CRISPR-Cas: To Take Up DNA or Not—That Is the Question

Slides:



Advertisements
Similar presentations
Griffith’s work on Pneumococcus. Frederick Griffith (1920) was a medical officer in London. He was looking for a way to fight pneumonia in the epidemics.
Advertisements

Group Reading… Each group is going to be assigned a scientist/experiment to read. Each group will need to have: 2 Readers 1 Scribe (You decide in your.
8.1 Identifying DNA as the Genetic Material
Bacterial Transformation
Hershey and Chase confirmed that DNA, and not protein, is the hereditary material.
“The Blueprint of Life”
Chapter 12 DNA: The Genetic Material Identification of the Genetic Material (DNA) In 1928, an experiment unrelated to genetics led to the discovery of.
Human Gut Microbes Use Multiple Transporters to Distinguish Vitamin B12 Analogs and Compete in the Gut Patrick H. Degnan, Natasha A. Barry, Kenny C. Mok,
The Transcription Factor Foxo1 Controls Central-Memory CD8+ T Cell Responses to Infection Myoungjoo V. Kim, Weiming Ouyang, Will Liao, Michael Q. Zhang,
Nucleocapsid Phosphorylation and RNA Helicase DDX1 Recruitment Enables Coronavirus Transition from Discontinuous to Continuous Transcription Chia-Hsin.
12-1: DNA Biology 2. In the mid 1900’s biologists wondered: How do genes work? What are they made of? How do they determine characteristics? Are they.
Genes Induced Late in Infection Increase Fitness of Vibrio cholerae after Release into the Environment Stefan Schild, Rita Tamayo, Eric J. Nelson, Firdausi.
A View to a Kill: The Bacterial Type VI Secretion System Brian T. Ho, Tao G. Dong, John J. Mekalanos Cell Host & Microbe Volume 15, Issue 1, Pages 9-21.
Cell-to-Cell Transfer of M. tuberculosis Antigens Optimizes CD4 T Cell Priming Smita Srivastava, Joel D. Ernst Cell Host & Microbe Volume 15, Issue 6,
Merkel Cell Polyomavirus Small T Antigen Controls Viral Replication and Oncoprotein Expression by Targeting the Cellular Ubiquitin Ligase SCFFbw7 Hyun.
Discovery of DNA Fredrick Griffith – 1928 Oswald Avery – 1944 Alfred Hershey & Martha Chase
Identifying the Genetic Material A.Griffith’s Experiment (1928) -Frederick Griffith was trying to find a vaccine against pneumonia. -Pneumonia is caused.
Chapter 12: DNA and RNA.
A CRISPR View of Cleavage
H. pylori GPS: Modulating Host Metabolites for Location Sensing
DNA How did we figure it out?.
Identifying the Substance of Genes (12.1)
RAS and ROS—A Story of Pseudomonas Survival
Trained Immunity: An Ancient Way of Remembering
Strength in Diversity Cell Host & Microbe
The Avian Influenza Virus Polymerase Brings ANP32A Home to Roost
Influenza Vaccines: Challenges and Solutions
Message in a Biota: Gut Microbes Signal to the Circadian Clock
Volume 9, Issue 2, Pages (August 2011)
NMD: Nonsense-Mediated Defense
Shigella Stays on the Move
Volume 20, Issue 4, Pages (October 2016)
DNA Ch. 10.
Candida albicans Adds More Weight to Iron Regulation
Autophagy, Apoptosis, and the Influenza Virus M2 Protein
Influenza A Virus PB1-F2: A Small Protein with a Big Punch
A Microbiome Foundation for the Study of Crohn’s Disease
Volume 22, Issue 2, Pages (August 2017)
Neutrophils Cause an Intravascular Traffic Jam
CRISPR Interference Can Prevent Natural Transformation and Virulence Acquisition during In Vivo Bacterial Infection  David Bikard, Asma Hatoum-Aslan,
Type VI Secretion: Not Just for Pathogenesis Anymore
Volume 22, Issue 3, Pages (September 2017)
Natural competence for transformation
Testosterone: More Than Having the Guts to Win the Tour de France
The Avian Influenza Virus Polymerase Brings ANP32A Home to Roost
Restriction of Zika Virus by Host Innate Immunity
Finding Leishmania: A Deadly Game of Hide-and-Seek
Proteins in Plant Brassinosteroid Signaling
HIV Latency Gets a New Histone Mark
Recognizing Macrophage Activation and Host Defense
A Microbiome Foundation for the Study of Crohn’s Disease
A Swiss Army Knife to Cut Malaria Transmission
Inside Job: Viruses Transfer cGAMP between Cells
The Yeast Saccharomyces cerevisiae: A Versatile Model System for the Identification and Characterization of Bacterial Virulence Proteins  Keri A. Siggers,
Chapter 12-1 DNA Part 1.
Staphylococcus aureus Osteomyelitis: Bad to the Bone
Bacteria Moving into Focus of Human Cancer
For HIV, It's Never Too Late to Grow Up
Wilbert Bitter, Coen Kuijl  Cell Host & Microbe 
How Fungi Have Shaped Our Understanding of Mammalian Immunology
Dr. Israa ayoub alwan Lec – 1-))
Life-Saving Degeneracy in the Human Immune System
Experiments that led to the discovery of DNA
Dectin-1 Exerts Dual Control in the Gut
The Mammalian Gut as a Matchmaker
A Host MicroRNA Brokers Truce with HSV-1
Pneumococcus Adapts to the Sickle Cell Host
Don’t Bite the Hand that Feeds You
West African Ebola Virus Strains: Unstable and Ready to Invade?
Mother's Milk and Intrinsic Immunity
Presentation transcript:

CRISPR-Cas: To Take Up DNA or Not—That Is the Question Ariel D. Weinberger, Michael S. Gilmore  Cell Host & Microbe  Volume 12, Issue 2, Pages 125-126 (August 2012) DOI: 10.1016/j.chom.2012.07.007 Copyright © 2012 Elsevier Inc. Terms and Conditions

Figure 1 CRISPR Blocks Rough-to-Smooth Transformation In Vivo (Top row) The seminal 1928 experiments of Griffith (1928), who found that injection of a rough (unencapsulated) strain of S. pneumoniae rarely killed mice (top left), whereas injection of a smooth (encapsulated) strain did, and the smooth strain could be recovered from the dead mouse. Injection of heat-killed encapsulated bacteria (gray smooth) did not kill mice, but the combination of live rough S. pneumoniae together with heat-killed encapsulated S. pneumoniae established a productive infection that killed the mice. Moreover, when the bacteria recovered from the dead mice were cultured, they had “transformed” from rough to smooth (Griffith, 1928). In the present work (Bikard et al. (2012) showed that if the rough strain carried a functional CRISPR-Cas system that was designed to target a capsule gene, the transformation to smooth, virulent S. pneumoniae was blocked. Further, these investigators showed that when they forced the experiment using larger doses of bacteria, one mouse died and smooth bacteria were in fact recovered. These bacteria had mutated their CRISPR-Cas system, rendering it nonfunctional and unable to block the uptake of capsular DNA. Cell Host & Microbe 2012 12, 125-126DOI: (10.1016/j.chom.2012.07.007) Copyright © 2012 Elsevier Inc. Terms and Conditions