TY - JOUR
T1 - Binding affinities and cooperative interactions with bHLH activators delimit threshold responses to the dorsal gradient morphogen
AU - Jiang, Jin
AU - Levine, Michael
N1 - Funding Information:
We thank Ct. Zhou for technical assistance and G. Struhl, E. Davidson, S. Small, J. Kadonaga, C. Murre, and J. Posakonyfor critically reading the manuscript. We also thank P. Powell and J. Posakony for the glutathione S-transferase-T4 plasmid used in Figure 7. This work was funded by a grant from the National Institutes of Health (GM46638).
PY - 1993/3/12
Y1 - 1993/3/12
N2 - The dorsal (dl) morphogen gradient initiates the formation of the mesoderm, neuroectoderm, and dorsal ectoderm by setting different limits of regulatory gene expression along the dorsoventral axis of the early Drosophila embryo. In this paper, we show that low affinity dl-binding sites restrict target gene expression to the ventralmost regions (presumptive mesoderm), where there are peak levels of dl, while high affinity sites permit expression in ventrolateral regions (mesoderm and mesectoderm) containing intermediate levels of the morphogen. Activation by low levels of dl in lateral regions (the presumptive neuroectoderm) depends on cooperative DNA binding interactions between dl and bHLH proteins. The snall repressor blocks this interaction and restricts expression to the neuroectoderm. We discuss how enhancers serve as templates to bring weakly interacting regulatory factors into close proximity so that they can function combinatorially to activate and repress transcription.
AB - The dorsal (dl) morphogen gradient initiates the formation of the mesoderm, neuroectoderm, and dorsal ectoderm by setting different limits of regulatory gene expression along the dorsoventral axis of the early Drosophila embryo. In this paper, we show that low affinity dl-binding sites restrict target gene expression to the ventralmost regions (presumptive mesoderm), where there are peak levels of dl, while high affinity sites permit expression in ventrolateral regions (mesoderm and mesectoderm) containing intermediate levels of the morphogen. Activation by low levels of dl in lateral regions (the presumptive neuroectoderm) depends on cooperative DNA binding interactions between dl and bHLH proteins. The snall repressor blocks this interaction and restricts expression to the neuroectoderm. We discuss how enhancers serve as templates to bring weakly interacting regulatory factors into close proximity so that they can function combinatorially to activate and repress transcription.
UR - http://www.scopus.com/inward/record.url?scp=0027511507&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0027511507&partnerID=8YFLogxK
U2 - 10.1016/0092-8674(93)90402-C
DO - 10.1016/0092-8674(93)90402-C
M3 - Article
C2 - 8453668
AN - SCOPUS:0027511507
SN - 0092-8674
VL - 72
SP - 741
EP - 752
JO - Cell
JF - Cell
IS - 5
ER -