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Human Heredity and Biotechnolo gy Chapter 11.1 & 11.3 with a scattering from Chapter 13

Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

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Page 1: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Human Heredity and BiotechnologyChapter 11.1 & 11.3

with a scattering from Chapter 13

Page 2: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Recessive Genetic Disorders

• Began with the study of alkaptonuria

• Passed like any recessive trait

• Heterozygous condition results in ‘carriers’

• Disorder Table: cystic fibrosis & albinism

• Disorder Table: galactosemia &Tay Sachs

Page 3: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Dominant Genetic Disorders

• Only need one dominant allele to inherit the disease

• No carriers

• Disorder Table: Huntington’s Disease & Achondroplasia

Page 4: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

PEDIGREE

chart which shows theinheritance of a trait from one generation

to the next

Allows geneticists to trace the transmission of a trait through a family.

square = malecircle = female

colored shape = has traithalf colored shape = carrier

slash = deceased

Page 5: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Alexandrina Victoria, born May 1819British Monarch

Queen Victoria was a carrier of hemophilia.

She had nine children and passed hemophilia on to several of them.

All of her children married into the royal families of various countries of Europe.

In this way, all of the Royal Families of Europe inherited the gene for hemophilia.

Page 6: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13
Page 7: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

How many generations are represented?How many males? afflicted males? normal males?

How many females? afflicted females? normal females?Any carriers?

Sex-linked or autosomal trait?Dominant or recessive trait?

Any twins? deceased individuals?

Page 8: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

HUMAN CHROMOSOMES

Humans contain….

46 individual chromosomes

23 chromosome pairs

SEX CHROMOSOMES (1 pair)

• determine the sex

of an individual

AUTOSOMES (22 pairs)

• do not determine the sex

of an individual

Page 9: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

KARYOTYPE

is a photomicrograph of the chromosomes

in a dividing cell

chromosomes are grouped

and placed into pairs

female - 46 XX

male - 46 XY

Page 10: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Telomeresprotective caps on ends on chromosomes

made of protein and DNAmay play a role in cancer and aging

Page 11: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Mutations

• Caused by mutagens (anything that may cause a mutation)

– Virus, chemicals, toxins, UV light, etc.

• 3 types1. Somatic cell mutations: affect body cells

will affect individual, but not offspring

2. Germ cell mutations: affect germ cells Will affect offspring, but not the individual

3. Lethal mutations Will cause death either before or shortly after birth

Page 12: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Chromosome Mutations

• Deletion– A piece of a chromosome is lost

• Inversion– A piece of a chromosome breaks off, flips over, and reattaches

• Translocation– A piece of a chromosome breaks off and reattaches to another

chromosome

• Nondisjunction– Homologues do not separate

Page 13: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Deletion

Page 14: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Inversion

Page 15: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Translocation

Page 16: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

NONDISJUNCTION

may arise when chromosomes don’t separate

properly during meiosis, this is called

“not coming apart”

Page 17: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Nondisjunction

• Leads to either monosomy (45) or trisomy (47) in a cell• Trisomy on #21 = Down’s Syndrome• Trisomy on sex chromosomes (#23) can lead to XXY

(Klinefelter’s syndrome) or XYY• Monosomy on sex chromosomes (#23) can lead to XO

(Turner’s Syndrome)

Page 18: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

DOWN SYNDROME(also called trisomy 21)

male or female having an extra chromosome in pair #21

(instead of 2 chromosomes in pair there are 3)

47 XX or 47 XY

Page 19: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Nondisjunction on #21 = Trisomy 21 (Down Syndrome)

Page 20: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

TURNER SYNDROME female that is missing a sex chromosome -

45 XO

Page 21: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

KLINEFELTER SYNDROME

male having an extra sex chromosome

47 XXY or 48 XXXY

Page 22: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Which mutations are shown?

Page 23: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Fetal Testing

• Genetic testing for couples with family history of genetic diseases– pre-pregnancy: DNA testing & genetic counseling– post-pregnancy: PKU testing– during pregnancy:

• Amniocentesis

• Chorionic villi sampling

• Fetal blood sampling

Page 24: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

HUMAN GENOME PROJECT

Began in 1990 -

an attempt to sequence

all of the human DNA.

Genome = an organism’s DNA

Mapping of the human

genome completed in 2003.

Page 25: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

GENE THERAPY

process in which an absent or faulty gene is replaced by a normal, working gene

various approaches have been taken…

– Bone marrow removed, modified in the laboratory and placed back in the body

– Modified viruses have been used to carry replacement genes into the body

– Inhalation of genetically engineered viruses containing “good” genes has been attempted

up to this point, gene therapy has not been very successful

Page 26: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Manipulating DNA…• Today, we have expanded our use of genetic

information and we are able to use techniques for manipulating (modifying) DNA.

We can…. • extract DNA from cells, • cut it into small pieces, • identify the genes and sequences in DNA• make copies

Page 27: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Cell Transformation….process by which a cell takes in DNA from an

outside source

• the external DNA may become part

of the cell’s DNA

Page 28: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13
Page 29: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Recombinant DNA – taking DNA from one organism and combining it with another organism

• we have inserted the genes for human insulin and human growth hormone into bacteria

Page 30: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Transgenic Organism…an organism containing genes from

another organism

cow containing genes

for producing

human milk proteins

bacterium containing

recombinant DNA

Page 31: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Cloning…process of producing an identical copy of an organism

• we have successfully cloned frogs, salamanders, mice, sheep and other organisms

Page 32: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

DOLLY

Page 33: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

What is genetic engineering?it is simply….

genetic modification

Throughout the ages,

man has applied his knowledge

of genetics to the world around him –

especially to plants and animals.

Page 34: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Selective Breeding…the process of breeding animals or plants with

desired characteristics

• Man has used selective breeding to develop plants and animals with “desirable traits”.

• Nearly all domestic animals – dogs, cats, horses, and most crop plants have been produced by selective breeding.

Page 35: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Selective Breeding…of plants

Page 36: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Selective Breeding…of animals

Page 37: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Hybridization…

crossing dissimilar individuals to bring together the best traits of both organisms

hybrids (produced by

such crosses) are

often healthier and

hardier than either

of the parents

Page 38: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Hybridization …

ZEDONK – cross between a zebra and a donkey

Page 39: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Hybridization …

LIGER – cross between a lion and a tiger

Page 40: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Hybridization …

male DONKEY and female HORSE = MULE

Offspring (mules) are almost always sterile. The mule has

greater endurance, is stronger and less excitable than a horse.

Page 41: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Inbreeding…continued breeding of individuals with similar characteristics - used to maintain

characteristics in a breed

Page 42: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

Inbreeding…

Page 43: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13

While selective breeding often limits variation, scientists are also interested in preserving the genetic diversity in organisms.

WHY?

Genetic diversity (variation) in a population

can be increased by inducing mutations.

Mutations may be induced by the

use of chemicals and radiation.

Page 44: Human Heredity and Biotechnology Chapter 11.1 & 11.3 with a scattering from Chapter 13