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Messenger RNA in Eukaryotes
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Abstract
The concept that eukaryotic gene expression is primarily regulated at the level of RNA (ribonucleic acid) polymerase II recruitment to a promoter has changed dramatically during the past decades. Changes such as mRNA capping, splicing, polyadenylation, editing as well as various chemical modifications produce a huge variety of unique mRNA species. The mRNA factory model suggests that transcription and mRNA processing are intimately coupled. Thus, the elongating RNA polymerase II, via its carboxy‐terminal domain (CTD), recruits key factors required for the proper capping, splicing and polyadenylation to the nascent transcript. Furthermore, factors controlling the speed of elongation, such as nucleosome occupancy and modification, also partake in the generation of alternatively spliced mRNA, a process that represents an important regulatory level at which eukaryotes can expand the coding capacity of their genomes.
Key Concepts
mRNA processing events, such as capping, splicing and polyadenylation, are coordinated and occur predominantly co‐transcriptionally.
Different phosphorylation patterns of the carboxy‐terminal domain (CTD) control the temporal recruitment of capping, splicing and polyadenylation factors to the elongating RNA polymerase II.
Nucleosomes are preferentially found at exonic sequences and influence the speed of elongation and outcome of co‐transcriptional splicing.
Essentially, all eukaryotic genes produce alternatively spliced and polyadenylated mRNAs.
Alternative splicing greatly expands the coding capacity of a gene; that is one gene does not only code for one protein.
mRNA splicing, mRNA export and nonsense‐mediated mRNA decay are tightly coupled reactions that ensure that erroneous mRNAs are destroyed.
RNA editing is an important regulatory mechanism to produce protein diversity and control various aspects of the mRNA life cycle.
Dynamic ribonucleotide modifications, such as adenosine methylation, present a novel way to regulate mRNA stability, localisation and translation.
Title: Messenger
RNA
in Eukaryotes
Description:
Abstract
The concept that eukaryotic gene expression is primarily regulated at the level of RNA (ribonucleic acid) polymerase II recruitment to a promoter has changed dramatically during the past decades.
Changes such as mRNA capping, splicing, polyadenylation, editing as well as various chemical modifications produce a huge variety of unique mRNA species.
The mRNA factory model suggests that transcription and mRNA processing are intimately coupled.
Thus, the elongating RNA polymerase II, via its carboxy‐terminal domain (CTD), recruits key factors required for the proper capping, splicing and polyadenylation to the nascent transcript.
Furthermore, factors controlling the speed of elongation, such as nucleosome occupancy and modification, also partake in the generation of alternatively spliced mRNA, a process that represents an important regulatory level at which eukaryotes can expand the coding capacity of their genomes.
Key Concepts
mRNA processing events, such as capping, splicing and polyadenylation, are coordinated and occur predominantly co‐transcriptionally.
Different phosphorylation patterns of the carboxy‐terminal domain (CTD) control the temporal recruitment of capping, splicing and polyadenylation factors to the elongating RNA polymerase II.
Nucleosomes are preferentially found at exonic sequences and influence the speed of elongation and outcome of co‐transcriptional splicing.
Essentially, all eukaryotic genes produce alternatively spliced and polyadenylated mRNAs.
Alternative splicing greatly expands the coding capacity of a gene; that is one gene does not only code for one protein.
mRNA splicing, mRNA export and nonsense‐mediated mRNA decay are tightly coupled reactions that ensure that erroneous mRNAs are destroyed.
RNA editing is an important regulatory mechanism to produce protein diversity and control various aspects of the mRNA life cycle.
Dynamic ribonucleotide modifications, such as adenosine methylation, present a novel way to regulate mRNA stability, localisation and translation.
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