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What are Introns and Exons?


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Introns and exons are nucleotide sequences within a gene. Introns are removed by RNA splicing as RNA matures, meaning that they
are not expressed in the nal messenger RNA (mRNA) product, while exons go on to be covalently bonded to one another in order
to create mature mRNA.

Introns can be considered as intervening sequences, and exons as expressed sequences.

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What are Exons?


Exons are nucleotide sequences in DNA and RNA that are conserved in the creation of mature RNA. The process by which DNA is
used as a template to create mRNA is called transcription.

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Exons usually include both the 5’- and 3’- untranslated regions of mRNA, which contain start and stop codons, in addition to any
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What are Introns?
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Introns are nucleotide sequences in DNA and RNA that do not directly code for proteins, and are removed during the precursor
messenger RNA (pre-mRNA) stage of maturation of mRNA byLife
RNA splicing.
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Introns can range in size from 10’s of base pairs to 1000’s White
of base pairs,(/life-sciences/whitepapers)
Papers and can be found in a wide variety of genes that generate
RNA in most living organisms, including viruses.
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Four distinct types of introns have been identi ed:
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Introns in protein coding genes, removed by spliceosomes


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Introns in tRNA genes, which are removed by proteins
Self-splicing introns, which catalyse their own removal from mRNA, tRNA, and rRNA precursors Webinars
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triphosphate (GTP), or another nucleotide cofactor (Group 1)
Self-splicing introns, which do not require GTP in order to remove themselves
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It is vital for the introns to be removed precisely, as any left-over intron nucleotides, or deletion of exon nucleotides, may result in a
faulty protein being produced. This is because the amino acids that make up proteins are joined together based on codons, which
consist of three nucleotides. An imprecise intron removal thus may result in a frameshift, which means that the genetic code would
be read incorrectly.

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Introns vs Exons
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RNA Splicing
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RNA splicing is the method by which pre-mRNA is made into mature mRNA, by removal of
introns and joining together of exons. Several methods of splicing exist, depending on the Related Stories
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organism, type of RNA or intron structure, and the presence of catalysts.
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Introns possess a highly conserved GU sequence at their 5’ end, known as the donor site, New drug provides hope for
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and a highly conservedMEDICAL HOME (/MEDICAL)
AG sequence at the 3’ end, called the acceptor site. A large RNA- patients with Duchenne
protein complex, the spliceosome, made up of ve small nuclear ribonucleoproteins muscular dystrophy
(snRNPs) recognise the start and end points of the intron thanksAbout (/life-sciences/about)
to these sites, and (/news/20190710/New-drug-
catalyse
(/)the removal of the intron accordingly. The spliceosome forms the intron into a provides-hope-for-patients-
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sequences also exist, known as minor spliceosomes. Scientists uncover functions of
White Papers (/life-sciences/whitepapers) mysterious organelles in stress
tRNA splicing is far rarer, though does occur in all three major domains of life, bacteria, response
archaea and eukarya. Multiple enzymes ll the role of snRNPs in a step-wise
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biochemical reactions, ribozymes. Group 1 introns are attacked at the 5’ splice site by a
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leading to the 3’OH of the adjacent exon to become nucleophilic and thus bond to the 5’
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spliced in a similar way, though with the use of a speci c adenosine that attacks the 5’
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Alternative Splicing
Alternative splicing refers to the way that di erent combinations of exons can be joined together, resulting in a single gene coding
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for multiple proteins. Walter Gilbert rst put this idea forward, and he proposed that the di erent permutations of exons could
produce di erent protein isoforms. These in turn would have di erent chemical and biological activities.
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It is now thought that between 30 and 60% of human genes undergo alternative splicing. Moreover, over 60% of disease-causing
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mutations in humans are related to splice errors, rather than mistakes in coding sequences.

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One example of a human gene that undergoes alternative splicing is (/life-sciences/about)
bronectin, a glycoprotein that extends from the cell into the
extracellular
(/) matrix. Over 20 di erent isoforms of bronectin have been discovered. These have all been produced from di erent
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combinations of bronectin gene exons.

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scidiv.bellevuecollege.edu/rkr/Biology211/labs/pdfs/BetaGlobin211.pdf
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(http://scidiv.bellevuecollege.edu/rkr/Biology211/labs/pdfs/BetaGlobin211.pdf)
https://www.ncbi.nlm.nih.gov/books/NBK21475/ (https://www.ncbi.nlm.nih.gov/books/NBK21475)
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dwb4.unl.edu/.../Post-trans.html
(http://dwb4.unl.edu/Chem/CHEM869N/CHEM869NLinks/bssv01.lancs.ac.uk/ADS/BIOL253notes/Post-trans.html)
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sta www.fullcoll.edu/.../Solutions_Manual_Chapter_14.pdf
(http://sta www.fullcoll.edu/cyoung/notes/BIOL276%20Presentations/Solutions%20Manual/Solutions_Manual_Chapter_14.pdf)
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http://www.ncbi.nlm.nih.gov/pubmed/15217358 (http://www.ncbi.nlm.nih.gov/pubmed/15217358)
www.dartmouth.edu/~cbbc/courses/bio4/bio4-lectures/EukGenes.html (http://www.dartmouth.edu/~cbbc/courses/bio4/bio4-
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lectures/EukGenes.html)
www.nature.com/.../translation-dna-to-mrna-to-protein-393 (http://www.nature.com/scitable/topicpage/translation-dna-to-
mrna-to-protein-393)
www.nature.com/.../rna-splicing-introns-exons-and-spliceosome-12375 (http://www.nature.com/scitable/topicpage/rna-
splicing-introns-exons-and-spliceosome-12375)
www.psychiatry.wustl.edu/.../Modrek.pdf
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(http://www.psychiatry.wustl.edu/Resources/LiteratureList/2002/January/Modrek.pdf)
www.mimg.ucla.edu/.../%2829%29annurev.biochem.72.121801.161720.pdf
(http://www.mimg.ucla.edu/faculty/black/%2829%29annurev.biochem.72.121801.161720.pdf)  Accept
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highered.mcgraw-hill.com/.../bio30.swf::How%20Spliceosomes%20Process%20RNA (http://highered.mcgraw-
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Written by

Michael Greenwood (https://www.news-medical.net/life-sciences/authors/michael-greenwood)


Michael graduated from Manchester Metropolitan University with a B.Sc. in Chemistry in 2014, where he majored in organic, inorganic,
physical and analytical chemistry. He is currently completing a Ph.D. on the design and production of gold nanoparticles able to act as
multimodal anticancer agents, being both drug delivery platforms and radiation dose enhancers.

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Please explain why the paper "Lessons learned from next-generation (/opinion/1bf5453f-3977-43a6-88ba-652fbcc351d6.aspx)
B Chin says:
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June 29, 2013 at 12:27 AM (/opinion/1bf5453f-3977-43a6-88ba-652fbcc351d6.aspx)
Please explain why the paper "Lessons learned from next-generation sequencing in head and neck cancer" by Loyo et al in Head & Neck 35,
454 (march 2013) states Lab Equipment (/Life-Science-and-Laboratory)

"Tumor protein [gene] p53 is made of 11 exons, of which the rst is Interviews
noncoding...".
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It appears to me that Exons are any part of the DNA which encode for RNA, WHETHER OR NOT that RNA is an mRNA, one that eventually yields a
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protein.

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good information thank you . i want to know the role of natural selection (/opinion/5ca8308a-300b-4f5b-94 -3d26c979afd4.aspx)
Kekendo OD says:
March 30, 2017 at 6:56 PM (/opinion/5ca8308a-300b-4f5b-94 -3d26c979afd4.aspx)
good information thank you . i want to know the role of natural selection on exons and introns

Reply 0 0

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