, consisting of two sister chromatids joined at a centromere.
A chromosome is counted by the number of centromeres present.
Genes are represented by colored circles on the chromatids:
Green Genes: Represent complexion traits (e.g. dark vs. light complexion).
Purple Genes: Represent hair color traits.
Blue Genes: Represent eye color traits.
Genetic recombination typically occurs between homologous chromosomes—not sister chromatids (identical).
Chromatids exchange segments of genetic material, leading to new allele combinations:
Example changes occur by swapping segments at various points (e.g., top, middle, bottom).
The proximity of genes affects the likelihood of recombination.
Gene Proximity:
Greater distances between genes increase the likelihood of recombination.
Closer genes are less likely to recombine.
Recombination is more probable between distant genes, such as purple and green genes, compared to closer genes like blue and purple genes.
Centimorgan (cM): A unit for measuring the distance between genes; also known as a map unit (m.u.).
Defined as the distance over which there is a 1% chance that recombination occurs during meiosis.
Example 1:
If two genes are 25 map units apart, recombination occurs 25% of the time (1/4).
A visualization often includes identified chromatids swapping sections to illustrate recombination.
Example 2:
If genes are 6 map units apart, recombination occurs 6% of the time (6/100).
Statistical analysis of recombination frequency can help map genes on a chromosome.
This allows for a clearer understanding of gene locations and relationships on chromosomes.