Trans-Acting Factors Control Gene Expression
In general, why is any specific module in a promoter important. Two possible reasons can
be given: 1) The module is conserved in several promoters. Or 2) The module is shown to be a
binding site for a transcription factor. Thus any discussion of a
promoter and its relevant
sequences must consider these sequences and any proteins that may bind to them. Therefore the
transcription initiation complex is composed of promoter sequences and DNA binding proteins.
These two components of transcription are normally described as cis-acting elements and
trans-acting factors.
Cis-acting elements - DNA sequences in the vicinity of the structural portion of a gene that are
required for gene expression
As we have mentioned several genes seem to be transcribed coordinately. For example, the
different members of a storage protein or photosynthetic protein family are expressed at the same
time in development. These genes have sequence modules in common that control the coordinate
regulation. These modules are called response elements. These elements are a class of cis-acting
elements.
Features of Response Elements
- contain short consensus sequences
- modules are related but not identical
- not fixed in location but usually within 200 bp upstream of the transcription start site
- a single element is usually sufficient to confer a regulatory response
- can be located in a promoter or an enhancer
- assumed that a specific protein binds to the element and the presence of that protein is
developmentally regulated
Trans-acting factors - factors, usually considered to be proteins, that bind to the cis-acting
sequences to control gene expression
We have not discussed trans-acting factors yet. What are some of the properties of different
trans-acting factors:
- subunits of RNA polymerase
- bind to RNA Polymerase to stabilize the initiation complex
- bind to all promoters at specific sequences but not to RNA Polymerase (TFIID factor which
binds to the TATA box)
- bind to a few promoters and are required for transcription initiation; these are positive
regulators of gene expression
Those factors which bind to consensus module sequences can bind to any promoter that
contains the sequence. The binding of multiple factors, for example, multiple trans-acting factors
each with one of the four properties mentioned above, may be essential for transcription initiation.
Enhancers, which normally have a consensus 72 bp repeat sequence, have sites for multiple trans-
acting factors to bind. Thus genes with enhancers may require several complexes to be
constructed for gene expression to be initiated.
Functions Of Transcription Factors
- recognize target sequences in DNA
- interact with other transcription factors
These trans-acting factors can control gene expression in several ways:
- factor may be expressed in a specific tissue manner (spatial regulation)
- factor may be expressed in at specific time in development (temporal regulation)
- factor may require modification (phosphorylation)
- factor may be activated by ligand binding
- factor may be sequestered until an appropriate environmental signal allows it to interact with
the nuclear DNA
Each transcription factor has a characteristic motif. These motifs are short structures which
comprise only a small portion of the protein. These motifs are used to define a specific class of trans-acting
factors. The following are specific examples of trans-acting factors, each with a defined and
specific motif.
- steroid receptors
- zinc finger proteins - Zn++ binds at a specific site
- leucine zipper proteins - leucine appears every seven amino acids in a region of the protein
We now need to see how experiments are performed which determine that a trans-acting
factor binds to a promoter or enhancer. The principle technique is called gel retardation assay.
The principle underlining this procedure is that a DNA molecule exhibits a slower mobility when it
is bound by a protein than when it is naked. These experiments are performed on a
polyacrylamide gel under low ionic conditions.
Steps of gel retardation assay
- Identify a promoter region of interest.
- Make a crude nuclear protein extract from the developmental stage that the gene of interest is
- being expressed.
- Mix the promoter fragment of interest with the crude extract.
- Run the following samples:
- a. free promoter fragment
- b. promoter fragment + crude extract mixture
- c. crude extract + competitor + promoter fragment
Copyright © 1998. Phillip McClean