TY - JOUR
T1 - The neuronal nicotinic acetylcholine receptor α2 subunit gene promoter is activated by the Brn-3b POU family transcription factor and not by Brn-3a or Brn-3c
AU - Milton, Nathaniel G.N.
AU - Bessis, Alain
AU - Changeux, Jean Pierre
AU - Latchman, David S.
PY - 1995/6/23
Y1 - 1995/6/23
N2 - The regulatory region of the neuronal nicotinic acetylcholine receptor α2 subunit gene, which contains six copies of the octamer-related sequence CCCCATGCAAT, is activated by the Brn-3b POU family transcription factor but not by the closely related factors Brn-3a and Brn-3c. This effect is in contrast to the previously documented inhibitory effect of Brn-3b on octamer- containing promoters that are activated by Brn-3a and Brn-3c. Activation of the α2 gene by Brn-3b requires that both the POU domain and other N-terminal sequences are derived from Brn-3b and is dependent on the intactness of the α2 gene regulatory region, being lost in truncated derivatives containing one, two, or four copies of the octamer-related sequence. Surprisingly, however, these truncated derivatives are activated by Bru-3c. These effects are discussed in terms of both the influence of the target sequence and its context in the promoter on activation by the various forms of Brn-3 as well as of the processes that restrict expression of the α2 subunit gene to a few cells in the nervous system.
AB - The regulatory region of the neuronal nicotinic acetylcholine receptor α2 subunit gene, which contains six copies of the octamer-related sequence CCCCATGCAAT, is activated by the Brn-3b POU family transcription factor but not by the closely related factors Brn-3a and Brn-3c. This effect is in contrast to the previously documented inhibitory effect of Brn-3b on octamer- containing promoters that are activated by Brn-3a and Brn-3c. Activation of the α2 gene by Brn-3b requires that both the POU domain and other N-terminal sequences are derived from Brn-3b and is dependent on the intactness of the α2 gene regulatory region, being lost in truncated derivatives containing one, two, or four copies of the octamer-related sequence. Surprisingly, however, these truncated derivatives are activated by Bru-3c. These effects are discussed in terms of both the influence of the target sequence and its context in the promoter on activation by the various forms of Brn-3 as well as of the processes that restrict expression of the α2 subunit gene to a few cells in the nervous system.
UR - http://www.scopus.com/inward/record.url?scp=0029036898&partnerID=8YFLogxK
U2 - 10.1074/jbc.270.25.15143
DO - 10.1074/jbc.270.25.15143
M3 - Article
C2 - 7797498
AN - SCOPUS:0029036898
SN - 0021-9258
VL - 270
SP - 15143
EP - 15147
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 25
ER -