Dab2IP GTPase Activating Protein Regulates Dendrite Development and Synapse Number in Cerebellum

DOC-2/DAB-2 interacting protein (Dab2IP) is a GTPase activating protein that binds to Disabled-1, a cytosolic adapter protein involved in Reelin signaling and brain development. Dab2IP regulates PI3K-AKT signaling and is associated with metastatic prostate cancer, abdominal aortic aneurysms and coro...

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Published inPloS one Vol. 8; no. 1; p. e53635
Main Authors Qiao, Shuhong, Kim, Sun-Hong, Heck, Detlef, Goldowitz, Daniel, LeDoux, Mark S., Homayouni, Ramin
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 09.01.2013
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Abstract DOC-2/DAB-2 interacting protein (Dab2IP) is a GTPase activating protein that binds to Disabled-1, a cytosolic adapter protein involved in Reelin signaling and brain development. Dab2IP regulates PI3K-AKT signaling and is associated with metastatic prostate cancer, abdominal aortic aneurysms and coronary heart disease. To date, the physiological function of Dab2IP in the nervous system, where it is highly expressed, is relatively unknown. In this study, we generated a mouse model with a targeted disruption of Dab2IP using a retrovirus gene trap strategy. Unlike reeler mice, Dab2IP knock-down mice did not exhibit severe ataxia or cerebellar hypoplasia. However, Dab2IP deficiency produced a number of cerebellar abnormalities such as a delay in the development of Purkinje cell (PC) dendrites, a decrease in the parallel fiber synaptic marker VGluT1, and an increase in the climbing fiber synaptic marker VGluT2. These findings demonstrate for the first time that Dab2IP plays an important role in dendrite development and regulates the number of synapses in the cerebellum.
AbstractList DOC-2/DAB-2 interacting protein (Dab2IP) is a GTPase activating protein that binds to Disabled-1, a cytosolic adapter protein involved in Reelin signaling and brain development. Dab2IP regulates PI3K-AKT signaling and is associated with metastatic prostate cancer, abdominal aortic aneurysms and coronary heart disease. To date, the physiological function of Dab2IP in the nervous system, where it is highly expressed, is relatively unknown. In this study, we generated a mouse model with a targeted disruption of Dab2IP using a retrovirus gene trap strategy. Unlike reeler mice, Dab2IP knock-down mice did not exhibit severe ataxia or cerebellar hypoplasia. However, Dab2IP deficiency produced a number of cerebellar abnormalities such as a delay in the development of Purkinje cell (PC) dendrites, a decrease in the parallel fiber synaptic marker VGluT1, and an increase in the climbing fiber synaptic marker VGluT2. These findings demonstrate for the first time that Dab2IP plays an important role in dendrite development and regulates the number of synapses in the cerebellum.
DOC-2/DAB-2 interacting protein (Dab2IP) is a GTPase activating protein that binds to Disabled-1, a cytosolic adapter protein involved in Reelin signaling and brain development. Dab2IP regulates PI3K-AKT signaling and is associated with metastatic prostate cancer, abdominal aortic aneurysms and coronary heart disease. To date, the physiological function of Dab2IP in the nervous system, where it is highly expressed, is relatively unknown. In this study, we generated a mouse model with a targeted disruption of Dab2IP using a retrovirus gene trap strategy. Unlike reeler mice, Dab2IP knock-down mice did not exhibit severe ataxia or cerebellar hypoplasia. However, Dab2IP deficiency produced a number of cerebellar abnormalities such as a delay in the development of Purkinje cell (PC) dendrites, a decrease in the parallel fiber synaptic marker VGluT1, and an increase in the climbing fiber synaptic marker VGluT2. These findings demonstrate for the first time that Dab2IP plays an important role in dendrite development and regulates the number of synapses in the cerebellum.
DOC-2/DAB-2 interacting protein (Dab2IP) is a GTPase activating protein that binds to Disabled-1, a cytosolic adapter protein involved in Reelin signaling and brain development. Dab2IP regulates PI3K-AKT signaling and is associated with metastatic prostate cancer, abdominal aortic aneurysms and coronary heart disease. To date, the physiological function of Dab2IP in the nervous system, where it is highly expressed, is relatively unknown. In this study, we generated a mouse model with a targeted disruption of Dab2IP using a retrovirus gene trap strategy. Unlike reeler mice, Dab2IP knock-down mice did not exhibit severe ataxia or cerebellar hypoplasia. However, Dab2IP deficiency produced a number of cerebellar abnormalities such as a delay in the development of Purkinje cell (PC) dendrites, a decrease in the parallel fiber synaptic marker VGluT1, and an increase in the climbing fiber synaptic marker VGluT2. These findings demonstrate for the first time that Dab2IP plays an important role in dendrite development and regulates the number of synapses in the cerebellum.DOC-2/DAB-2 interacting protein (Dab2IP) is a GTPase activating protein that binds to Disabled-1, a cytosolic adapter protein involved in Reelin signaling and brain development. Dab2IP regulates PI3K-AKT signaling and is associated with metastatic prostate cancer, abdominal aortic aneurysms and coronary heart disease. To date, the physiological function of Dab2IP in the nervous system, where it is highly expressed, is relatively unknown. In this study, we generated a mouse model with a targeted disruption of Dab2IP using a retrovirus gene trap strategy. Unlike reeler mice, Dab2IP knock-down mice did not exhibit severe ataxia or cerebellar hypoplasia. However, Dab2IP deficiency produced a number of cerebellar abnormalities such as a delay in the development of Purkinje cell (PC) dendrites, a decrease in the parallel fiber synaptic marker VGluT1, and an increase in the climbing fiber synaptic marker VGluT2. These findings demonstrate for the first time that Dab2IP plays an important role in dendrite development and regulates the number of synapses in the cerebellum.
Audience Academic
Author Homayouni, Ramin
Goldowitz, Daniel
LeDoux, Mark S.
Kim, Sun-Hong
Qiao, Shuhong
Heck, Detlef
AuthorAffiliation 2 Department of Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, Tennessee, United States of America
1 Department of Biological Sciences, University of Memphis, Memphis, Tennessee, United States of America
3 Department of Neurology, University of Tennessee Health Science Center, Memphis, Tennessee, United States of America
University of Nebraska Medical Center, United States of America
AuthorAffiliation_xml – name: 3 Department of Neurology, University of Tennessee Health Science Center, Memphis, Tennessee, United States of America
– name: 2 Department of Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, Tennessee, United States of America
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Current address: Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore Maryland, United States of America
Competing Interests: The authors have declared that no competing interests exist.
Current address: Centre for Molecular Medicine and Therapeutics, Children and Family Research Institute, Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada
Conceived and designed the experiments: SQ S-HK RH. Performed the experiments: SQ SK. Analyzed the data: SQ S-HK DH MSL. Contributed reagents/materials/analysis tools: MSL DG DH RH. Wrote the paper: SQ S-KH MSL RH.
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Snippet DOC-2/DAB-2 interacting protein (Dab2IP) is a GTPase activating protein that binds to Disabled-1, a cytosolic adapter protein involved in Reelin signaling and...
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SubjectTerms 1-Phosphatidylinositol 3-kinase
Abnormalities
Adapter proteins
Adapters
AKT protein
Analysis
Aneurysm
Animals
Aorta
Apoptosis
Ataxia
Biology
Biomarkers - metabolism
Brain
Cancer metastasis
Cardiovascular disease
Cardiovascular diseases
Cerebellum
Cerebellum - cytology
Cerebellum - enzymology
Climbing
Coronary artery disease
Coronary heart disease
Dendrites
Dendrites - enzymology
Dietary fiber
Disabled-1 protein
Female
Gene Knockdown Techniques
Guanosine triphosphatases
Heart diseases
Hypoplasia
Kinases
Metastases
Mice
Mice, Inbred C57BL
Mossy Fibers, Hippocampal - enzymology
Nervous system
Neurobiology
Neurogenesis
Neurology
Neurons
Neurosciences
Physiological aspects
Prostate cancer
Protein binding
Protein Transport
Purkinje Cells - cytology
Purkinje Cells - enzymology
ras GTPase-Activating Proteins - deficiency
ras GTPase-Activating Proteins - metabolism
Reelin Protein
Regulation
Reproducibility of Results
Science
Signaling
Synapses
Synapses - enzymology
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Title Dab2IP GTPase Activating Protein Regulates Dendrite Development and Synapse Number in Cerebellum
URI https://www.ncbi.nlm.nih.gov/pubmed/23326475
https://www.proquest.com/docview/1289875692
https://www.proquest.com/docview/1273626066
https://pubmed.ncbi.nlm.nih.gov/PMC3541190
https://doaj.org/article/76e6625d826b4c15a8f01332f5a09840
http://dx.doi.org/10.1371/journal.pone.0053635
Volume 8
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