The biological foundation of the genetic association of TOMM40 with late-onset Alzheimer's disease
A variable-length poly-T variant in intron 6 of the TOMM40 gene, rs10524523, is associated with risk and age-of-onset of sporadic (late-onset) Alzheimer's disease. In Caucasians, the three predominant alleles at this locus are Short (S), Long (L) or Very long (VL). On an APOE ε3/3 background, t...
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description | A variable-length poly-T variant in intron 6 of the TOMM40 gene, rs10524523, is associated with risk and age-of-onset of sporadic (late-onset) Alzheimer's disease. In Caucasians, the three predominant alleles at this locus are Short (S), Long (L) or Very long (VL). On an APOE ε3/3 background, the S/VL and VL/VL genotypes are more protective than S/S. The '523 poly-T has regulatory properties, in that the VL poly-T results in higher expression than the S poly-T in luciferase expression systems. The aim of the current work was to identify effects on cellular bioenergetics of increased TOM40 protein expression. MitoTracker Green fluorescence and autophagic vesicle staining was the same in control and over-expressing cells, but TOM40 over-expression was associated with increased expression of TOM20, a preprotein receptor of the TOM complex, the mitochondrial chaperone HSPA9, and PDHE1a, and increased activities of the oxidative phosphorylation complexes I and IV and of the TCA member α-ketoglutaric acid dehydrogenase. Consistent with the complex I findings, respiration was more sensitive to inhibition by rotenone in control cells than in the TOM40 over-expressing cells. In the absence of inhibitors, total cellular ATP, the mitochondrial membrane potential, and respiration were elevated in the over-expressing cells. Spare respiratory capacity was greater in the TOM40 over-expressing cells than in the controls. TOM40 over-expression blocked Ab-elicited decreases in the mitochondrial membrane potential, cellular ATP levels, and cellular viability in the control cells. These data suggest elevated expression of TOM40 may be protective of mitochondrial function.
•An intronic poly-T in TOMM40, rs10524523, is linked to age-of-onset of sporadic Alzheimer's disease.•The allele lengths are Short (S), Long (L) or Very long (VL).•In APOE e3/e3 homogygotes, L/VL genotypes are more protective than S/S.•The VL poly-T results in higher expression than the S poly-T in luciferase expression systems.•Over-expression of TOM40 in HeLa cells enhances mitochondrial efficiency.•Tom40 over-expression is protective against beta-amyloid-induced cellular damage |
doi_str_mv | 10.1016/j.bbadis.2017.07.031 |
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•An intronic poly-T in TOMM40, rs10524523, is linked to age-of-onset of sporadic Alzheimer's disease.•The allele lengths are Short (S), Long (L) or Very long (VL).•In APOE e3/e3 homogygotes, L/VL genotypes are more protective than S/S.•The VL poly-T results in higher expression than the S poly-T in luciferase expression systems.•Over-expression of TOM40 in HeLa cells enhances mitochondrial efficiency.•Tom40 over-expression is protective against beta-amyloid-induced cellular damage</description><identifier>ISSN: 0925-4439</identifier><identifier>ISSN: 0006-3002</identifier><identifier>EISSN: 1879-260X</identifier><identifier>EISSN: 1878-2434</identifier><identifier>DOI: 10.1016/j.bbadis.2017.07.031</identifier><identifier>PMID: 28768149</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Alzheimer Disease - genetics ; Alzheimer Disease - metabolism ; Alzheimer Disease - pathology ; Alzheimer's ; Apolipoproteins E - genetics ; Apolipoproteins E - metabolism ; Electron Transport Complex I - genetics ; Electron Transport Complex I - metabolism ; Energetics ; Female ; Gene Expression Regulation ; Genetic Loci ; HeLa Cells ; HSP70 Heat-Shock Proteins - genetics ; HSP70 Heat-Shock Proteins - metabolism ; Humans ; Ketoglutarate Dehydrogenase Complex - genetics ; Ketoglutarate Dehydrogenase Complex - metabolism ; Membrane Potential, Mitochondrial - genetics ; Membrane Transport Proteins - biosynthesis ; Membrane Transport Proteins - genetics ; Mitochondria ; Mitochondria - genetics ; Mitochondria - metabolism ; Mitochondria - pathology ; Mitochondrial Proteins - genetics ; Mitochondrial Proteins - metabolism ; Neurodegeneration ; Receptors, Cell Surface - biosynthesis ; Receptors, Cell Surface - genetics ; TOM ; TOMM40</subject><ispartof>Biochimica et biophysica acta, 2017-11, Vol.1863 (11), p.2973-2986</ispartof><rights>2017 The Authors</rights><rights>Copyright © 2017 The Authors. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-58b6b31b11d98abce1e8deef65641a5d4ac71f9f6a3fe552c7336f7a60f79a113</citedby><cites>FETCH-LOGICAL-c463t-58b6b31b11d98abce1e8deef65641a5d4ac71f9f6a3fe552c7336f7a60f79a113</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.bbadis.2017.07.031$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28768149$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zeitlow, Kahli</creatorcontrib><creatorcontrib>Charlambous, Lefko</creatorcontrib><creatorcontrib>Ng, Isaac</creatorcontrib><creatorcontrib>Gagrani, Sonal</creatorcontrib><creatorcontrib>Mihovilovic, Mirta</creatorcontrib><creatorcontrib>Luo, Shuhong</creatorcontrib><creatorcontrib>Rock, Daniel L.</creatorcontrib><creatorcontrib>Saunders, Ann</creatorcontrib><creatorcontrib>Roses, Allen D.</creatorcontrib><creatorcontrib>Gottschalk, W. Kirby</creatorcontrib><title>The biological foundation of the genetic association of TOMM40 with late-onset Alzheimer's disease</title><title>Biochimica et biophysica acta</title><addtitle>Biochim Biophys Acta Mol Basis Dis</addtitle><description>A variable-length poly-T variant in intron 6 of the TOMM40 gene, rs10524523, is associated with risk and age-of-onset of sporadic (late-onset) Alzheimer's disease. In Caucasians, the three predominant alleles at this locus are Short (S), Long (L) or Very long (VL). On an APOE ε3/3 background, the S/VL and VL/VL genotypes are more protective than S/S. The '523 poly-T has regulatory properties, in that the VL poly-T results in higher expression than the S poly-T in luciferase expression systems. The aim of the current work was to identify effects on cellular bioenergetics of increased TOM40 protein expression. MitoTracker Green fluorescence and autophagic vesicle staining was the same in control and over-expressing cells, but TOM40 over-expression was associated with increased expression of TOM20, a preprotein receptor of the TOM complex, the mitochondrial chaperone HSPA9, and PDHE1a, and increased activities of the oxidative phosphorylation complexes I and IV and of the TCA member α-ketoglutaric acid dehydrogenase. Consistent with the complex I findings, respiration was more sensitive to inhibition by rotenone in control cells than in the TOM40 over-expressing cells. In the absence of inhibitors, total cellular ATP, the mitochondrial membrane potential, and respiration were elevated in the over-expressing cells. Spare respiratory capacity was greater in the TOM40 over-expressing cells than in the controls. TOM40 over-expression blocked Ab-elicited decreases in the mitochondrial membrane potential, cellular ATP levels, and cellular viability in the control cells. These data suggest elevated expression of TOM40 may be protective of mitochondrial function.
•An intronic poly-T in TOMM40, rs10524523, is linked to age-of-onset of sporadic Alzheimer's disease.•The allele lengths are Short (S), Long (L) or Very long (VL).•In APOE e3/e3 homogygotes, L/VL genotypes are more protective than S/S.•The VL poly-T results in higher expression than the S poly-T in luciferase expression systems.•Over-expression of TOM40 in HeLa cells enhances mitochondrial efficiency.•Tom40 over-expression is protective against beta-amyloid-induced cellular damage</description><subject>Alzheimer Disease - genetics</subject><subject>Alzheimer Disease - metabolism</subject><subject>Alzheimer Disease - pathology</subject><subject>Alzheimer's</subject><subject>Apolipoproteins E - genetics</subject><subject>Apolipoproteins E - metabolism</subject><subject>Electron Transport Complex I - genetics</subject><subject>Electron Transport Complex I - metabolism</subject><subject>Energetics</subject><subject>Female</subject><subject>Gene Expression Regulation</subject><subject>Genetic Loci</subject><subject>HeLa Cells</subject><subject>HSP70 Heat-Shock Proteins - genetics</subject><subject>HSP70 Heat-Shock Proteins - metabolism</subject><subject>Humans</subject><subject>Ketoglutarate Dehydrogenase Complex - genetics</subject><subject>Ketoglutarate Dehydrogenase Complex - metabolism</subject><subject>Membrane Potential, Mitochondrial - genetics</subject><subject>Membrane Transport Proteins - biosynthesis</subject><subject>Membrane Transport Proteins - genetics</subject><subject>Mitochondria</subject><subject>Mitochondria - genetics</subject><subject>Mitochondria - metabolism</subject><subject>Mitochondria - pathology</subject><subject>Mitochondrial Proteins - genetics</subject><subject>Mitochondrial Proteins - metabolism</subject><subject>Neurodegeneration</subject><subject>Receptors, Cell Surface - biosynthesis</subject><subject>Receptors, Cell Surface - genetics</subject><subject>TOM</subject><subject>TOMM40</subject><issn>0925-4439</issn><issn>0006-3002</issn><issn>1879-260X</issn><issn>1878-2434</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UU1vEzEQtRCIhsI_QMg3uGzwrHft9QWpqviSWvUSJG6W7R0njjbrYjtF9NfXUUqAC6OR5vBm3ryZR8hrYEtgIN5vl9aaMeRly0AuWU0OT8gCBqmaVrDvT8mCqbZvuo6rM_Ii5y2rISR7Ts7aQYoBOrUgdrVBakOc4jo4M1Ef9_NoSogzjZ6WCq5xxhIcNTlHF07Q6ub6umP0ZygbOpmCTZwzFnox3W8w7DC9zbSKQ5PxJXnmzZTx1WM9J98-fVxdfmmubj5_vby4alwneGn6wQrLwQKMajDWIeAwInrRiw5MP3bGSfDKC8M99n3rJOfCSyOYl8oA8HPy4ch7u7c7HB3OJZlJ36awM-mXjibof5E5bPQ63ule9GpQshK8eyRI8ccec9G7kB1Ok5kx7rOG-s5BcSVEbe2OrS7FnBP60xpg-mCP3uqjPfpgj2Y1-UHim78lnoZ--_HnBqyPuguYdHYBZ4djSOiKHmP4_4YHUcalDQ</recordid><startdate>20171101</startdate><enddate>20171101</enddate><creator>Zeitlow, Kahli</creator><creator>Charlambous, Lefko</creator><creator>Ng, Isaac</creator><creator>Gagrani, Sonal</creator><creator>Mihovilovic, Mirta</creator><creator>Luo, Shuhong</creator><creator>Rock, Daniel L.</creator><creator>Saunders, Ann</creator><creator>Roses, Allen D.</creator><creator>Gottschalk, W. Kirby</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20171101</creationdate><title>The biological foundation of the genetic association of TOMM40 with late-onset Alzheimer's disease</title><author>Zeitlow, Kahli ; Charlambous, Lefko ; Ng, Isaac ; Gagrani, Sonal ; Mihovilovic, Mirta ; Luo, Shuhong ; Rock, Daniel L. ; Saunders, Ann ; Roses, Allen D. ; Gottschalk, W. Kirby</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-58b6b31b11d98abce1e8deef65641a5d4ac71f9f6a3fe552c7336f7a60f79a113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Alzheimer Disease - genetics</topic><topic>Alzheimer Disease - metabolism</topic><topic>Alzheimer Disease - pathology</topic><topic>Alzheimer's</topic><topic>Apolipoproteins E - genetics</topic><topic>Apolipoproteins E - metabolism</topic><topic>Electron Transport Complex I - genetics</topic><topic>Electron Transport Complex I - metabolism</topic><topic>Energetics</topic><topic>Female</topic><topic>Gene Expression Regulation</topic><topic>Genetic Loci</topic><topic>HeLa Cells</topic><topic>HSP70 Heat-Shock Proteins - genetics</topic><topic>HSP70 Heat-Shock Proteins - metabolism</topic><topic>Humans</topic><topic>Ketoglutarate Dehydrogenase Complex - genetics</topic><topic>Ketoglutarate Dehydrogenase Complex - metabolism</topic><topic>Membrane Potential, Mitochondrial - genetics</topic><topic>Membrane Transport Proteins - biosynthesis</topic><topic>Membrane Transport Proteins - genetics</topic><topic>Mitochondria</topic><topic>Mitochondria - genetics</topic><topic>Mitochondria - metabolism</topic><topic>Mitochondria - pathology</topic><topic>Mitochondrial Proteins - genetics</topic><topic>Mitochondrial Proteins - metabolism</topic><topic>Neurodegeneration</topic><topic>Receptors, Cell Surface - biosynthesis</topic><topic>Receptors, Cell Surface - genetics</topic><topic>TOM</topic><topic>TOMM40</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zeitlow, Kahli</creatorcontrib><creatorcontrib>Charlambous, Lefko</creatorcontrib><creatorcontrib>Ng, Isaac</creatorcontrib><creatorcontrib>Gagrani, Sonal</creatorcontrib><creatorcontrib>Mihovilovic, Mirta</creatorcontrib><creatorcontrib>Luo, Shuhong</creatorcontrib><creatorcontrib>Rock, Daniel L.</creatorcontrib><creatorcontrib>Saunders, Ann</creatorcontrib><creatorcontrib>Roses, Allen D.</creatorcontrib><creatorcontrib>Gottschalk, W. Kirby</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biochimica et biophysica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zeitlow, Kahli</au><au>Charlambous, Lefko</au><au>Ng, Isaac</au><au>Gagrani, Sonal</au><au>Mihovilovic, Mirta</au><au>Luo, Shuhong</au><au>Rock, Daniel L.</au><au>Saunders, Ann</au><au>Roses, Allen D.</au><au>Gottschalk, W. Kirby</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The biological foundation of the genetic association of TOMM40 with late-onset Alzheimer's disease</atitle><jtitle>Biochimica et biophysica acta</jtitle><addtitle>Biochim Biophys Acta Mol Basis Dis</addtitle><date>2017-11-01</date><risdate>2017</risdate><volume>1863</volume><issue>11</issue><spage>2973</spage><epage>2986</epage><pages>2973-2986</pages><issn>0925-4439</issn><issn>0006-3002</issn><eissn>1879-260X</eissn><eissn>1878-2434</eissn><abstract>A variable-length poly-T variant in intron 6 of the TOMM40 gene, rs10524523, is associated with risk and age-of-onset of sporadic (late-onset) Alzheimer's disease. In Caucasians, the three predominant alleles at this locus are Short (S), Long (L) or Very long (VL). On an APOE ε3/3 background, the S/VL and VL/VL genotypes are more protective than S/S. The '523 poly-T has regulatory properties, in that the VL poly-T results in higher expression than the S poly-T in luciferase expression systems. The aim of the current work was to identify effects on cellular bioenergetics of increased TOM40 protein expression. MitoTracker Green fluorescence and autophagic vesicle staining was the same in control and over-expressing cells, but TOM40 over-expression was associated with increased expression of TOM20, a preprotein receptor of the TOM complex, the mitochondrial chaperone HSPA9, and PDHE1a, and increased activities of the oxidative phosphorylation complexes I and IV and of the TCA member α-ketoglutaric acid dehydrogenase. Consistent with the complex I findings, respiration was more sensitive to inhibition by rotenone in control cells than in the TOM40 over-expressing cells. In the absence of inhibitors, total cellular ATP, the mitochondrial membrane potential, and respiration were elevated in the over-expressing cells. Spare respiratory capacity was greater in the TOM40 over-expressing cells than in the controls. TOM40 over-expression blocked Ab-elicited decreases in the mitochondrial membrane potential, cellular ATP levels, and cellular viability in the control cells. These data suggest elevated expression of TOM40 may be protective of mitochondrial function.
•An intronic poly-T in TOMM40, rs10524523, is linked to age-of-onset of sporadic Alzheimer's disease.•The allele lengths are Short (S), Long (L) or Very long (VL).•In APOE e3/e3 homogygotes, L/VL genotypes are more protective than S/S.•The VL poly-T results in higher expression than the S poly-T in luciferase expression systems.•Over-expression of TOM40 in HeLa cells enhances mitochondrial efficiency.•Tom40 over-expression is protective against beta-amyloid-induced cellular damage</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>28768149</pmid><doi>10.1016/j.bbadis.2017.07.031</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alzheimer Disease - genetics Alzheimer Disease - metabolism Alzheimer Disease - pathology Alzheimer's Apolipoproteins E - genetics Apolipoproteins E - metabolism Electron Transport Complex I - genetics Electron Transport Complex I - metabolism Energetics Female Gene Expression Regulation Genetic Loci HeLa Cells HSP70 Heat-Shock Proteins - genetics HSP70 Heat-Shock Proteins - metabolism Humans Ketoglutarate Dehydrogenase Complex - genetics Ketoglutarate Dehydrogenase Complex - metabolism Membrane Potential, Mitochondrial - genetics Membrane Transport Proteins - biosynthesis Membrane Transport Proteins - genetics Mitochondria Mitochondria - genetics Mitochondria - metabolism Mitochondria - pathology Mitochondrial Proteins - genetics Mitochondrial Proteins - metabolism Neurodegeneration Receptors, Cell Surface - biosynthesis Receptors, Cell Surface - genetics TOM TOMM40 |
title | The biological foundation of the genetic association of TOMM40 with late-onset Alzheimer's disease |
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