 |
Previous Article | Next Article 
The Journal of Neuroscience, September 15, 1998, 18(18):7138-7151
Functional Redundancy of FMRFamide-Related Peptides at the
Drosophila Larval Neuromuscular Junction
Randall S.
Hewes1,
Eric
C
Snowdeal III1,
Minoru
Saitoe2, and
Paul H.
Taghert1
1 Department of Anatomy and Neurobiology, Washington
University School of Medicine, St. Louis, Missouri 63110, and
2 Cold Spring Harbor Laboratory, Cold Spring Harbor, New
York 11724
The Drosophila FMRFamide gene encodes multiple
FMRFamide-related peptides. These peptides are expressed by
neurosecretory cells and may be released into the blood to act as
neurohormones. We analyzed the effects of eight of these peptides on
nerve-stimulated contraction (twitch tension) of
Drosophila larval body-wall muscles. Seven of the
peptides strongly enhanced twitch tension, and one of the peptides was
inactive. Their targets were distributed widely throughout the somatic
musculature. The effects of one peptide, DPKQDFMRFamide, were
unchanged after the onset of metamorphosis. The seven active peptides
showed similar dose-response curves. Each had a threshold
concentration near 1 nM, and the EC50 for each
peptide was ~40 nM. At concentrations <0.1
µM, the responses to each of the seven excitatory
peptides followed a time course that matched the fluctuations of the
peptide concentration in the bath. At higher concentrations, twitch
tension remained elevated for 5-10 min or more after wash-out of the
peptide. When the peptides were presented as mixtures predicted by
their stoichiometric ratios in the dFMRFamide propeptide, the effects
were additive, and there were no detectable higher-order interactions
among them. One peptide was tested and found to enhance synaptic
transmission. At 0.1 µM, DPKQDFMRFamide increased the
amplitude of the excitatory junctional current to 151% of baseline
within 3 min. Together, these results indicate that the products of the
Drosophila FMRFamide gene function as neurohormones to
modulate the strength of contraction at the larval neuromuscular
junction. In this role these seven peptides appear to be functionally
redundant.
Key words:
Drosophila melanogaster; FMRFamide; neuromuscular junction; NMJ; muscle; neuropeptide; peptide hormone; propeptide; synapse
Copyright © 1998 Society for Neuroscience 0270-6474/98/18187138-14$05.00/0
This article has been cited by other articles:

|
 |

|
 |
 
K. T. Eade and D. W. Allan
Neuronal Phenotype in the Mature Nervous System Is Maintained by Persistent Retrograde Bone Morphogenetic Protein Signaling
J. Neurosci.,
March 25, 2009;
29(12):
3852 - 3864.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
E. C. Johnson, L. M. Bohn, L. S. Barak, R. T. Birse, D. R. Nassel, M. G. Caron, and P. H. Taghert
Identification of Drosophila Neuropeptide Receptors by G Protein-coupled Receptors-{beta}-Arrestin2 Interactions
J. Biol. Chem.,
December 26, 2003;
278(52):
52172 - 52178.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
G. Marques, T. E. Haerry, M. L. Crotty, M. Xue, B. Zhang, and M. B. O'Connor
Retrograde Gbb signaling through the Bmp type 2 receptor Wishful Thinking regulates systemic FMRFa expression in Drosophila
Development,
November 15, 2003;
130(22):
5457 - 5470.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
T. C. Jacob and J. M . Kaplan
The EGL-21 Carboxypeptidase E Facilitates Acetylcholine Release at Caenorhabditis elegans Neuromuscular Junctions
J. Neurosci.,
March 15, 2003;
23(6):
2122 - 2130.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
T. Meeusen, I. Mertens, E. Clynen, G. Baggerman, R. Nichols, R. J. Nachman, R. Huybrechts, A. De Loof, and L. Schoofs
Identification in Drosophila melanogaster of the invertebrate G protein-coupled FMRFamide receptor
PNAS,
November 26, 2002;
99(24):
15363 - 15368.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
G. Cazzamali and C. J. P. Grimmelikhuijzen
Molecular cloning and functional expression of the first insect FMRFamide receptor
PNAS,
September 17, 2002;
99(19):
12073 - 12078.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
Y. Furukawa, K. Nakamaru, H. Wakayama, Y. Fujisawa, H. Minakata, S. Ohta, F. Morishita, O. Matsushima, L. Li, E. Romanova, et al.
The Enterins: A Novel Family of Neuropeptides Isolated from the Enteric Nervous System and CNS of Aplysia
J. Neurosci.,
October 15, 2001;
21(20):
8247 - 8261.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. Winther and D. Nassel
Intestinal peptides as circulating hormones: release of tachykinin-related peptide from the locust and cockroach midgut
J. Exp. Biol.,
January 4, 2001;
204(7):
1269 - 1280.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
Y. Fujisawa, Y. Furukawa, S. Ohta, T. A. Ellis, N. C. Dembrow, L. Li, P. D. Floyd, J. V. Sweedler, H. Minakata, K. Nakamaru, et al.
The Aplysia Mytilus Inhibitory Peptide-Related Peptides: Identification, Cloning, Processing, Distribution, and Action
J. Neurosci.,
November 1, 1999;
19(21):
9618 - 9634.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. R. Hwang, D. E. Siekhaus, R. S. Fuller, P. H. Taghert, and I. Lindberg
Interaction of Drosophila melanogaster Prohormone Convertase 2 and 7B2. INSECT CELL-SPECIFIC PROCESSING AND SECRETION
J. Biol. Chem.,
June 2, 2000;
275(23):
17886 - 17893.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|

|