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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Veröffentlicht in:Biochimica et biophysica acta 2017-11, Vol.1863 (11), p.2973-2986
Hauptverfasser: Zeitlow, Kahli, Charlambous, Lefko, Ng, Isaac, Gagrani, Sonal, Mihovilovic, Mirta, Luo, Shuhong, Rock, Daniel L., Saunders, Ann, Roses, Allen D., Gottschalk, W. Kirby
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container_issue 11
container_start_page 2973
container_title Biochimica et biophysica acta
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creator Zeitlow, Kahli
Charlambous, Lefko
Ng, Isaac
Gagrani, Sonal
Mihovilovic, Mirta
Luo, Shuhong
Rock, Daniel L.
Saunders, Ann
Roses, Allen D.
Gottschalk, W. Kirby
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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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. 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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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