BioQuakes

AP Biology class blog for discussing current research in Biology

Tag: RNA (Page 2 of 2)

CRISPR-Cas9 Can Now Be Applied to Not Only DNA But RNA

Anyone who has seen the movie Gattaca knows that the plot is set in a futuristic society that is able to edit the human genome. Of course, there’s a reason that it’s set in the future. Scientists of today couldn’t possibly dream of being able to edit genes in our DNA…right?

Well, wrong. Say hello to CRISPR-Cas9. CRISPER-Cas9 is, in short, a highly effective and popular DNA-editing technique that scientists started to use to sequence and edit human genes.

However, thanks to scientists at University of California-San Diego, CRISPR-Cas9 is not only limited to editing DNA. By altering only a few key features, this mechanism can now also be used with RNA, another highly important and fundamental molecule in the human body. CRISPR-Cas9 as of now can be used to track RNA in its movement, such as its many essential roles in protein synthesis. Below is a picture that briefly shows the importance of mRNA and tRNA:

 

Screen Shot 2016-04-11 at 12.01.31 AM

(Source: http://www.proteinsynthesis.org/protein-synthesis-steps/)

It’s an exciting development in that certain diseases, such as cancer and autism, are linked to mutations in RNA. By using CRISPR-Cas9 to their advantage, scientists could study the movement of RNA in the cell—and how and when it gets there—to track any defective RNA that can potentially lead to such diseases and then hopefully develop treatments. Gene Yeo, PhD, an associate professor of cellular and molecular medicine at UC-San Diego, expresses hope that “future developments could enable researchers to measure other RNA features or advance therapeutic approaches to correct disease-causing RNA behaviors”.

Intrigued? Confused? Please leave any comments or questions below!

 

Original Article

Forget DNA, Let’s Talk RNA!

8737208097_f9441a4000_b

Photo of RNA (licensing information here)

The genetic code within DNA is responsible for determining who we are and what we are capable of. Because of this, scientists have been interested in cracking the genetic code and finding ways to alter it. There are many diseases linked to DNA, as well as RNA. However, scientists have not been as successful in targeting RNA in living cells as they have been in targeting DNA. Recently, using CRISPR-Cas9, researchers at University of California, San Diego School of Medicine have figured out how to do what has been troubling scientists.

Senior author Dr. Gene Yeo described how the researchers at UCSD have been tracking the movement of RNA throughout cells and plan to measure other RNA features and help to correct disease-causing RNA behaviors using CRISPR-Cas9. The location of RNA in a cell determines whether proteins are produced at the right time and in the right place. When defective RNA transport occurs, diseases ranging from autism to cancer can occur. In order to successfully treat these conditions, researchers must find a way to track and measure the movement of RNA. This process was first seen with DNA: scientists found they could use CRISPR-Cas9 to track and edit genes in mammalian systems. Now, however, Yeo and his colleagues at UC Berkeley have started to target RNA in live cells (RNA-targeted Cas9 or RCas9), as well as DNA in live cells.

When CRISPR-Cas9 is used for normal DNA-involved purposes, researchers design “guide” RNA to match the DNA sequence of the gene Cas9 is targeting. The “guide” RNA then directs the Cas9 enzyme to the target spot in the genome. The Cas9 enzyme then cuts the DNA, which causes the DNA to break in a manner that inactivates the gene. Researchers can also replace the section of the genome next to the cut DNA with a corrected version of the gene. In order to allow Cas9 to work for RNA as well as DNA, work originated by co-author Dr. Jennifer Doudna at UC Berkeley laid a base foundation for researchers to design the PAMmer: a short nucleic acid. The PAMmer works with the “guide” RNA to direct Cas9 to an RNA molecule, instead of DNA.

All in all, CRISPR-Cas9 is responsible for a revolution in genomics with it’s ability to target and modify human DNA. Although this breakthrough is crucial, scientists are now trying to use their lead to target and modify RNA. With an extension on already existing research, there is no doubt that scientists will soon be able to do more than just track RNA. So, let’s forget about DNA and shine a light on RNA for a little while!

Source

Viruses are Like Felons, They Both Get Mugshots

Scientists at the Stanford University School of Medicine and three other schools have just discovered that a bacteria named Marinomonas mediterranea takes “RNA mug shots” to help recognize and defeat harmful viruses. The bacteria can take “RNA mugshots” or “DNA mugshots” depending on whether the invader is RNA-based or DNA-based.

Researchers want to use this technic to genetically form crops that have this virus-identifying property. Another use is to prevent viruses from infecting dairy products.

CRISPR is a new way of editing genomes that relates to this discovery. Bacteria takes pieces of DNA from cells and store them, also like “mugshots”.

RNA help DNA is coding, decoding, and expressing genes. By just getting a snapshot of a virus’ RNA or DNA, bacteria can identify this virus and destroy it in the future.

This finding is very new and so scientists are still studying how it exactly works and what its applications are. How do our readers think about it? Is this a surprising discovering or does it seem obvious? Were you aware that viruses have their own DNA and RNA? How do you think bacteria can apply this technic to other problems in the body, such as the regulation of cell production? Comment below on your scientific observations of this finding!

 

https://pixabay.com/en/virus-microbiology-cell-infection-163471/

Other sources:

https://www.sciencedaily.com/releases/2016/02/160225153423.htm 

http://kalen2utech.com/bacteria-take-rna-mug-shots-of-threatening-viruses/ 

http://www.technewscoverage.com/news/bacteria-take-rna-mug-shots-of-threatening-viruses.html 

 

Protein Structure May Lead to Cure for Ebola

For those who haven’t been keeping up with the latest in viral outbreaks, Ebola has been spreading throughout West Africa and has already taken the lives of 2,600 people since the outbreak in March 2014.  According to the World Health Organization , there are currently no certified vaccines or treatments for Ebola but a new breakthrough may have answers to developing a cure or vaccine for the deadly disease

Scientists at the University of Virginia have gotten their hands on a crystalized structure of the Ebola Nucleoprotein C-Terminal domain, which is an important protein used in replicating the virus.  The tertiary fold of the C-terminal is “unique in the RNA virus world,” claims structural biologist Dr. Zygmunt Derewenda, and this unique fold could ultimately lead to the foundation of drugs to prevent further infections.

The team was able to produce the protein by using E Coli as the protein factory.  So far, the protein demonstrates traits that are extremely unique and unlike other known proteins.  Evidence thus far has shown that the viral nucleoapsid is self assembled by the domain.  Insights and new research that the UVA team is conducting is paving the way to an Ebola anti-viral drug.

 

Ebola Virus Particles

 

Breakthrough in Epigenetics!

 

This file (Arabidopsis thaliana flower) is in public domain, not copyrighted, no rights reserved, free for any use

 

For several dozen years scientists have searched for a way to understand the role of a single RNA strand in gene expression.  Scientists have been without a method to pinpoint 1 type of RNA strand and isolate its effect thus discovering its influence and its corresponding proteins role in influencing the way our bodies work.

However a breakthrough was made this march regarding such obstacles.  A team of scientists from Michigan Technological University discovered a way to turn off small RNA strands in order to figure out what they are up to.  They did this by inserting their own custom DNA strand that codes for something called a small tandem target mimic or “STTM” into a plant known as “Arabidopsis“.  Inside the plant, these DNA strands gave rise to STTM’s that blocked the ability of a target RNA to express itself.  The particular target for the STTM was a type of RNA strand suspected to be involved with facilitating vertical growth of the plant.  The STTM’s stopped the RNA from being able to cut itself into smaller bits, and prompted the target RNA’s to destroy all of its own smaller RNA’s that would normally slice the target RNA.  This effectively lead to the disappearance of the target RNA’s protein products thus resulting in no expression of the gene the target RNA from transcribed from.

The result was outstanding.  “The control Arabidopsis plants grew upward on a central stem with regularly shaped leaves and stems. The mutant plants were smaller, tangled, and amorphous.”

The above process is said to be “a highly effective and versatile tool” for studying the functions of small RNA.  One researcher on the team who discovered this method stated that she intends to use this discovery to study type 2 diabetes.

 

Reference

http://www.sciencedaily.com/releases/2012/03/120301143756.htm

Tricky Viruses

Photo Credit: Foto_di_Signorina Flickr

           Strong viruses, such as HIV, make the body work for them. Researchers in Copenhagen have been studying how these viruses manage to take over the body. The virus takes over one cell and then uses the RNA to influence the DNA, giving the virus complete control over the cell. The RNA of the virus is similar to the RNA of the cell. Therefore, the ribosomes of the cell copy the sequence from the virus instead of the actual RNA. This causes the cell to produce the virus’ proteins.

                The RNA of the virus has what is called a pseudoknot. Pseudoknots are places on the RNA that the ribosomes must decipher before it can move on. The pseudoknot holds the sequence for key destructive proteins of the virus and once the ribosome deciphers it, those proteins are produced. This is how HIV can spread so rapidly in the body and can take such a hold over the host; it doesn’t do any of the work.

Can We Begin with a Moment of Silence?

In today’s world, there are more and more breaks in cancer research, and Dr. Sven Diederichs and his team are one more to add to the list.  Dr. Sven believes that “In many cancers we find that specific non- coding genes are particularly active. Therefore, we want to understand what the RNA molecules transcribed from these genes bring about in the tumor cells.”  Could this be the big answer? After all this time, could it be that it has been RNA molecules sending messages that create cancer.

Dr. Sven and his team came to this hypothesis and therefore created a method to find out the truth called “loss-of-function.”  In this experiment, scientists can silence a gene of a living cell and try to find changes in the cell’s behavior, metabolism, or physiology. They created this method on the use of zinc finger nucleases.

Once the scientist figured out how to make this method work, they were able to, for the first time, completely silence genes. Why is this important to cancer research? Dr. Sven believes that certain genes play a huge role in the development of cancer and are very active in tumor cells. If we have the chance to “shut down” these genes in RNA before they become active, we can ultimately prevent cancer.

In AP Biology class, we are learning about RNA transferring different kinds of information that stimulate cells to perform certain functions based on need, location and ability.  Are all these stimuli good? Or are they sending messages to create tumor cells?

We all know someone that has cancer, whether it’s your brother’s girlfriend’s uncle’s high school girlfriend, a friend of a friend, your best friend or it’s you. Everyone has a reason they want to get rid of such a terrible disease. So would you invest in this research or do you think its impossible to figure out which exact gene is the cause for all cancers?

Page 2 of 2

Powered by WordPress & Theme by Anders Norén

Skip to toolbar