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(1)

Warm up

1. Why do many scientists classify viruses

as non-living?

2. Draw the basic structure of a virus.

(2)

Warm up

1. Draw the lytic/lysogenic cycle

2. What stage of the lytic-lysogenic

cycle is a virus virulent? Temperate?

(3)

Warmup

1. Define conjugation, transduction and

transformation

2. Draw and label the lac operon. Explain

(4)

CH 18-19

(5)

Microbial Models

Microbes make great models for genetics due to their simplicity, fast growth and accessibility.

Hepatitis Virus

(6)

BACTERIA

VIRUS

Both have DNA or RNA and proteins

 Prokaryotic cell

 Few are parasitic;

most free living

 Relatively large

 Many cured by

antibiotics; some are resistant

 Nucleic acid

surrounded by capsid

 Intracellular parasite

 1/1000 size of

bacteria

 Infection=Prevention

by vaccine

 NO CURES some

(7)

Process of Science: Discovery of viruses

Researchers discovered viruses by studying a plant disease - Tobacco Mosaic Virus

The small size of the TMV

(8)

A virus = nucleic acid of DNA or RNA enclosed in a

protective protein capsid & sometimes a membraneous

(9)

How to be a Virus

Invader

Viruses can reproduce only within a host cell

The viral genome is inserted into the cell along with enzymes.

The cells DNA is broken up. The cell begins to copy the viral genome and reads it to make viral proteins

(10)
(11)
(12)

Animal viruses are

diverse in their modes of infection and

replication

Researchers ask:

1. Does it have DNA or RNA

2. Is it double stranded

(DS)or single stranded (SS) 3. Does it have an

(13)

Enveloped viruses have different

methods of lytic reproduction in animal cells.

The membraneous envelope comes from the host cell, forming around

them as they exit. This envelope

makes it hard for a host’s immune

(14)

Proviruses replicate in the host’s nucleus. These viruses have an envelope that comes from a host’s nuclear membranes.

The viral genome can join with the hosts DNA, in a lysogenic fashion. This lets the virus lie

dormant for long periods of time, emerging from time to time

Herpes is a provirus.

Provirus=

eukaryote host

Prophage=

(15)

Retro viruses use an RNA genome

Retro viruses use an enzyme called

reverse transcriptase

that turns their RNA into DNA.

Retro viruses insert into the host’s DNA and can lie dormant for years before

beginning a

(16)

Retro viruses use an RNA genome

HIV is a retrovirus.

HIV+ means the virus is in your DNA.

AIDS means the

(17)
(18)

Other Human Viruses

(19)

New Emerging Human Viruses

Ebola Viruses Hanta Viruses

New viruses can mutate from an old one. RNA viruses, like flu, mutate often. They can also

(20)

Viroids

 Circular RNA molecules,

several hundred nucleotides in length

 Infects plants

 Cause errors in regulatory

systems that control plant growth

 Eg. coconut palms in

(21)

Prions

 Midfolded, infectious proteins that cause

misfolding of normal proteins

 Causes degenerative brain diseases in animals

(spongiform encephalopathy)

 Eg. scrapie (sheep), mad cow disease (BSE),

(22)

Diseases caused by prions

 Prions act slowly – incubation period of at least

10 years before symptoms develop

 Prions are virtually indestructible (cannot be

denatured by heating)

(23)

How prions propagate

(24)

The Genetics of Bacteria

Bacteria evolve quickly due to their short

reproductive cycle,

mutations and genetic recombination

Binary Fission-begins at origin and copies in both directions

(25)

Bacterial Reproduction

Bacteria exchange DNA in several ways:

Transduction

(26)

Transformation

bacteria takes up naked, foreign DNA from

surrounding environment

(27)

Transduction

Transduction uses

viruses to move DNA from cell to cell

When the new virus invades a new cell,

the bacterial fragment recombines with the host’s DNA.

Specialized

transduction involves lysogenic viruses.

When the virus starts a lytic cycle it

(28)

Conjugation

Conjugation= joining two

bacteria with a tube called a sex pili.

Only smaller round DNA

genomes called

(29)

Conjugation

The ability to form a sex pili (male) is carried on an F plasmid. F stands for fertile.

Here an F plasmid is transferred to another bacteria. It will now be able to make sex pili as well.

Plasmids act as supplemental DNA sources. They replicate along with the main

(30)

Conjugation

A plasmid can also be incorporated into the main chromosome. This makes an Hfr cell,

which stands for high frequency of recombination

(31)

Conjugation

Here an F plasmid is transferred to another bacteria by an Hfr cell. Only portions of the entire chromosome transfer before the sex pili disconnects.

(32)

There are many plasmids in the bacterial

world. Some can carry genes for resistance to antibiotics. Plasmids that carry these

resistances are R plasmids.

Some R plasmids can carry resistance for up to ten

different antibiotics.

(33)

Transposons: transposable genetic

elements or “jumping genes”; genes that have no permanent location and move

from place to place

(34)

Transposons

 Transposase: enzyme that catalyzes movement

within genome

 Transposons include extra genes such as

antibiotic resistance

(35)

Control of Gene Expression

Negative

feedback by the end products of biochemical

pathways can

(36)

Operons

This is the trp operon. It contains the genes to manufacture the amino acid trytophan- if it is not available.

(37)

Operons

Between the promoter and the genes is a special site called the operator-the on/off switch that can block RNA polymerase

The operon contains a promoter site for RNA

(38)

Repressible Operons

The gene will be transcribed and translated and tryptophan will be made.

Trp is a repressible operon - it is always on

(39)

Repressible Operons

The active repressor now binds to the operator and shuts down the trp operon. This is negative feedback by the end product trytophan.

(40)

Inducible operons

This is the lac operon, which makes enzymes to metabolize the sugar lactose.

(41)

If glucose supplies fall, and lactose is present then this operon gets switched on.

Cells prefer to metabolize glucose. So this

(42)

Inducible operons

Without cAMP, the initiation factor can not bind, and neither can RNA polymerase. This operon shuts down when both sugars are present.

(43)

Warm up

 1. How is DNA packaged into Chromosomes?

 2. What are pseudogenes?

 3. Contrast DNA methylation to histone

(44)

Warm up

 1. Why are transposons important in genetics?

 2. How and why do cells differentiate?

(45)

Control of Eukaryotic Genome-ch19

Eukaryotic

chromosomes are much more complex

than the single

circular chromosome found in prokaryotes.

These chromosomes are made of DNA and a complex of proteins. This material is called

(46)

Chromatin structure

is based on levels of DNA packing.

1. Protein histones wind DNA into

nucleosome beads 2. Nucleosome

beads coil and fold up with the help of other

proteins that act as scaffolds

(47)

Genome Organization at the DNA Level Tandem DNA=

repeating short patterns of DNA nucleotides;

has a different density than

regular DNA and forms a “satellite” bands when

centrifuged.

Fragile X is a

mutation where an

(48)

Gene families have evolved by duplication of ancestral genes

Hemoglobin is a protein with quaternary

structure.

Made of four globular proteins These duplicated genes are called multigene families

There are many repeats of this

protein in human DNA, similar but not identical. They turn on and off at different times. They can all be traced back to an individual

(49)

Gene amplification can add extra sources of

mRNA when needed, as in a developing embryo. Re-arrangement can alter a cell's genome

A transposon can knock out a gene by copying into its middle, or turn one on or off

(50)

The Control of Gene Expression

Each eukaryotic cell

expresses only a small fraction of its genes.

Differentiation determines which genes turn on and off as an embryo develops.

The control of gene

expression can occur at any step in the pathway from

(51)

Chromatin modifications= affect the availability of genes for transcription. Epigenetic changes do not affect the sequence of the code, only the reading of the code

DNA methylation = deactivates sections of a chromosome (Barr bodies in females);

(52)

A Eukaryotic Gene

Transcription initiation is controlled by

transcription factors. These factors bind to the

(53)

Control of Transcription Initiation

Close to the promoter are control elements, and another set of control elements called enhancers

(54)

Activators attach to the enhancers. Together with initiation factors that binds to the TATA end of a promoter, a site for RNA polymerase binding forms.

The DNA bends and helps hold together the transcription factors. This creates a

transcription

initiation complex

(55)

.

Processing of mRNA introns and exons in different ways can control protein production, especially by adding regulatory sites.

(56)

The Molecular Biology of Cancer

Cancer results from genetic changes that affect the cell cycle. Proto-oncogenes promote normal cell growth.

(57)

Oncogene proteins with faulty tumor-suppressor

proteins can interfere with normal signaling pathways.

The ras protein plays a vital role in controlling cell growth. If it is

transformed into a

hyperactive state, cell growth is

overstimulated .

An initiation factor called

(58)

Multiple mutations underlie the development of cancer

Combinations of the loss of tumor supressors with the addition of hyperactive oncogenes

References

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