The development of indirect flight muscle innervation in Drosophila melanogaster

Development ◽  
1993 ◽  
Vol 118 (1) ◽  
pp. 215-227 ◽  
Author(s):  
J. Fernandes ◽  
K. VijayRaghavan
Keyword(s):  
Muscle Development ◽  
Flight Muscle ◽  
Neuromuscular Junctions ◽  
Indirect Flight Muscle ◽  
Larval Life ◽  
Spatial And Temporal Patterns ◽  
Muscle Innervation ◽  
Flight Muscles ◽  
Nerve Muscle ◽  
Longitudinal Muscles

We have examined the development of innervation to the indirect flight muscles of Drosophila. During metamorphosis, the larval intersegmental nerve of the mesothorax is remodelled to innervate the dorsal longitudinal muscles and two of the dorsoventral muscles. Another modified larval nerve innervates the remaining dorsoventral muscle. The dorsal longitudinal muscles develop using modified larval muscles as templates while dorsoventral muscles develop without the use of such templates. The development of innervation to the two groups of indirect flight muscles differs in spatial and temporal patterns, which may reflect the different ways in which these muscles develop. The identification of myoblasts associated with thoracic nerves during larval life and the association of migrating myoblasts with nerves during metamorphosis indicate the existence of nerve-muscle interactions during indirect flight muscle development. In addition, the developing pattern of axonal branching suggests a role for the target muscles in respecifying neuromuscular junctions during metamorphosis.

Nerve-muscle interactions during flight muscle development in Drosophila

Development ◽  
1998 ◽  
Vol 125 (9) ◽  
pp. 1769-1779 ◽  
Author(s):  
J.J. Fernandes ◽  
H. Keshishian
Keyword(s):  
Muscle Development ◽  
Synapse Formation ◽  
Muscle Fibers ◽  
Developmental State ◽  
Fiber Formation ◽  
Absolute Dependence ◽  
Flight Muscles ◽  
Nerve Muscle ◽  
Longitudinal Muscles ◽  
Primary Motoneuron

During Drosophila pupal metamorphosis, the motoneurons and muscles differentiate synchronously, providing an opportunity for extensive intercellular regulation during synapse formation. We examined the existence of such interactions by developmentally delaying or permanently eliminating synaptic partners during the formation of indirect flight muscles. When we experimentally delayed muscle development, we found that although adult-specific primary motoneuron branching still occurred, the higher order (synaptic) branching was suspended until the delayed muscle fibers reached a favourable developmental state. In reciprocal experiments we found that denervation caused a decrease in the myoblast pool. Furthermore, the formation of certain muscle fibers (dorsoventral muscles) was specifically blocked. Exceptions were the adult muscles that use larval muscle fibers as myoblast fusion targets (dorsal longitudinal muscles). However, when these muscles were experimentally compelled to develop without their larval precursors, they showed an absolute dependence on the motoneurons for their formation. These data show that the size of the myoblast pool and early events in fiber formation depend on the presence of the nerve, and that, conversely, peripheral arbor development and synaptogenesis is closely synchronized with the developmental state of the muscle.

scholarly journals Flying High—Muscle-Specific Underreplication in Drosophila

Genes ◽  
2020 ◽  
Vol 11 (3) ◽  
pp. 246 ◽  
Author(s):  
J. Spencer Johnston ◽  
Mary E. Zapalac ◽  
Carl E. Hjelmen
Keyword(s):  
Flow Cytometry ◽  
Dna Synthesis ◽  
Salivary Glands ◽  
Genome Size ◽  
Flight Muscle ◽  
S Phase ◽  
The Other ◽  
Tissue Type ◽  
Flight Muscles ◽  
Longitudinal Muscles

Drosophila underreplicate the DNA of thoracic nuclei, stalling during S phase at a point that is proportional to the total genome size in each species. In polytene tissues, such as the Drosophila salivary glands, all of the nuclei initiate multiple rounds of DNA synthesis and underreplicate. Yet, only half of the nuclei isolated from the thorax stall; the other half do not initiate S phase. Our question was, why half? To address this question, we use flow cytometry to compare underreplication phenotypes between thoracic tissues. When individual thoracic tissues are dissected and the proportion of stalled DNA synthesis is scored in each tissue type, we find that underreplication occurs in the indirect flight muscle, with the majority of underreplicated nuclei in the dorsal longitudinal muscles (DLM). Half of the DNA in the DLM nuclei stall at S phase between the unreplicated G0 and fully replicated G1. The dorsal ventral flight muscle provides the other source of underreplication, and yet, there, the replication stall point is earlier (less DNA replicated), and the endocycle is initiated. The differences in underreplication and ploidy in the indirect flight muscles provide a new tool to study heterochromatin, underreplication and endocycle control.

Twist and Notch negatively regulate adult muscle differentiation in Drosophila

Development ◽  
1998 ◽  
Vol 125 (8) ◽  
pp. 1361-1369 ◽  
Author(s):  
S. Anant ◽  
S. Roy ◽  
K. Vijay Raghavan
Keyword(s):  
Cell Fate ◽  
Muscle Development ◽  
Flight Muscle ◽  
Mutant Phenotype ◽  
Indirect Flight Muscle ◽  
Adult Muscle ◽  
Drosophila Embryogenesis ◽  
Twist Expression ◽  
Somatic Muscles

Twist is required in Drosophila embryogenesis for mesodermal specification and cell-fate choice. We have examined the role of Twist and Notch during adult indirect flight muscle development. Reduction in levels of Twist leads to abnormal myogenesis. Notch reduction causes a similar mutant phenotype and reduces Twist levels. Conversely, persistent expression, in myoblasts, of activated Notch causes continued twist expression and failure of differentiation as assayed by myosin expression. The gain-of-function phenotype of Notch is very similar to that seen upon persistent twist expression. These results point to a relationship between Notch function and twist regulation during indirect flight muscle development and show that decline in Twist levels is a requirement for the differentiation of these muscles, unlike the somatic muscles of the embryo.

scholarly journals Roles of the troponin isoforms during indirect flight muscle development in Drosophila

2014 ◽  
Vol 93 (2) ◽  
pp. 379-388 ◽  
Author(s):  
SALAM HEROJEET SINGH ◽  
PRABODH KUMAR ◽  
NALLUR B. RAMACHANDRA ◽  
UPENDRA NONGTHOMBA
Keyword(s):  
Muscle Development ◽  
Flight Muscle ◽  
Indirect Flight Muscle

scholarly journals THE ORGANIZATION OF FLIGHT MUSCLE IN AN APHID, MEGOURA VICIAE (HOMOPTERA)

1965 ◽  
Vol 27 (2) ◽  
pp. 379-393 ◽  
Author(s):  
David S. Smith
Keyword(s):  
Plasma Membrane ◽  
Sarcoplasmic Reticulum ◽  
Cell Surface ◽  
Flight Muscle ◽  
Muscle Cells ◽  
Indirect Flight Muscle ◽  
Megoura Viciae ◽  
Flight Muscles ◽  
High Degree ◽  
T System

The organization of the indirect flight muscle of an aphid (Hemiptera-Homoptera) is described. The fibers of this muscle contain an extensive though irregularly disposed complement of T system tubules, derived as open invaginations from the cell surface and from the plasma membrane sheaths accompanying the tracheoles within the fiber. The sarcoplasmic reticulum is reduced to small vesicles applied to the T system surfaces, the intermembrane gap being traversed by blocks of electron-opaque material resembling that of septate desmosomes. The form and distribution of the T system and sarcoplasmic reticulum membranes in flight muscles of representatives of the major insect orders is described, and the extreme reduction of the reticulum cisternae in all asynchronous fibers (to which group the aphid flight muscle probably belongs), and the high degree of their development in synchronous fibers is documented and discussed in terms of the contraction physiology of these muscle cells.

ERECT WING, the Drosophila member of a family of DNA binding proteins is required in imaginal myoblasts for flight muscle development

Development ◽  
1996 ◽  
Vol 122 (1) ◽  
pp. 31-39 ◽  
Author(s):  
S. DeSimone ◽  
C. Coelho ◽  
S. Roy ◽  
K. VijayRaghavan ◽  
K. White
Keyword(s):  
Dna Binding ◽  
Muscle Development ◽  
Flight Muscle ◽  
Regulatory Gene ◽  
Fruit Fly ◽  
Postembryonic Development ◽  
Loss Of Function ◽  
Puparium Formation ◽  
Flight Muscles ◽  
First Time

The erect wing locus of the fruit fly Drosophila melanogaster encodes a protein, EWG, that shares extensive homology with the P3A2 DNA binding protein of sea urchin and a recently identified mammalian transcription factor. Loss-of-function erect wing alleles result in embryonic lethality. Viable alleles of erect wing cause severe abnormalities of the indirect flight muscles. We have analyzed the spatial pattern of erect wing expression in the developing indirect flight muscles during postembryonic development. EWG is detected, 10 hours after puparium formation, in myoblasts that will form the indirect flight muscles. The early events of muscle development are normal in ewg mutants. However, a few hours after the onset of erect wing expression in myoblasts, defects are seen in the developing indirect flight muscles which subsequently degenerate. We present results that show that the normal development of the indirect flight muscles requires erect wing expression in the progenitor myoblasts themselves. Finally, we examine the role of target muscles in the arborization of motor axons by studying the developing innervation to the flight muscle in erect wing mutants. Our study demonstrates, for the first time, a role for a regulatory gene expressed in imaginal myoblasts in Drosophila.

scholarly journals Neuromuscular Junctions in Flight and Tymbal Muscles of the Cicada

1958 ◽  
Vol 4 (3) ◽  
pp. 251-256 ◽  
Author(s):  
George A. Edwards ◽  
Helmut Ruska ◽  
Étienne de Harven
Keyword(s):  
Endoplasmic Reticulum ◽  
Neuromuscular Junction ◽  
Muscle Fiber ◽  
High Frequency ◽  
Plasma Membranes ◽  
Flight Muscle ◽  
Neuromuscular Junctions ◽  
Muscle Fibers ◽  
Membrane System ◽  
Indirect Flight Muscle

The tymbal muscle fiber in the cicada closely resembles the indirect flight muscle fiber in its structural detail. We agree with other authors that the tymbal muscle is a modified indirect flight muscle. The peripheral nerve branches to the tymbal and flight muscle fibers are similar to those in the wasp leg. The axon is loosely mantled by irregular turns of the mesaxon, enclosing cytoplasm. The nerve is therefore a tunicated nerve. The neuromuscular junction in the high frequency muscle fibers shows direct apposition of plasma membranes of axon and muscle fiber, large numbers of mitochondria and synaptic vesicles in the axon, and concentrations of mitochondria, aposynaptic granules, and endoplasmic reticulum in the postsynaptic area of the muscle fiber. Of special interest is the multitude of intracellular, opposing membranes in the postsynaptic area. They form laminated stacks and whorls, vesicles, cysternae, and tubules. They occasionally show continuity with the plasma membrane, the outer nuclear envelope, and the circumfibrillar endoplasmic reticulum. The membrane system in this area is designated "rete synapticum." It is believed to add to the electrical capacity of the neuromuscular junction, to serve in transmission of potentials, and possibly is the site of the oscillating mechanism in high-frequency muscle fibers.

scholarly journals Thin filaments elongate from their pointed ends during myofibril assembly in Drosophila indirect flight muscle

2001 ◽  
Vol 155 (6) ◽  
pp. 1043-1054 ◽  
Author(s):  
Michelle Mardahl-Dumesnil ◽  
Velia M. Fowler
Keyword(s):  
Thin Filament ◽  
Muscle Development ◽  
Striated Muscle ◽  
Flight Muscle ◽  
De Novo ◽  
Indirect Flight Muscle ◽  
Actin Dynamics ◽  
Thin Filaments ◽  
End Capping ◽  
Pointed End

Tropomodulin (Tmod) is an actin pointed-end capping protein that regulates actin dynamics at thin filament pointed ends in striated muscle. Although pointed-end capping by Tmod controls thin filament lengths in assembled myofibrils, its role in length specification during de novo myofibril assembly is not established. We used the Drosophila Tmod homologue, sanpodo (spdo), to investigate Tmod's function during muscle development in the indirect flight muscle. SPDO was associated with the pointed ends of elongating thin filaments throughout myofibril assembly. Transient overexpression of SPDO during myofibril assembly irreversibly arrested elongation of preexisting thin filaments. However, the lengths of thin filaments assembled after SPDO levels had declined were normal. Flies with a preponderance of abnormally short thin filaments were unable to fly. We conclude that: (a) thin filaments elongate from their pointed ends during myofibril assembly; (b) pointed ends are dynamically capped at endogenous levels of SPDO so as to allow elongation; (c) a transient increase in SPDO levels during myofibril assembly converts SPDO from a dynamic to a permanent cap; and (d) developmental regulation of pointed-end capping during myofibril assembly is crucial for specification of final thin filament lengths, myofibril structure, and muscle function.

scholarly journals Correction to: Roles of the troponin isoforms during indirect flight muscle development in Drosophila

2019 ◽  
Vol 98 (5) ◽  
Author(s):  
Salam Herojeet Singh ◽  
Prabodh Kumar ◽  
Nallur B. Ramachandra ◽  
Upendra Nongthomba
Keyword(s):  
Muscle Development ◽  
Flight Muscle ◽  
Indirect Flight Muscle
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