Spliceozymes: ribozymes that remove introns from pre-mRNAs in trans.
Group I introns are pre-mRNA introns that do not require the spliceosome for their removal. Instead, they fold into complex three-dimensional structures and catalyze two transesterification reactions, thereby excising themselves and joining the flanking exons. These catalytic RNAs (ribozymes) have b...
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doaj-4c1aafcf84af416b840e3feb2c07887c2020-11-24T22:08:10ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0197e10193210.1371/journal.pone.0101932Spliceozymes: ribozymes that remove introns from pre-mRNAs in trans.Zhaleh N AminiKaren E OlsonUlrich F MüllerGroup I introns are pre-mRNA introns that do not require the spliceosome for their removal. Instead, they fold into complex three-dimensional structures and catalyze two transesterification reactions, thereby excising themselves and joining the flanking exons. These catalytic RNAs (ribozymes) have been modified previously to work in trans, whereby the ribozymes can recognize a splice site on a substrate RNA and replace the 5'- or 3'-portion of the substrate. Here we describe a new variant of the group I intron ribozyme from Tetrahymena that recognizes two splice sites on a substrate RNA, removes the intron sequences between the splice sites, and joins the flanking exons, analogous to the action of the spliceosome. This 'group I spliceozyme' functions in vitro and in vivo, and it is able to mediate a growth phenotype in E. coli cells. The intron sequences of the target pre-mRNAs are constrained near the splice sites but can carry a wide range of sequences in their interior. Because the splice site recognition sequences can be adjusted to different splice sites, the spliceozyme may have the potential for wide applications as tool in research and therapy.http://europepmc.org/articles/PMC4094466?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Zhaleh N Amini Karen E Olson Ulrich F Müller |
spellingShingle |
Zhaleh N Amini Karen E Olson Ulrich F Müller Spliceozymes: ribozymes that remove introns from pre-mRNAs in trans. PLoS ONE |
author_facet |
Zhaleh N Amini Karen E Olson Ulrich F Müller |
author_sort |
Zhaleh N Amini |
title |
Spliceozymes: ribozymes that remove introns from pre-mRNAs in trans. |
title_short |
Spliceozymes: ribozymes that remove introns from pre-mRNAs in trans. |
title_full |
Spliceozymes: ribozymes that remove introns from pre-mRNAs in trans. |
title_fullStr |
Spliceozymes: ribozymes that remove introns from pre-mRNAs in trans. |
title_full_unstemmed |
Spliceozymes: ribozymes that remove introns from pre-mRNAs in trans. |
title_sort |
spliceozymes: ribozymes that remove introns from pre-mrnas in trans. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2014-01-01 |
description |
Group I introns are pre-mRNA introns that do not require the spliceosome for their removal. Instead, they fold into complex three-dimensional structures and catalyze two transesterification reactions, thereby excising themselves and joining the flanking exons. These catalytic RNAs (ribozymes) have been modified previously to work in trans, whereby the ribozymes can recognize a splice site on a substrate RNA and replace the 5'- or 3'-portion of the substrate. Here we describe a new variant of the group I intron ribozyme from Tetrahymena that recognizes two splice sites on a substrate RNA, removes the intron sequences between the splice sites, and joins the flanking exons, analogous to the action of the spliceosome. This 'group I spliceozyme' functions in vitro and in vivo, and it is able to mediate a growth phenotype in E. coli cells. The intron sequences of the target pre-mRNAs are constrained near the splice sites but can carry a wide range of sequences in their interior. Because the splice site recognition sequences can be adjusted to different splice sites, the spliceozyme may have the potential for wide applications as tool in research and therapy. |
url |
http://europepmc.org/articles/PMC4094466?pdf=render |
work_keys_str_mv |
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