Changes in Brain Gene Expression Shared by Scrapie and Alzheimer Disease

We have isolated two recombinant cDNAs whose corresponding RNAs have an increased abundance in scrapie-infected hamster brain. DNA sequence analysis has shown that these two recombinants represent the genes for sulfated glycoprotein 2 and transferrin. The abundance of sulfated glycoprotein 2 RNA is...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 1989-09, Vol.86 (18), p.7260-7264
Hauptverfasser: Duguid, John R., Bohmont, Craig W., Liu, Ningai, Tourtellotte, Wallace W.
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container_end_page 7264
container_issue 18
container_start_page 7260
container_title Proceedings of the National Academy of Sciences - PNAS
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creator Duguid, John R.
Bohmont, Craig W.
Liu, Ningai
Tourtellotte, Wallace W.
description We have isolated two recombinant cDNAs whose corresponding RNAs have an increased abundance in scrapie-infected hamster brain. DNA sequence analysis has shown that these two recombinants represent the genes for sulfated glycoprotein 2 and transferrin. The abundance of sulfated glycoprotein 2 RNA is increased in hippocampus from patients with Alzheimer disease and Pick disease, whereas transferrin RNA is not strongly modulated in these conditions. Expression of two previously identified scrapie-modulated genes, encoding glial fibrillary acidic protein and metallothionein, is also increased in both of these neurodegenerative diseases.
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DNA sequence analysis has shown that these two recombinants represent the genes for sulfated glycoprotein 2 and transferrin. The abundance of sulfated glycoprotein 2 RNA is increased in hippocampus from patients with Alzheimer disease and Pick disease, whereas transferrin RNA is not strongly modulated in these conditions. 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DNA sequence analysis has shown that these two recombinants represent the genes for sulfated glycoprotein 2 and transferrin. The abundance of sulfated glycoprotein 2 RNA is increased in hippocampus from patients with Alzheimer disease and Pick disease, whereas transferrin RNA is not strongly modulated in these conditions. Expression of two previously identified scrapie-modulated genes, encoding glial fibrillary acidic protein and metallothionein, is also increased in both of these neurodegenerative diseases.</description><subject>Alzheimer Disease - genetics</subject><subject>Alzheimer Disease - metabolism</subject><subject>Alzheimer's disease</subject><subject>Alzheimers disease</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>brain</subject><subject>Brain - metabolism</subject><subject>Clusterin</subject><subject>Cricetinae</subject><subject>DNA</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Glial Fibrillary Acidic Protein - genetics</subject><subject>glycoproteins</subject><subject>Glycoproteins - genetics</subject><subject>Libraries</subject><subject>Messenger RNA</subject><subject>Metallothionein - genetics</subject><subject>Molecular and cellular biology</subject><subject>Molecular Chaperones</subject><subject>Molecular genetics</subject><subject>Molecular Sequence Data</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>Nervous system diseases</subject><subject>Neurodegenerative diseases</subject><subject>Nucleic acids</subject><subject>Rats</subject><subject>RNA</subject><subject>RNA, Messenger - genetics</subject><subject>Scrapie - genetics</subject><subject>Scrapie - metabolism</subject><subject>Sequence Homology, Nucleic Acid</subject><subject>Transcription, Genetic</subject><subject>transferrin</subject><subject>Transferrin - genetics</subject><subject>Transferrins</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkTtvFDEUhS0ECkugRkICTQNUs_H7UVCEJSRIkSgCteXx3Mk6mvVM7FmU8OvxaoeFNNDYxfnOvefqIPSS4CXBip2M0eWllkuil4pK_AgtCDakltzgx2iBMVW15pQ_Rc9yvsEYG6HxETqiSmOh8AJdrNYuXkOuQqw-Jlfec4hQnd2NCXIOQ6yu1i5BWzX31ZVPbgxQudhWp_3PNYQNpOpTyOAyPEdPOtdneDH_x-j757Nvq4v68uv5l9XpZe2F1lPNGsIbSZVoGy-U4Uy0TLpGeNwpwYGaRktHcUNlC9AYSggjCjvVeuM4EMGO0Yf93HHbbKD1EKfkejumsHHp3g4u2IdKDGt7Pfyw1GjMVPG_m_1puN1CnuwmZA997yIM22xV2clLlP-CJQtTWpkCnuxBn4acE3SHMATbXUl2V5LV0hJtdyUVx-u_bzjwcytFfzvrLnvXd8lFH_KfsYZxJQUt3JuZ2y34LT9Y9P6fgO22fT_B3VTIV3vyJk9DOqCMc07YL4b3uz4</recordid><startdate>19890901</startdate><enddate>19890901</enddate><creator>Duguid, John R.</creator><creator>Bohmont, Craig W.</creator><creator>Liu, Ningai</creator><creator>Tourtellotte, Wallace W.</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T3</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19890901</creationdate><title>Changes in Brain Gene Expression Shared by Scrapie and Alzheimer Disease</title><author>Duguid, John R. ; Bohmont, Craig W. ; Liu, Ningai ; Tourtellotte, Wallace W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c588t-3b14b6275dbc579435d36ab5c0f754e29b86a20b26deeb92113170a7dc9a4e153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Alzheimer Disease - genetics</topic><topic>Alzheimer Disease - metabolism</topic><topic>Alzheimer's disease</topic><topic>Alzheimers disease</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>brain</topic><topic>Brain - metabolism</topic><topic>Clusterin</topic><topic>Cricetinae</topic><topic>DNA</topic><topic>Fundamental and applied biological sciences. 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DNA sequence analysis has shown that these two recombinants represent the genes for sulfated glycoprotein 2 and transferrin. The abundance of sulfated glycoprotein 2 RNA is increased in hippocampus from patients with Alzheimer disease and Pick disease, whereas transferrin RNA is not strongly modulated in these conditions. Expression of two previously identified scrapie-modulated genes, encoding glial fibrillary acidic protein and metallothionein, is also increased in both of these neurodegenerative diseases.</abstract><cop>Washington, DC</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>2780570</pmid><doi>10.1073/pnas.86.18.7260</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
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subjects Alzheimer Disease - genetics
Alzheimer Disease - metabolism
Alzheimer's disease
Alzheimers disease
Animals
Base Sequence
Biological and medical sciences
brain
Brain - metabolism
Clusterin
Cricetinae
DNA
Fundamental and applied biological sciences. Psychology
Gene expression
Genes
Glial Fibrillary Acidic Protein - genetics
glycoproteins
Glycoproteins - genetics
Libraries
Messenger RNA
Metallothionein - genetics
Molecular and cellular biology
Molecular Chaperones
Molecular genetics
Molecular Sequence Data
Nerve Tissue Proteins - genetics
Nervous system diseases
Neurodegenerative diseases
Nucleic acids
Rats
RNA
RNA, Messenger - genetics
Scrapie - genetics
Scrapie - metabolism
Sequence Homology, Nucleic Acid
Transcription, Genetic
transferrin
Transferrin - genetics
Transferrins
title Changes in Brain Gene Expression Shared by Scrapie and Alzheimer Disease
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