Notes – Ch. 15.1-15.3 Key Vocab. Wild type Mutant Recombination Recombinant Parental Genomic imprinting Recombination Frequency crossing over independent assortment linked genes linkage map X inactivation Barr body nondisjunction aneuploidy deletion insertion duplication translocation trisomy monosomy Chromosomal Inheritance – Bridge between Ch. 13 and 14 – explains the relationship between meiosis and Mendelian inheritance Meiosis Mendelian genetics Chromosomal Basis of Inheritance Morgan’s studies: White eyed male (mutant) X red eyed female (wild type) F1 = all red eyed flies (male and female) F2 = 3:1 phenotypic ratio – but only males demonstrated the white eyed mutation shows connection between sex and other traits Shows that not ALL traits assort independently from one another Supports chromosomal theory of inheritance – sex inherited WITH another trait Morgan continued his research to observe the inheritance of two traits at the same time – higher proportions of parental phenotypes than would be expected with independent assortment – so they must be inherited together Supports chromosomal theory of inheritance – traits on the same chromosome may be inherited together linked genes tend to be inherited together because they are located near each other on the same chromosome they are not ALWAYS inherited together – RECOMBINATION can still occur due to crossing over Recombination: Mixes parental genetic info – produces recombinants. A recombinant refers to offspring whose phenotype differs from either parent crossing over accounts for the recombination of linked genes o the closer two genes are to one another on a chromosome, the lower the recombination frequency & the more likely they are to be inherited together o the farther apart two genes are from one another on a chromosome, the greater the recombination frequency and the less likely they are to have linked inheritance o Recombination frequency – the percent (%) of recombinant offspring How to find the recombination frequency: Number of recombinants --------------------------------Total number of offspring X 100 Sturtevant expanded on the work of Morgan and used recombination frequencies to create linkage maps of chromosomes. helped to determine the relative locations of genes – the location of one gene relative to others - based on recombination frequencies Sex linked genes Genes present on the sex chromosomes will be inherited in conjunction with sex and display their own distinct patterns of inheritance. we are most familiar with the X-Y sex inheritance that occurs in humans and other mammals other systems exist (XX-X, Z-W, haploid-diploid) – I wouldn’t expect to see these on the AP exam Inheritance of affected X chromosomes in mammals For each of the following crosses, create a Punnett square showing inheritance and the offspring that are affected, are carriers, or are totally normal. Normal Mom X affected dad (XAXA x XaY) Carrier Mom X normal dad (XAXa x XAY) Carrier Mom X affected dad (XAXa x XaY) X Inactivation – in female mammals, X inactivation occurs early in embryonic development. This random process ensure only one X chromosome is active in each somatic cell – which can cause a mosaic phenotype (some cells express one X, other cells express the other.) This process keeps the transcriptional products of genes on the X chromosome equal to what would be produced by males who have only one X chromosome.