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 in | Brain research Vol. 1121; no. 1; pp. 1 - 11 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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London
Elsevier B.V
22.11.2006
Amsterdam Elsevier New York, NY |
Subjects | |
Online Access | Get full text |
ISSN | 0006-8993 1872-6240 |
DOI | 10.1016/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. |
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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 |
Author_xml | – sequence: 1 givenname: Tara L. surname: Lauriat fullname: Lauriat, Tara L. organization: Department of Psychiatry, Mount Sinai School of Medicine, New York, NY, USA – sequence: 2 givenname: Stella surname: Dracheva fullname: Dracheva, Stella organization: Department of Psychiatry, Mount Sinai School of Medicine, New York, NY, USA – sequence: 3 givenname: Joachim surname: Kremerskothen fullname: Kremerskothen, Joachim organization: Department for Medicine, Division of Nephrology, University Clinics Muenster, Muenster, Germany – sequence: 4 givenname: Kerstin surname: Duning fullname: Duning, Kerstin organization: Department for Medicine, Division of Nephrology, University Clinics Muenster, Muenster, Germany – sequence: 5 givenname: Vahram surname: Haroutunian fullname: Haroutunian, Vahram organization: Department of Psychiatry, Mount Sinai School of Medicine, New York, NY, USA – sequence: 6 givenname: Joseph D. surname: Buxbaum fullname: Buxbaum, Joseph D. organization: Department of Psychiatry, Mount Sinai School of Medicine, New York, NY, USA – sequence: 7 givenname: Thomas M. surname: Hyde fullname: Hyde, Thomas M. organization: Clinical Brain Disorders Branch, National Institute of Mental Health, Bethesda, MD, USA – sequence: 8 givenname: Joel E. surname: Kleinman fullname: Kleinman, Joel E. organization: Clinical Brain Disorders Branch, National Institute of Mental Health, Bethesda, MD, USA – sequence: 9 givenname: L. surname: Alison McInnes fullname: Alison McInnes, L. email: alison.mcinnes@mssm.edu organization: Department of Psychiatry, Mount Sinai School of Medicine, New York, NY, USA |
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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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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 |
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