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.