of other transcription factors also bind sequentially to form an initiation complex that
includes RNA polymerase, subsequent to which transcription is initiated. In addition
to the TATA box, aCAT box(consensus GGCCAATCT) is often located at about
80 bp, which is an important determinant of promoter efficiency. Manyupstream
promoter elements(UPEs) have been described that are either general in their action
or tissue (or gene) specific. GC elements that contain the sequence GGGCG may be
present at multiple sites and in either orientation and are often associated with
housekeeping genessuch as those encoding enzymes involved in general metabolism.
Some promoter sequence elements, such as the TATA box, are common to most genes,
while others may be specific to particular genes or classes of genes.
Of particular interest is a class of promoter first investigated in the virus SV40
and termed an enhancer. These sequences are distinguished from other promoter
sequences by their unique ability to function over several kilobases either upstream
(a)
Promoters
–35
TTGACA
–10
TATA
+1 Structural
gene
(b)
Upstream promoter elements
Variable
distance
enhancer
–80
CAAT or
G+C-rich
–35
TATA
+1 Structural
gene
3
(c)
TFII D
TFII A
TFII B
TFII E/F
RNA
pol II
–80
CAAT or
G+C-rich
–35
TATA
+1 Structural
gene
3
5
5
3
5
Fig. 5.15(a) Typical promoter elements found in a prokaryotic cell (e.g.E. coli). (b) Typical promoter
elements found in eukaryotic cells. (c) Generalised scheme of binding of transcription factors to the promoter
regions of eukaryotic cells. Following the binding of the transcription factors IID, IIA, IIB, IIE and IIF a
pre-initiation complex is formed. RNA polymerase II then binds to this complex and begins transcription
from the start pointþ1.
156 Molecular biology, bioinformatics and basic techniques