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Chapter 18~ Microbial Models: The Genetics of Viruses and Bacteria

Chapter 18~ Microbial Models: The Genetics of Viruses and Bacteria

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Chapter 18~ Microbial Models: The Genetics of Viruses and Bacteria. Viral structure. Virus: “ poison ” (Latin); infectious particles consisting of a nucleic acid in a protein coat Capsid; (viral envelopes); DNA or RNA Bacteriophages (phages). Viral reproduction: Lytic Cycle. - PowerPoint PPT Presentation

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Page 1: Chapter 18~ Microbial Models:  The Genetics of Viruses and Bacteria

Chapter 18~Microbial Models: The Genetics of Viruses and Bacteria

Page 2: Chapter 18~ Microbial Models:  The Genetics of Viruses and Bacteria

Viral structure

Virus: “poison” (Latin); infectious particles consisting of a nucleic acid in a protein coat

Capsid; (viral envelopes); DNA or RNA

Bacteriophages (phages)

Page 3: Chapter 18~ Microbial Models:  The Genetics of Viruses and Bacteria

Viral reproduction: Lytic Cycle

Host range: infection of a limited range of host cells (receptor molecules on the surface of cells)

The lytic cycle: 1- attachment 2- injection 3-hydrolyzation 4- assembly 5- release Results in death of host cell Virulent virus (phage

reproduction only by the lytic cycle)

Page 4: Chapter 18~ Microbial Models:  The Genetics of Viruses and Bacteria

Viral reproduction: Lysogenic Cycle

Genome replicated w/o destroying the host cell

Genetic material of virus becomes incorporated into the host cell DNA (prophage DNA)

Temperate virus (phages capable of using the lytic and lysogenic cycles)

May give rise to lytic cycle

Page 5: Chapter 18~ Microbial Models:  The Genetics of Viruses and Bacteria

RNA viruses

Retroviruses: transcribe DNA from an RNA template (RNA--->DNA)

Reverse transcriptase (catalyzing enzyme)

HIV--->AIDS

Page 7: Chapter 18~ Microbial Models:  The Genetics of Viruses and Bacteria

Viroids and prions

Viroids: tiny, naked circular RNA that infect plants; do not code for proteins, but use cellular enzymes to reproduce; stunt plant growth

Prions: “infectious proteins”; “mad cow disease”; trigger chain reaction conversions; a transmissible protein

Page 8: Chapter 18~ Microbial Models:  The Genetics of Viruses and Bacteria

Bacterial genetics Nucleoid:

region in bacterium densely packed with DNA (no membrane)

– DNA is circular Plasmids:

small circles of DNA Reproduction:

binary fission (asexual)

Page 9: Chapter 18~ Microbial Models:  The Genetics of Viruses and Bacteria

Bacterial DNA-transfer processes

Transformation: genotype alteration by the uptake of naked, foreign DNA from the environment (Griffith expt.)

Transduction: phages that carry bacterial genes from 1 host cell to another

– •generalized~ random transfer of host cell chromosome

– •specialized~ incorporation of prophage DNA into host chromosome

Conjugation: direct transfer of genetic material; cytoplasmic bridges; pili; sexual

Page 10: Chapter 18~ Microbial Models:  The Genetics of Viruses and Bacteria

Bacterial Plasmids Small, circular, self-replicating DNA separate from the bacterial

chromosome F (fertility) Plasmid: codes for the production of sex pili (F+ or F-) R (resistance) Plasmid: codes for antibiotic drug resistance Transposons: transposable genetic element; piece of DNA that can move

from location to another in a cell’s genome (chromosome to plasmid, plasmid to plasmid, etc.); “jumping genes”

Page 11: Chapter 18~ Microbial Models:  The Genetics of Viruses and Bacteria

Operons: Type I Repressible (trp operon): tryptophan (a.a.) synthesis promoter: RNA polymerase binding

site; begins transcription operator: controls access of RNA

polymerase to genes (tryptophan not present)

repressor: protein that binds to operator and prevents attachment of RNA polymerase ~ coded from a regulatory gene (tryptophan present ~ acts as a corepressor)

transcription is repressed when tryptophan binds to a regulatory protein

Def: Unit of genetic function consisting of coordinately related clusters of genes with related functions (transcription unit)

Page 12: Chapter 18~ Microbial Models:  The Genetics of Viruses and Bacteria

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Page 13: Chapter 18~ Microbial Models:  The Genetics of Viruses and Bacteria

Operons: Type II

Inducible (lac operon): lactose metabolism lactose not present:

repressor active, operon off; no transcription for lactose

enzymes lactose present: repressor

inactive, operon on; inducer molecule inactivates protein repressor (allolactose)

Transcription is stimulated when inducer binds to a regulatory protein

Def: Unit of genetic function consisting of coordinately related clusters of genes with related functions (transcription unit)

Page 14: Chapter 18~ Microbial Models:  The Genetics of Viruses and Bacteria

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Page 15: Chapter 18~ Microbial Models:  The Genetics of Viruses and Bacteria

19.1-Chromatin Structure in Eukaryotic Genomes

Chromatin - complex of DNA and proteins

Page 16: Chapter 18~ Microbial Models:  The Genetics of Viruses and Bacteria

Histone protein – + charged amino acids binds to – - charged phosphates of DNA

Nucleosome – - DNA wrapped around the histone– - “beads on a string”– - basic unit of DNA packing

Heterochromatin•highly condensed interphase DNA

(can not be transcribed) Euchromatin

•less compacted interphase DNA (can be transcribed)

DNA Packing or Organization

Page 17: Chapter 18~ Microbial Models:  The Genetics of Viruses and Bacteria

Molecular Biology of Cancer Oncogene •cancer-

causing genes

Proto-oncogene •normal cellular genes

How?

1-movement of DNA; chromosome fragments that have rejoined incorrectly

2-amplification; increases the number of copies of proto-oncogenes

3-proto-oncogene point mutation; protein product more active or more resistant to degradation

Tumor-suppressor genes •changes in genes that prevent uncontrolled cell growth (cancer growth stimulated by the absence of suppression)

Page 18: Chapter 18~ Microbial Models:  The Genetics of Viruses and Bacteria

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RNAi Discussion - Nova online

How can turning individual genes off help scientists better understand normal growth and development?

Some diseases involve an overproduction of proteins or the production of defective proteins. How might RNAi be used to control the overproduction of proteins or eliminate the production of defective proteins, thereby helping cure or control such diseases.

Which genetic diseases might not be able to be helped by RNAi? 1

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