Transcript Chapter 6
Chapter 6
6.1 Chromosomes and Meiosis
Gametes have half the number of chromosomes that body
cells have.
6.1 Chromosomes and Meiosis
You have body cells and
gametes
Body cells are also called
somatic cells
Germ cells develop into
gametes
Germ cells are located in
the ovaries and testes
Gametes are sex cells: egg
and sperm
Gametes have DNA that
can be passed to offspring
6.1 Chromosomes and Meiosis
Your cells have autosomes
and sex chromosomes
Your body has 23 pairs of
chromosomes.
Homologous pairs of
chromosomes have the
same structure.
For each homologous pair,
one chromosome comes
from each parent.
6.1 Chromosomes and Meiosis
Chromosome pairs 1-22
are autosomes
Sex chromosomes, X and
Y, determine gender in
mammals
6.1 Chromosomes and Meiosis
Body cells are diploid;
gametes are haploid
Fertilization between egg
and sperm occurs in sexual
reproduction.
Diploid (2n) cells have two
copies of every
chromosome.
Body cells are diploid
Half the chromosomes
come from each parent
6.1 Chromosomes and Meiosis
Haploid (n) cells have one
copy of every
chromosome.
Gametes are haploid
Gametes have 22
autosomes and 1 sex
chromosome.
6.1 Chromosomes and Meiosis
Chromosome number must
be maintained in animals.
Many plants have more than
two copies of each
chromosome.
Mitosis and meiosis are types
of nuclear division that make
different types of cells.
Mitosis make more diploid
cells.
6.1 Chromosomes and Meiosis
Meiosis makes haploid
cells from diploid cells
Meiosis occurs in sex cells
Meiosis produces gametes
6.2 Process of Meiosis
6.2 Process of Meiosis
Cells go through two
rounds of division in
meiosis.
Meiosis reduces
chromosome number and
creates genetic diversity.
6.2 Process of Meiosis
Meiosis I and meiosis II each
have four phases, similar to
those in mitosis
Paris of homologous
chromosomes separate in
meiosis I
Homologous chromosomes
are similar but not identical
Sister chromatids divide in
meiosis II
Sister chromatids are
copies of the same
chromosome.
6.2 Process of Meiosis
Meiosis I occurs after DNA
has been replicated
Meiosis I divides
homologous
chromosomes in four
phases.
6.2 Process of Meiosis
Meiosis II divides sister
chromatids in four phases
DNA is not replicated
between meiosis I and
meiosis II.
6.2 Process of Meiosis
Meiosis differs from
mitosis in significant ways
Meiosis has two cell
divisions while mitosis has
one.
In mitosis, homologous
chromosomes never pair
up. Meiosis results in
haploid cells; mitosis
results in diploid cells.
6.2 Process of Meiosis
Haploid cells develop into mature
gametes.
Gametogenesis is the production
of gametes.
Gametogenesis differs between
females and males.
Sperm primarily contribute DNA to
an embryo.
Sperm become streamlined and
motile.
Eggs contribute DNA, cytoplasm,
and organelles to an embryo.
During meiosis, the egg gets most
of the contents; the other cells form
polar bodies.
6.3 Mendel and Heredity
6.3 Mendel and Heredity
Mendel laid the groundwork
for genetics.
Traits are distinguishing
characteristics that are
inherited.
Genetics is the study of
biological inheritance
patterns and variation.
Gregor Mendel showed that
traits are inherited as discrete
units.
Many in Mendel’s day
thought traits were blended.
6.3 Mendel and Heredity
Mendel’s data revealed
patterns of inheritance.
Mendel made three key
decisions in his
experiments.
use of purebred plants
control over breeding
observation of seven
“either-or” traits
6.3 Mendel and Heredity
Mendel used pollen to
fertilize selected pea
plants.
P generation crossed to
produce F1 generation
interrupted the selfpollination process by
removing male flower
parts
Mendel controlled the
He then fertilized the female
fertilization of his pea plantspart, or pistil, with pollen from
by removing the male parts, a different pea plant.
or stamens.
6.3 Mendel and Heredity
Mendel allowed the
resulting plants to selfpollinate.
– Among the F1
generation, all plants
had purple flowers
– F1 plants are all
heterozygous
– Among the F2
generation, some plants
had purple flowers and
some had white
6.3 Mendel and Heredity
6.3 Mendel and Heredity
Mendel observed
patterns in the first and
second generations of
his crosses.
6.3 Mendel and Heredity
6.3 Mendel and Heredity
Mendel drew three
important conclusions.
– Traits are inherited as
purple
white
discrete units.
– Organisms inherit two
copies of each gene, one
from each parent.
– The two copies
segregate
during gamete formation.
– The last two conclusions
are
called the law of
segregation.
6.4 Traits, Genes and Alleles
6.4 Traits, Genes, and Alleles
The same gene can have
many versions.
A gene is a piece of DNA
that directs a cell to make
a certain protein.
Each gene has a locus, a
specific position on a pair
of homologous
chromosomes.
6.4 Traits, Genes, and Alleles
An allele is any alternative
form of a gene occurring at a
specific locus on a
chromosome.
Each parent donates one
allele for every gene.
Homologous describes two
alleles that are the same at
a specific locus.
Heterozygous describes
two alleles that are
different at a specific locus.
Traits, Genes, and Alleles
Genes influence the
development of traits
All of an organism’s
genetic material is called
the genome.
A genotype refers to the
makeup of a specific set of
genes.
A phenotype is the
physical expression of a
trait.
6.4 Traits, Genes, and Alleles
Alleles can be represented
using letters.
A dominant allele is
expressed as a phenotype
when at least one allele is
dominant.
A recessive allele is
expressed as a phenotype
only when two copies are
present.
Dominant alleles are
represented by uppercase
letters; recessive alleles by
lowercase letters.
6.4 Traits, Genes, and Alleles
Both homozygous
dominant and
heterozygous genotypes
yield a dominant
phenotype.
Most traits occur in a range
and do not follow simple
dominant-recessive
patterns.
6.5 Traits and Probability
Punnett squares illustrate
genetic crosses
The Punnett square is a grid
system for predicting all
possible genotypes resulting
from a cross.
The axes represent
the possible gametes
of each parent.
The boxes show the
possible genotypes
of the offspring.
The Punnett square yields
the ratio of possible
genotypes and phenotypes.
6.5 Traits and Probability
A monohybrid cross
involves one trait.
Monohybrid crosses
examine the inheritance of
only one specific trait.
homozygous dominant-
homozygous recessive: all
heterozygous, all
dominant
6.5 Traits and Probability
– heterozygous-
heterozygous—1:2:1
homozygous dominant:
heterozygous:
homozygous recessive;
3:1 dominant: recessive
6.5 Traits and Probability
•
heterozygoushomozygous recessive—
1:1 heterozygous:
homozygous recessive;
1:1 dominant: recessive
• A testcross is a cross
between an organism
with an unknown
genotype and an
organism with the
recessive phenotype.
6.5 Traits and Probability
A dihybrid cross involves two
triats
Mendel’s dihybrid crosses
with heterozygous plants
yielded a 9:3:3:1 phenotypic
ratio.
Mendel’s dihybrid crosses
led to his second law,
the law of independent
assortment.
The law of independent
assortment states that
allele pairs separate
independently of each
other during meiosis.
6.5 Traits and Probability
Heredity patterns can be
calculated with probability.
Probability is the likelihood
that something will happen.
Probability predicts an
average number of
occurrences, not an exact
number of occurrences.
Probability applies to random
events such as meiosis and
fertilization.
Record equation on board.
6.6 Meiosis and Genetic Variation
Sexual reproduction creates
unique combinations of
genes.
Sexual reproduction creates
unique combination of genes.
independent assortment of
chromosomes in meiosis
random fertilization of
gametes
Unique phenotypes may give
a reproductive advantage to
some organisms.
6.6 Meiosis and Genetic Variation
Crossing over during
meiosis increases genetic
diversity.
Crossing over is the
exchange of chromosome
segments between
homologous
chromosomes.
occurs during prophase I
of meiosis I
results in new
combinations of genes
6.6 Meiosis and Genetic Variation
Chromosomes contain many
genes.
The farther apart two genes
are located on a
chromosome, the more likely
they are to be separated by
crossing over.
Genes located close
together on a chromosome
tend to be inherited together,
which is called genetic
linkage.
Genetic linkage allows the
distance between two genes
to be calculated.
6.6 Meiosis and Genetic Variation