TY - CHAP
T1 - Mitochondrial DNA Transport in Drosophila Neurons
AU - Bateman, Joseph
N1 - Funding Information:
Work in this area in my laboratory is currently funded by grants from Alzheimer’s research UK (ARUK-IRG2017A-2), the NC3Rs (NC/V001884/1), and the MRC (MR/V013130/1). I thank the Wohl Cellular Imaging Centre at King’s College London for help with light microscopy.
Publisher Copyright:
© 2022, The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2022/4/16
Y1 - 2022/4/16
N2 - Mitochondria are essential organelles that generate energy and play vital roles in cellular metabolism. The small circular mitochondrial genome encodes key components of the mitochondrial respiratory apparatus. Depletion of, or mutations in mitochondrial DNA (mtDNA) cause mitochondrial dysfunction and disease. mtDNA is packaged into nucleoids, which are transported throughout the cell within mitochondria. Efficient transport of nucleoids is essential in neurons, where mitochondrial function is required locally at synapses. Here I describe methods for visualization of nucleoids in Drosophila neurons using a GFP fusion of the mitochondrial transcription factor TFAM. TFAM-GFP, together with mCherry-labeled mitochondria, was used to visualize nucleoids in fixed larval segmental nerves. I also describe how these tools can be used for live imaging of nucleoid dynamics. Using Drosophila as a model system, these methods will enable further characterization and analysis of nucleoid dynamics in neurons.
AB - Mitochondria are essential organelles that generate energy and play vital roles in cellular metabolism. The small circular mitochondrial genome encodes key components of the mitochondrial respiratory apparatus. Depletion of, or mutations in mitochondrial DNA (mtDNA) cause mitochondrial dysfunction and disease. mtDNA is packaged into nucleoids, which are transported throughout the cell within mitochondria. Efficient transport of nucleoids is essential in neurons, where mitochondrial function is required locally at synapses. Here I describe methods for visualization of nucleoids in Drosophila neurons using a GFP fusion of the mitochondrial transcription factor TFAM. TFAM-GFP, together with mCherry-labeled mitochondria, was used to visualize nucleoids in fixed larval segmental nerves. I also describe how these tools can be used for live imaging of nucleoid dynamics. Using Drosophila as a model system, these methods will enable further characterization and analysis of nucleoid dynamics in neurons.
UR - http://www.scopus.com/inward/record.url?scp=85128073163&partnerID=8YFLogxK
U2 - 10.1007/978-1-0716-1990-2_21
DO - 10.1007/978-1-0716-1990-2_21
M3 - Chapter
VL - 2431
T3 - Methods in Molecular Biology
SP - 409
EP - 416
BT - Methods in Molecular Biology
ER -