TY - JOUR
T1 - Cell type-specific transcriptional regulation of the drosophila FMRFamide neuropeptide gene
AU - Schneider, Lynne E.
AU - Roberts, Marie S.
AU - Taghert, Paul H.
N1 - Funding Information:
We wish to thank Carl Thummel, Vince Pirrotta, Yash Hiromi, and Steve Crews for sending vectors; John Majors and Jay Hirsh for advice; and John Merlie, Martha O’Brien, Karen O’Malley, Josh Sanes, and Dusan Zitnan for their comments on the manuscript. This work was supported by a grant from the National Institutes of Health (#21749) to P. H. T.
PY - 1993/2
Y1 - 1993/2
N2 - We have used IacZ reporter gene constructs to study the promoter/enhancer regions of the Drosophila FMRFamide neuropeptide gene in germ line transformants. FMRFamide is normally expressed ∼60 diverse neurons of the larval CNS that represent ∼15 distinct cell types. An 8 kb FMRFamide DNA fragment (including 5 kb of 5′ upstream sequence) was sufficient to direct a pattern of IacZ expression that mimicked nearly all spatial aspects of the normal pattern. This result indicates that the cell-specific regulation of FMRFamide expression is largely generated by transcriptional mechanisms. Reporter gene expression was lost from selected cell types when smaller fragments were tested, suggesting that multiple control regions are included in the FMRFamide promoter. One region (a 300 by fragment from -476 to -162) acted as an enhancer for 1 of the ∼15 FMRFamide-positive cell types, the OL2 neurons. These results suggest that, in the mature nervous system, the complex pattern of FMRFamide neuropeptide gene expression derives from the activity of discrete, cell type-specific enhancers that are independently regulated.
AB - We have used IacZ reporter gene constructs to study the promoter/enhancer regions of the Drosophila FMRFamide neuropeptide gene in germ line transformants. FMRFamide is normally expressed ∼60 diverse neurons of the larval CNS that represent ∼15 distinct cell types. An 8 kb FMRFamide DNA fragment (including 5 kb of 5′ upstream sequence) was sufficient to direct a pattern of IacZ expression that mimicked nearly all spatial aspects of the normal pattern. This result indicates that the cell-specific regulation of FMRFamide expression is largely generated by transcriptional mechanisms. Reporter gene expression was lost from selected cell types when smaller fragments were tested, suggesting that multiple control regions are included in the FMRFamide promoter. One region (a 300 by fragment from -476 to -162) acted as an enhancer for 1 of the ∼15 FMRFamide-positive cell types, the OL2 neurons. These results suggest that, in the mature nervous system, the complex pattern of FMRFamide neuropeptide gene expression derives from the activity of discrete, cell type-specific enhancers that are independently regulated.
UR - http://www.scopus.com/inward/record.url?scp=0027465482&partnerID=8YFLogxK
U2 - 10.1016/0896-6273(93)90318-L
DO - 10.1016/0896-6273(93)90318-L
M3 - Article
C2 - 8439413
AN - SCOPUS:0027465482
SN - 0896-6273
VL - 10
SP - 279
EP - 291
JO - Neuron
JF - Neuron
IS - 2
ER -