Posttranscriptional Modification of RNA Overview

 
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A primary transcript 
A primary transcript 
is the initial, linear, RNA copy of a
transcription unit—the segment of DNA between specific
initiation and termination sequences.
The primary transcripts of both prokaryotic and eukaryotic
tRNA and rRNA are posttranscriptionally modified by
cleavage of the original transcripts by ribonucleases.
cleavage of the original transcripts by ribonucleases.
tRNAs are then further modified to help give each species
its unique identity.
In contrast, prokaryotic mRNA is generally identical to its
primary transcript, whereas eukaryotic mRNA is
extensively modified both co- and posttranscriptionally.
 
A. Ribosomal RNA
A. Ribosomal RNA
Posttranscriptional processing of eukaryotic
ribosomal RNA by 
ribonucleases (RNases).
 
o
rRNAs of both prokaryotic and
eukaryotic cells are generated from long
precursor molecules called pre-rRNAs.
o
The 23S, 16S, and 5S rRNA of
prokaryotes are produced from a single
pre-rRNA molecule, as are the 28S, 18S,
and 5.8S rRNA of eukaryotes.
o
The pre-rRNAs are cleaved by
ribonucleases to yield intermediate-
sized pieces of rRNA, which are further
processed (trimmed by exonucleases
and modified at some bases and
riboses) to produce the required RNA
species.
 
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A. Primary tRNA transcript. B. Functional tRNA after posttranscriptional
modification. Modified bases include D (dihydrouracil), ψ (pseudouracil),
and m, which means that the base has been methylated.
 
o
Both eukaryotic and prokaryotic tRNA are also made from
longer precursor molecules that must be modified.
o
Sequences at both ends of the molecule are removed and, if
present, an intron is removed from the anticodon loop by
nucleases.
 
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The collection of all the primary transcripts synthesized in the
nucleus by RNA polymerase II is known as heterogeneous nuclear
RNA (hnRNA).
The pre-mRNA components of hnRNA undergo extensive co- and
posttranscriptional modification in the nucleus.
These modifications usually include:
These modifications usually include:
 
1. 5’- Capping: 7-Methyl-guanosine
1. 5’- Capping: 7-Methyl-guanosine
2. 3’- Poly-A tail addition
2. 3’- Poly-A tail addition
3. Removal of introns
3. Removal of introns
4. Alternative splicing of mRNA molecules
4. Alternative splicing of mRNA molecules
 
1. 5’- Capping: 7-Methyl-guanosine
1. 5’- Capping: 7-Methyl-guanosine
 
o
The cap is a 7-methylguanosine attached “backward” to the 5'-terminal end of the mRNA,
forming an unusual 5'→5' triphosphate linkage.
o
Creation of the cap requires removal of the γ phosphate from the 5’-triphosphate of the
premRNA, followed by addition of GMP (from GTP) by the 
nuclear enzyme
nuclear enzyme
guanylyltransferase.
guanylyltransferase.
o
Methylation of this terminal guanine occurs in the 
cytosol
cytosol
, and is catalyzed by guanine-7-
methyltransferase. 
S-adenosylmethionine
S-adenosylmethionine
 is the source of the methyl group Additional
methylation steps may occur.
o
The addition of this 7-methylguanosine “cap” helps stabilize the mRNA, and permits
The addition of this 7-methylguanosine “cap” helps stabilize the mRNA, and permits
initiation of translation.
initiation of translation.
o
Eukaryotic mRNAs lacking the cap are not efficiently translated.
 
2. 3’- Poly-A tail addition
2. 3’- Poly-A tail addition
 
Most eukaryotic mRNA have a chain of 40–200 adenine nucleotides
attached to the 3'-end.
This poly-A tail is not transcribed from the DNA, but rather is added
after transcription by the nuclear enzyme, polyadenylate polymerase,
using ATP as the substrate.
The mRNA is cleaved downstream of a consensus sequence, called the
polyadenylation signal sequence (AAUAAA), found near the 3'-end of
the RNA, and the poly-A tail is added to the new 3'-end.
These tails help stabilize the mRNA, facilitate its exit from the nucleus,
and aid in translation. After the mRNA enters the cytosol, the poly-A tail
is gradually shortened.
 
3. Removal of introns
3. Removal of introns
 
Maturation of eukaryotic mRNA usually involves the removal of RNA
sequences (introns, or intervening sequences), which do not code for
protein from the primary transcript.
The remaining coding sequences, the exons, are joined together to form
the mature mRNA.
The process of removing introns and joining exons is called splicing.
The molecular complex that accomplishes these tasks is known as the
spliceosome. A few eukaryotic primary transcripts contain no introns,
for example,
those from histone genes.
Others contain a few introns, whereas some, such as the primary
transcripts for the α chains of collagen, contain more than 50
intervening sequences that must be removed before mature mRNA is
ready for translation.
Splicing. snRNP = small nuclear
Splicing. snRNP = small nuclear
ribonucleoprotein particle.
ribonucleoprotein particle.
 
4. Alternative splicing of mRNA molecules
4. Alternative splicing of mRNA molecules
 
The pre-mRNA molecules from
some genes can be spliced in
alternative ways in different
tissues.
This produces multiple variations
of the mRNA and, therefore, of its
protein product.
This appears to be a mechanism
for producing a diverse set of
proteins from a limited set of
genes.
Alternative splicing: A diverse set
of proteins from a small set of
genes
 
Posttranscriptionally modified by cleavage of the original transcripts by
ribonucleases.
rRNA of both prokaryotic and eukaryotic cells are synthesized from long
precursor molecules called preribosomal RNA.
These precursors are cleaved and trimmed by ribonucleases, producing the three
largest rRNA, and bases and sugars are modified.
Eukaryotic 5S rRNA is synthesized by RNA polymerase III , and is modified
separately.
Prokaryotic mRNA is generally identical to its primary transcript, whereas
eukaryotic mRNA is extensively modified co- and posttranscriptionally.
Most eukaryotic mRNAs also contain intervening sequences (introns) that must
be removed to make the mRNA functional.
Their removal, as well as the joining of expressed sequences (exons), requires a
spliceosome composed of small, nuclear ribonucleoprotein particles that mediate
the process of splicing.
Eukaryotic mRNA is monocistronic, containing information from just one gene.
Prokaryotic and eukaryotic tRNA are also made from longer precursor molecules.
 If present, an intron is removed by nucleases, and both ends of the molecule are
trimmed by ribonucleases. A 3'-CCA sequence is added, and bases at specific
positions are modified, producing “unusual” bases.
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A primary transcript is the initial RNA copy of a transcription unit, subject to posttranscriptional modifications like cleavage and further alterations to form functional tRNAs, rRNAs, and mRNAs. In eukaryotic cells, pre-rRNAs and pre-tRNAs undergo processing by ribonucleases to yield mature RNA species, while eukaryotic mRNA undergoes extensive co- and posttranscriptional modifications. The process involves the removal of introns, alternative splicing, capping with 7-Methyl-guanosine, and addition of poly-A tails. This comprehensive overview discusses the intricate mechanisms involved in RNA modifications across different RNA types.


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  1. Posttranscriptional Modification of RNA

  2. A primary transcript is the initial, linear, RNA copy of a transcription unit the segment of DNA between specific initiation and termination sequences. The primary transcripts of both prokaryotic and eukaryotic tRNA and rRNA are posttranscriptionally modified by cleavage of the original transcripts by ribonucleases. tRNAs are then further modified to help give each species its unique identity. In contrast, prokaryotic mRNA is generally identical to its primary transcript, whereas extensively modified both co- and posttranscriptionally. eukaryotic mRNA is

  3. A. Ribosomal RNA rRNAs eukaryotic cells are generated from long precursor molecules called pre-rRNAs. The 23S, 16S, and prokaryotes are produced from a single pre-rRNA molecule, as are the 28S, 18S, and 5.8S rRNA of eukaryotes. The pre-rRNAs ribonucleases to yield intermediate- sized pieces of rRNA, which are further processed (trimmed by exonucleases and modified at riboses) to produce the required RNA species. of both prokaryotic and o 5S rRNA of o are cleaved by o some bases and Posttranscriptional processing of eukaryotic ribosomal RNA by ribonucleases (RNases).

  4. B. Transfer RNA A. Primary tRNA transcript. B. Functional tRNA after posttranscriptional modification. Modified bases include D (dihydrouracil), (pseudouracil), and m, which means that the base has been methylated.

  5. Both eukaryotic and prokaryotic tRNA are also made from longer precursor molecules that must be modified. Sequences at both ends of the molecule are removed and, if present, an intron is removed from the anticodon loop by nucleases. o o

  6. C. Eukaryotic mRNA The collection of all the primary transcripts synthesized in the nucleus by RNA polymerase II is known as heterogeneous nuclear RNA (hnRNA). The pre-mRNA components of hnRNA undergo extensive co- and posttranscriptional modificationin the nucleus. These modifications usually include: 1. 5 - Capping: 7-Methyl-guanosine 2. 3 - Poly-A tail addition 3. Removal of introns 4. Alternative splicing of mRNA molecules

  7. 1. 5- Capping: 7-Methyl-guanosine oThe cap is a 7-methylguanosine attached backward to the 5'-terminal end of the mRNA, forming an unusual 5' 5'triphosphate linkage. oCreation of the cap requires removal of the phosphate from the 5 -triphosphate of the premRNA, followed by addition of GMP guanylyltransferase. oMethylation of this terminal guanine occurs in the cytosol, and is catalyzed by guanine-7- methyltransferase. S-adenosylmethionine is the source of the methyl group Additional methylation steps may occur. oThe addition of this 7-methylguanosine cap helps stabilize the mRNA, and permits initiation of translation. oEukaryotic mRNAs lacking the cap are not efficiently translated. (from GTP) by the nuclear enzyme

  8. 2. 3- Poly-A tail addition Most eukaryotic mRNA have a chain of 40 200 adenine nucleotides attached to the 3'-end. This poly-A tail is not transcribed from the DNA, but rather is added after transcription by the nuclear enzyme, polyadenylate polymerase, using ATP as the substrate. The mRNA is cleaved downstream of a consensus sequence, called the polyadenylation signal sequence (AAUAAA), found near the 3'-end of the RNA, and the poly-A tailis added to the new 3'-end. These tails help stabilize the mRNA, facilitate its exit from the nucleus, and aid in translation. After the mRNA enters the cytosol, the poly-A tail is gradually shortened.

  9. 3. Removal of introns Maturation of eukaryotic mRNA usually involves the removal of RNA sequences (introns, or intervening sequences), which do not code for proteinfromthe primary transcript. The remaining coding sequences, the exons, are joined together to form the maturemRNA. The process of removing introns and joining exons is called splicing. The molecular complex that accomplishes these tasks is known as the spliceosome. A few eukaryotic primary transcripts contain no introns, for example, those from histone genes. Others contain a few introns, whereas some, such as the primary transcripts for the chains of collagen, contain more than 50 intervening sequences that must be removed before mature mRNA is ready for translation.

  10. Splicing. snRNP = small nuclear ribonucleoprotein particle.

  11. 4. Alternative splicing of mRNA molecules The pre-mRNA molecules from some genes can be spliced in alternative ways tissues. This produces multiple variations of the mRNA and, therefore, of its protein product. This appears to be a mechanism for producing a diverse set of proteins from a limited set of genes. Alternative splicing: A diverse set of proteins from a small set of genes in different

  12. Posttranscriptionally modified by cleavage of the original transcripts by ribonucleases. rRNA of both prokaryotic and eukaryotic cells are synthesized from long precursor molecules called preribosomal RNA. These precursors are cleaved and trimmed by ribonucleases, producing the three largest rRNA, and bases and sugars are modified. Eukaryotic 5S rRNA is synthesized by RNA polymerase III , and is modified separately. Prokaryotic mRNA is generally identical to its primary transcript, whereas eukaryotic mRNA is extensively modified co- and posttranscriptionally. Most eukaryotic mRNAs also contain intervening sequences (introns) that must be removed to make the mRNA functional. Their removal, as well as the joining of expressed sequences (exons), requires a spliceosome composed of small, nuclear ribonucleoprotein particles that mediate the process of splicing. Eukaryotic mRNA is monocistronic, containing information from just one gene. Prokaryotic and eukaryotic tRNA are also made from longer precursor molecules. If present, an intron is removed by nucleases, and both ends of the molecule are trimmed by ribonucleases. A 3'-CCA sequence is added, and bases at specific positions are modified, producing unusual bases.

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