Dear Steemit Friends,
In my previous article, I talked a bit on CRISPR and I have looked for good articles here on steemit that might explain the Biology of CRISPR. It was far and not complete, I am sure there are better articles outside the ecosystem. But in an effort to bring good content here, I took up the opportunity to make a short post on CRISPR which is Part 1 of 3 part series.
Before its mainstream adaptation into a genome editing technology in eukaryotes. CRISPR, an acronym for Clustered Regularly Interspaced Short Palindromic Repeats; was discovered in the genomes of bacteria and archea by the team led by Phlippe Horvath. It was described for the first time in a paper published in the journal Science on 23 March 2007. The paper titled "CRISPR Provides Acquired Resistance Against Viruses in Prokaryotes"; As a mechanism of resistance against bacteriophages.
Bacteriophages are abundant viruses that primarily "infect" bacteria. They are ubiquitous and abundant in nature and are very important in ecological and evolutionary aspects. Since they attack bacteria; as a countermeasure, bacteria have developed their own defense mechanisms. CRISPR is one such countermeasure that was described in the article.
The team used abacteriumm commonly used in industries; Streptococcus thermophilus as the model species. They compared closely related strains and identified that there were sites that varied a lot between species. Since the industrial species lack the resistance to bacteriophages and their wild cousins are resistant to the phage infection; They analysed these stretches of repeated sequences.
"CRISPR loci typically consist of several noncontiguous direct repeats separated by stretches of variable sequences called spacers and are oftentimes adjacent to cas genes (CRISPR-associated)"
Upon analysis, the phage resistant types had additional spacers in the CRISPR loci. To test their hypothesis that this was a sort of immune system; They challenged a strain found in the industry with different phages.
The authors then made classical studies of deleting the obtained spacers and introducing spacers to test the sensitivity against the resistance.
Image: By CtSkennerton (Own work), via Wikimedia Commons. Background by NIH
The stages of CRISPR immunity for each of the three major divisions.
(1) Acquisition begins by recognition of invading DNA by Cas1 and Cas2 and cleavage of a protospacer.
(2) The protospacer is ligated to the direct repeat adjacent to the leader sequence and
(3) single strand extension repairs the CRISPR and duplicates the direct repeat. The crRNA processing and interference stages occur differently in each of the three major CRISPR systems.
(4) The primary CRISPR transcript is cleaved by cas genes to produce crRNAs.
(5) In type I systems Cas6e/Cas6f cleave at the junction of ssRNA and dsRNA formed by hairpin loops in the direct repeat. Type II systems use a trans-activating (tracr) RNA to form dsRNA, which is cleaved by Cas9 and RNaseIII. Type III systems use a Cas6 homolog that does not require hairpin loops in the direct repeat for cleavage.
(6) In type II and type III systems secondary trimming is performed at either the 5’ or 3’ end to produce mature crRNAs.
(7) Mature crRNAs associate with Cas proteins to form interference complexes.
(8) In type I and type II systems, basepairing between the crRNA and the PAM causes degradation of invading DNA. Type III systems do not require a PAM for successful degradation and in type III-A systems basepairing occurs between the crRNA and mRNA rather than the DNA, targeted by type III-B systems.
The original paper can be accessed on Science Magazine.
Image Sources: All the images used are attributed to the corresponding authors. They are not mine. Please take time to check their galleries as it gives them more exposure and you will get to know their work better.
