Sigma factor

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'''Sigma (σ) factor''' is the peoptide subunit needed for the initiation of RNA transcription in prokaryotic organisms <scene name='59/591940/Sigma_factor_in_enzyme/1'>as seen here</scene>. As opposed to eukaryotes, who utilize a variety of proteins to initiate gene transcription, prokaryotic transcription is initiated almost completely by a σ-factor. The large and biologically essential protein, RNA polymerase (RNAP), contains one σ-subunit, which binds <scene name='59/591940/Dna_promoter/3'>DNA promoter sequences</scene>, located upstream of transcription start sites.
'''Sigma (σ) factor''' is the peoptide subunit needed for the initiation of RNA transcription in prokaryotic organisms <scene name='59/591940/Sigma_factor_in_enzyme/1'>as seen here</scene>. As opposed to eukaryotes, who utilize a variety of proteins to initiate gene transcription, prokaryotic transcription is initiated almost completely by a σ-factor. The large and biologically essential protein, RNA polymerase (RNAP), contains one σ-subunit, which binds <scene name='59/591940/Dna_promoter/3'>DNA promoter sequences</scene>, located upstream of transcription start sites.
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== Specific Function and Structure ==
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== Function and Structure ==
The '''σ-factor''' performs two chief functions: to direct the catalytic core of RNAP to the promotoer upstream of the +1 start site of transcription, and finally to assist in the initiation of strand seperation of double-helical DNA, forming the transcription "bubble." Each gene promoter utilizes a specific promoter region about 40 bp upstream of the transcription start site, and therefore different σ-factors play a role in the regulation of different genes. This process, which includes association of the σ-factor with RNAP to recognize and open DNA at the promoter site, followed by dissociation of the σ to allow elongation, which can then activate additional RNAP enzymes, is referred to as the '''σ-cycle'''.
The '''σ-factor''' performs two chief functions: to direct the catalytic core of RNAP to the promotoer upstream of the +1 start site of transcription, and finally to assist in the initiation of strand seperation of double-helical DNA, forming the transcription "bubble." Each gene promoter utilizes a specific promoter region about 40 bp upstream of the transcription start site, and therefore different σ-factors play a role in the regulation of different genes. This process, which includes association of the σ-factor with RNAP to recognize and open DNA at the promoter site, followed by dissociation of the σ to allow elongation, which can then activate additional RNAP enzymes, is referred to as the '''σ-cycle'''.
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===Domains===
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===Domain Strucure & DNA interactions===
There are many types of σ-subunits, and each recognizes a unique promoter sequence. Furthmore, each unique σ is composed of a variable number of structured domains. The simplest σ-factors have two domains, few have three, and most, called '''housekeeping σ-factors''', have 4 domains, given the names σ(4), σ(3), σ(2), and σ(1.1). All domains are linked by very flexible peptide '''linkers''' which can extend very long distances. Each of these domains utilizes DNA-binding determinants, or domains that recognize specific sequences and conformations in DNA. Most commonly, these recognized sequences occur at the -35 and -10 locations upstream of the +1 site. One such DNA-binding motif, '''the helix-turn-helix motif''' (<scene name='59/591940/Hth_motif/2'>HTH</scene>), helps specifically recognize DNA promoters at both the -35 and -10 positions. This HTH motif, used by most σ-factors, maintains its specificity and accuracy by binding in the '''major groove''' of DNA, where it can interact with the base pairs in the DNA double-helix. In many prokaryotes, these portions of DNA maintain consensus adenosine and thymine sequences, such as <scene name='59/591940/Ta_sequence/1'>TATAAT</scene>.
There are many types of σ-subunits, and each recognizes a unique promoter sequence. Furthmore, each unique σ is composed of a variable number of structured domains. The simplest σ-factors have two domains, few have three, and most, called '''housekeeping σ-factors''', have 4 domains, given the names σ(4), σ(3), σ(2), and σ(1.1). All domains are linked by very flexible peptide '''linkers''' which can extend very long distances. Each of these domains utilizes DNA-binding determinants, or domains that recognize specific sequences and conformations in DNA. Most commonly, these recognized sequences occur at the -35 and -10 locations upstream of the +1 site. One such DNA-binding motif, '''the helix-turn-helix motif''' (<scene name='59/591940/Hth_motif/2'>HTH</scene>), helps specifically recognize DNA promoters at both the -35 and -10 positions. This HTH motif, used by most σ-factors, maintains its specificity and accuracy by binding in the '''major groove''' of DNA, where it can interact with the base pairs in the DNA double-helix. In many prokaryotes, these portions of DNA maintain consensus adenosine and thymine sequences, such as <scene name='59/591940/Ta_sequence/1'>TATAAT</scene>.
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===Transcription Bubble===
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The <scene name='59/591940/Transcription_bubble/1'>transcription bubble</scene>, also referred to as the '''open complex''' is formed through the common '''housekeeping σ factors''' which unwind about 13 bp of duplex DNA in an ATP independent process. Research has shown that σ factors require invariant basic and aromatic residues (Phe, Tyr, Trp) critical for this formation. The process of bubble formation begins at the -11 formation (usually A) and propogates to +1 site, through a phenomenon called <scene name='59/591940/Transcription_bubble_flipped/1'>Base Flipping</scene>, which interrupts the stacking interactions stabilizing the double helix conformation. As this process occurs and the DNA transitions into the open promoter complex, certain RNAP-σ contacts are lost, initiating the dissociation of σ. In summary, the processes of -35 and -10 motif sequence recognition and helix strand separation are coupled by the σ factor.
===Restriction===
===Restriction===
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An additional method of restriction is through the action of '''anti-σ's''', which act by making stable interactions with σ-domains, such as σ
An additional method of restriction is through the action of '''anti-σ's''', which act by making stable interactions with σ-domains, such as σ
(4), which allows them to make energy-favorable interactions with RNAP residues. This causes a cascading "peeling off" effect of other σ-domains from the RNAP, preventing any interaction with duplex DNA and inhibiting transcription in an analogous process to competitive inhibition.
(4), which allows them to make energy-favorable interactions with RNAP residues. This causes a cascading "peeling off" effect of other σ-domains from the RNAP, preventing any interaction with duplex DNA and inhibiting transcription in an analogous process to competitive inhibition.
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===Transcription Bubble===
 
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The <scene name='59/591940/Transcription_bubble/1'>transcription bubble</scene>, also referred to as the '''open complex''' is formed through the common '''housekeeping σ factors''' which unwind about 13 bp of duplex DNA in an ATP independent process. Research has shown that σ factors require invariant basic and aromatic residues (Phe, Tyr, Trp) critical for this formation. The process of bubble formation begins at the -11 formation (usually A) and propogates to +1 site, through a phenomenon called <scene name='59/591940/Transcription_bubble_flipped/1'>Base Flipping</scene>, which interrupts the stacking interactions stabilizing the double helix conformation. As this process occurs and the DNA transitions into the open promoter complex, certain RNAP-σ contacts are lost, initiating the dissociation of σ. In summary, the processes of -35 and -10 motif sequence recognition and helix strand separation are coupled by the σ factor.
 
== Gene Regulation and Differentiation ==
== Gene Regulation and Differentiation ==

Revision as of 02:55, 14 October 2014

Structure of sigma factor of E.Coli RNAP in complex with Promoter DNA (PDB code 4lup).

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Proteopedia Page Contributors and Editors (what is this?)

Wally Novak, Michal Harel

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