RNA Transcription by RNA Polymerase: Prokaryotes vs Eukaryotes
By: Suzanne Clancy, Ph.D. © 2008 Nature Education
Citation: Clancy, S. (2008) RNA transcription by RNA polymerase: prokaryotes vs eukaryotes. Nature Education 1(1)
Gene
expression is linked to RNA transcription, which cannot happen without
RNA polymerase. However, this is where the similarities between
prokaryote and eukaryote expression end.
Every nucleated, diploid cell in the body contains the same DNA, or genome, yet
different cells appear committed to different specialized tasks—for example,
kidney cells absorb sodium, while pancreatic cells produce insulin. How
is this possible? The answer lies in differential use of the genome; in other
words, different cells within the body express different portions of their DNA.
This process, which begins with the transcription of DNA into RNA, ultimately leads
to changes in cell function. Changes in transcription are thus a fundamental
means by which cell function is regulated across species. In fact, even
single-celled organisms, such as bacteria, regulate gene transcription
depending on cues in their environments. Therefore, understanding how
transcription is regulated is fundamental to deciphering the mysteries of the
genome.
Central to the process of transcription is the complex of proteins known as the RNA polymerases. RNA polymerases have been found in all species, but the number and composition of these proteins vary across taxa. For instance, bacteria contain a single type of RNA polymerase, while eukaryotes (multicellular organisms and yeasts) contain three distinct types. In spite of these differences, there are striking similarities among transcriptional mechanisms. For example, all species require a mechanism by which transcription can be regulated in order to achieve spatial and temporal changes in gene expression. In order to fully understand what this means, it is first necessary to examine the mechanisms of RNA transcription in more detail.
Central to the process of transcription is the complex of proteins known as the RNA polymerases. RNA polymerases have been found in all species, but the number and composition of these proteins vary across taxa. For instance, bacteria contain a single type of RNA polymerase, while eukaryotes (multicellular organisms and yeasts) contain three distinct types. In spite of these differences, there are striking similarities among transcriptional mechanisms. For example, all species require a mechanism by which transcription can be regulated in order to achieve spatial and temporal changes in gene expression. In order to fully understand what this means, it is first necessary to examine the mechanisms of RNA transcription in more detail.
Transcription: An Overview
In all species, transcription begins with the binding of the RNA polymerase complex (or holoenzyme) to a special DNA sequence at the beginning of the gene known as the promoter.
Activation of the RNA polymerase complex enables transcription
initiation, and this is followed by elongation of the transcript. In
turn, transcript elongation leads to clearing of the promoter, and the
transcription process can begin yet again. Transcription can thus be
regulated at two levels: the promoter level (cis regulation) and the polymerase level (trans regulation). These elements differ among bacteria and eukaryotes.
Transcription in Bacteria
In bacteria, all transcription is performed by a single type
of RNA polymerase. This polymerase contains four catalytic subunits and a
single regulatory subunit known as sigma (s).
Interestingly, several distinct sigma factors have been identified, and each of
these oversees transcription of a unique set of genes. Sigma factors are thus
discriminatory, as each binds a distinct set of promoter sequences.
A striking example of the specialization of sigma factors for different gene promoters is provided by bacterial sporulation in the species Bacillus subtilis. This bacterium exists in two states: vegetative (growing) and sporulating. Genes involved in spore formation are not normally expressed during vegetative growth. Remarkably, expression of a gene encoding a novel sigma factor turns on the first genes for sporulation. Subsequent expression of different sigma factors then turns on new sets of genes needed later in the sporulation process (Losick & Stragier, 1992). Each of these sigma factors recognizes the promoters of the genes in its group, not those "seen" by other sigma factors. This simple example illustrates how transcription can be regulated in both cis and trans to cause changes in cell function. Therefore, while bacteria accomplish transcription of all genes using a single kind of RNA polymerase, the use of different sigma factor subunits provides an extra level of control.
A striking example of the specialization of sigma factors for different gene promoters is provided by bacterial sporulation in the species Bacillus subtilis. This bacterium exists in two states: vegetative (growing) and sporulating. Genes involved in spore formation are not normally expressed during vegetative growth. Remarkably, expression of a gene encoding a novel sigma factor turns on the first genes for sporulation. Subsequent expression of different sigma factors then turns on new sets of genes needed later in the sporulation process (Losick & Stragier, 1992). Each of these sigma factors recognizes the promoters of the genes in its group, not those "seen" by other sigma factors. This simple example illustrates how transcription can be regulated in both cis and trans to cause changes in cell function. Therefore, while bacteria accomplish transcription of all genes using a single kind of RNA polymerase, the use of different sigma factor subunits provides an extra level of control.
Transcription in Eukaryotes
"Christmas tree-like" structures can be visualized during active transcription.
Yeast
strains conditionally expressing either the U3 snoRNA or Utp7 from a
galactose promoter were used to make the chromatin spreads.
Eukaryotic
cells are more complex than bacteria in many ways, including in terms
of transcription. Specifically, in eukaryotes, transcription is achieved
by three different types of RNA polymerase
(RNA pol I-III). These polymerases differ in the number and type of
subunits they contain, as well as the class of RNAs they transcribe;
that is, RNA pol I transcribes ribosomal RNAs (rRNAs), RNA pol II
transcribes RNAs that will become messenger RNAs (mRNAs) and also small
regulatory RNAs, and RNA pol III transcribes small RNAs such as transfer
RNAs (tRNAs).
Because RNA pol II transcribes protein-encoding genes, it has
been of particular importance to scientists who study the regulation of
eukaryotic gene expression, and its function is well understood. For
example, researchers know that RNA pol II can bind to a DNA sequence
within the promoter of many genes, known as the TATA box,
to initiate transcription. Together with other common motifs (short
recognition sequences in the DNA), these elements constitute the core promoter.
However, changes in RNA pol II affinity and, therefore, gene expression
can be influenced by surrounding DNA sequences (enhancers), which in
turn recruit transcription factors. While these properties of
transcription regulation are very important, they remain an area of
active research.
Interestingly, RNA pol II is uniquely sensitive to amatoxins, such as a-amanitin of the extremely toxic Amanita
genus of mushrooms (Weiland, 1968), a fact that researchers have been
able to exploit for the purposes of polymerase studies - although
recreational mushroom hunters should beware! Thus, while eukaryotic
transcription is far more complex than bacterial transcription, the main
difference between the two types of transcription lies in RNA
polymerase.
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