Transcript Chapter 14.
Beyond Mendel’s Laws
of Inheritance
AP Biology
2006-2007
Sex linked traits
1910 | 1933
Genes are on sex chromosomes
as opposed to autosomal chromosomes
first discovered by T.H. Morgan at Columbia U.
Drosophila breeding
good genetic subject
prolific
2 week generations
4 pairs of chromosomes
XX=female, XY=male
AP Biology
Discovery of sex linkage
P
F1
true-breeding
red-eye female
X
true-breeding
white-eye male
100%
red eye offspring
Huh!
Sex matters?!
generation
(hybrids)
F2
generation
AP Biology
100%
red-eye female
50% red-eye male
50% white eye male
Genetics of Sex
In humans & other mammals, there are 2
sex chromosomes: X & Y
2 X chromosomes
develop as a female: XX
gene redundancy,
like autosomal chromosomes
an X & Y chromosome
X
Y
X
XX
XY
X
XX
XY
develop as a male: XY
no redundancy
AP Biology
50% female : 50% male
Morgan’s flies…
x
XR XR
Xr
XR
XR
AP Biology
XR Xr
XR Xr
x
XrY
XR Xr
Y
XRY
XRY
100% red eyes
XR
Xr
XRY
XR
Y
XR XR
XRY
XR Xr
X rY
100% red females
50% red males; 50% white males
Genes on sex chromosomes
Y chromosome
few genes other than SRY
sex-determining region
master regulator for maleness
turns on genes for production of male hormones
X chromosome
traits other than sex determination
mutations: (all are recessive)
hemophilia
Duchenne muscular dystrophy
color-blindness
AP Biology
sex-linked recessive
Hemophilia
H Xh x X
HY
HH
XHh
XH
female / eggs
male / sperm
XH
XH
Y
XH XH
XH Y
XH Xh
Xh
XH
Xh
AP Biology
XH Xh
XhY
carrier
disease
XHY
Y
Sex-linked disorders
Most sex-linked disorders are found on
the X chromosome.
Boys are more affected than girls.
Duchenne muscular dystrophy
Hemophlia
Colored blindness
AP Biology
X-inactivation
Female mammals inherit 2 X chromosomes
one X becomes inactivated during
embryonic development
condenses into compact object = Barr body
which X becomes Barr body is random
patchwork trait = “mosaic”
patches of black
XH
XH Xh
tricolor cats
can only be
AP Biology
female
Xh
patches of orange
Linked Genes
Genes located near each other on the
same chromosome tend to be inherited
together.
AP Biology
Linked genes
Linked genes can be separated by
crossing over of homologous
chromosomes during prophase I of
meiosis.
These offspring are known as
recombinants or recombinant types.
AP Biology
Mapping the distance between genes
A genetic map based on recombination
frequencies is called a linkage map.
AP Biology
Errors in Meiosis
Caused by nondisjunction in meiosis I
or meiosis II.
AP Biology
Errors in Meiosis
Aneuploidy – having an abnormal
number of chromosomes
Monosomic – having a missing
chromosome
Trisomic – having one extra
chromosome.
Polyploidy – having one or more extra
sets of chromosomes
AP Biology
Alterations of chromosome structure
AP Biology
Human disorders due to chromosomal alterations
Down Syndrome (trisomy 21)
Edwards Syndrome (trisomy 18)
Patau Syndrome (Trisomy 13)
XXY – Klinefelter syndrome
XO – Turner Syndrome
XXX – no problems
XYY – no problems
Philadelphia Chromosomes
Cri du chat
AP Biology
Genomic Imprinting
Variations in phenotype depending on
whether an allele is inherited from the
male or female parents.
Happens during gamete formation and
silences a particular allele of certain
genes.
Angelman Syndrome
Prader-Willi Syndrome
AP Biology
Inheritance of organelle genes
Some organelles have small circular
DNA. These organelles reproduce
themselves and transmit their genes to
daughter organelles.
Mitochondria – organism’s inherit their
mother’s mitochondrial DNA
Chloroplasts
AP Biology