Characterization of KIAA0513, a novel signaling molecule that interacts with modulators of neuroplasticity, apoptosis, and the cytoskeleton

KIAA0513 was previously identified as upregulated in the dorsolateral prefrontal cortex of subjects with schizophrenia by microarray analysis. In the present study, the differential expression in the schizophrenic subjects was confirmed by quantitative RT-PCR. The limited homology to proteins of kno...

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Published inBrain research Vol. 1121; no. 1; pp. 1 - 11
Main Authors Lauriat, Tara L., Dracheva, Stella, Kremerskothen, Joachim, Duning, Kerstin, Haroutunian, Vahram, Buxbaum, Joseph D., Hyde, Thomas M., Kleinman, Joel E., Alison McInnes, L.
Format Journal Article
LanguageEnglish
Published London Elsevier B.V 22.11.2006
Amsterdam Elsevier
New York, NY
Subjects
Online AccessGet full text
ISSN0006-8993
1872-6240
DOI10.1016/j.brainres.2006.08.099

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Abstract KIAA0513 was previously identified as upregulated in the dorsolateral prefrontal cortex of subjects with schizophrenia by microarray analysis. In the present study, the differential expression in the schizophrenic subjects was confirmed by quantitative RT-PCR. The limited homology to proteins of known function and lack of functional domains in the encoded protein have made it difficult to predict a function for KIAA0513. We used in situ hybridization, RNA blots, western blots, and immunocytochemistry to examine KIAA0513 expression in normal brain and peripheral tissues. The gene is ubiquitously expressed but is enriched in the brain, particularly in the cerebellum. Finally, interacting proteins were identified using a yeast two-hybrid screen to functionally characterize the protein. KIAA0513 interacts with KIBRA, HAX-1, and INTS4, which also interact with proteins involved in neuroplasticity, apoptosis, and cytoskeletal regulation. Therefore, KIAA0513 is likely to be involved in signaling pathways related to these processes.
AbstractList KIAA0513 was previously identified as upregulated in the dorsolateral prefrontal cortex of subjects with schizophrenia by microarray analysis. In the present study, the differential expression in the schizophrenic subjects was confirmed by quantitative RT-PCR. The limited homology to proteins of known function and lack of functional domains in the encoded protein have made it difficult to predict a function for KIAA0513. We used in situ hybridization, RNA blots, western blots, and immunocytochemistry to examine KIAA0513 expression in normal brain and peripheral tissues. The gene is ubiquitously expressed but is enriched in the brain, particularly in the cerebellum. Finally, interacting proteins were identified using a yeast two-hybrid screen to functionally characterize the protein. KIAA0513 interacts with KIBRA, HAX-1, and INTS4, which also interact with proteins involved in neuroplasticity, apoptosis, and cytoskeletal regulation. Therefore, KIAA0513 is likely to be involved in signaling pathways related to these processes.
KIAA0513 was previously identified as upregulated in the dorsolateral prefrontal cortex of subjects with schizophrenia by microarray analysis. In the present study, the differential expression in the schizophrenic subjects was confirmed by quantitative RT-PCR. The limited homology to proteins of known function and lack of functional domains in the encoded protein have made it difficult to predict a function for KIAA0513. We used in situ hybridization, RNA blots, western blots, and immunocytochemistry to examine KIAA0513 expression in normal brain and peripheral tissues. The gene is ubiquitously expressed but is enriched in the brain, particularly in the cerebellum. Finally, interacting proteins were identified using a yeast two-hybrid screen to functionally characterize the protein. KIAA0513 interacts with KIBRA, HAX-1, and INTS4, which also interact with proteins involved in neuroplasticity, apoptosis, and cytoskeletal regulation. Therefore, KIAA0513 is likely to be involved in signaling pathways related to these processes. Disorders-Fourth Edition Chloride /5-Bromo-4-Chloro-3'-Indolyphosphate p-Toluidine domain protein
KIAA0513 was previously identified as upregulated in the dorsolateral prefrontal cortex of subjects with schizophrenia by microarray analysis. In the present study, the differential expression in the schizophrenic subjects was confirmed by quantitative RT-PCR. The limited homology to proteins of known function and lack of functional domains in the encoded protein have made it difficult to predict a function for KIAA0513. We used in situ hybridization, RNA blots, western blots, and immunocytochemistry to examine KIAA0513 expression in normal brain and peripheral tissues. The gene is ubiquitously expressed but is enriched in the brain, particularly in the cerebellum. Finally, interacting proteins were identified using a yeast two-hybrid screen to functionally characterize the protein. KIAA0513 interacts with KIBRA, HAX-1, and INTS4, which also interact with proteins involved in neuroplasticity, apoptosis, and cytoskeletal regulation. Therefore, KIAA0513 is likely to be involved in signaling pathways related to these processes.KIAA0513 was previously identified as upregulated in the dorsolateral prefrontal cortex of subjects with schizophrenia by microarray analysis. In the present study, the differential expression in the schizophrenic subjects was confirmed by quantitative RT-PCR. The limited homology to proteins of known function and lack of functional domains in the encoded protein have made it difficult to predict a function for KIAA0513. We used in situ hybridization, RNA blots, western blots, and immunocytochemistry to examine KIAA0513 expression in normal brain and peripheral tissues. The gene is ubiquitously expressed but is enriched in the brain, particularly in the cerebellum. Finally, interacting proteins were identified using a yeast two-hybrid screen to functionally characterize the protein. KIAA0513 interacts with KIBRA, HAX-1, and INTS4, which also interact with proteins involved in neuroplasticity, apoptosis, and cytoskeletal regulation. Therefore, KIAA0513 is likely to be involved in signaling pathways related to these processes.
Author Alison McInnes, L.
Kleinman, Joel E.
Duning, Kerstin
Lauriat, Tara L.
Buxbaum, Joseph D.
Kremerskothen, Joachim
Haroutunian, Vahram
Hyde, Thomas M.
Dracheva, Stella
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Issue 1
Keywords Cerebellum
DSM-IV
TRADD
WWC1
HRP
Schizophrenia
kDa
EGFP
ACTB
KIBRA
ANCOVA
BSA
DMEM
FITC
RT-PCR
NMDA
FADD
DISC1
B2M
DENN
PBS
SDS
DLPFC
N-terminal
Yeast two-hybrid
IP
DAPI
GST
PKC
Gene expression
PMI
NBT/BCIP
HAX-1
MADD
INTS4
GAPDH
MAP
MTE
Human
Central nervous system
Encephalon
Psychosis
Characterization
Polymerase chain reaction
Signal transduction
Cell death
Plasticity
Cytoskeleton
Apoptosis
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Snippet KIAA0513 was previously identified as upregulated in the dorsolateral prefrontal cortex of subjects with schizophrenia by microarray analysis. In the present...
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SubjectTerms Adult and adolescent clinical studies
Animals
Autopsy
Biological and medical sciences
Brain - physiology
Brain - physiopathology
Cerebellum
Cerebellum - metabolism
Cerebellum - pathology
DNA Primers
Female
Gene expression
Humans
In Situ Hybridization
KIBRA
Medical sciences
Nerve Tissue Proteins - genetics
Nerve Tissue Proteins - physiology
Nuclear Proteins - genetics
Nuclear Proteins - physiology
Oligonucleotide Array Sequence Analysis
Prefrontal Cortex - metabolism
Prefrontal Cortex - pathology
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Psychoses
Rats
Rats, Sprague-Dawley
Reverse Transcriptase Polymerase Chain Reaction
RNA - genetics
RNA - isolation & purification
RNA, Messenger - genetics
RT-PCR
Schizophrenia
Schizophrenia - genetics
Signal Transduction
Yeast two-hybrid
Title Characterization of KIAA0513, a novel signaling molecule that interacts with modulators of neuroplasticity, apoptosis, and the cytoskeleton
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0006899306026035
https://dx.doi.org/10.1016/j.brainres.2006.08.099
https://www.ncbi.nlm.nih.gov/pubmed/17010949
https://www.proquest.com/docview/19509865
https://www.proquest.com/docview/68143666
Volume 1121
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