BIOL207 Lecture Notes - Lecture 14: Gene Mapping, Genetic Marker, Oogenesis
Document Summary
Crossover happens in almost all meiosis processes. Crossovers are detectable if one of the parents are heterozygous for 2+ gene: coupling configuration. Dominant alleles beside one another: repulsion configuration. Crossovers can be quantified w/ test cross: crossed w/ [ab/ab] for autosomal, crossed w/ [ab/y] for sex-linked (on x-chromosome) Human chr # 12: spermatogenesis crossover frequency is less than oogenesis. The gene map for human chromosome 12 is larger for females than it is for males: the frequency of crossovers occurring is proportional to the length of the gene map. If two genes are 70mu apart, the rf is 50% not 70% Genetic marker = detectable mutation of a known gene. Gene mapping via several two-point test crosses. We know that the rf between m and a is 50% (given: so we know that it is either on the same chromosome but. 50+ mu away or on the second chromosome.