Gene Expression of CRAL_TRIO Family Proteins modulated by Vitamin E Deficiency in Zebrafish (Danio Rerio)

•Alpha-tocopherol transfer protein (α-TTP) is a highly conserved protein•α-TTP is a member of CRAL_TRIO, a lipid binding protein family•Vitamin E deficiency causes lipid peroxidation•Gene expression responses show impacts to phospholipid and choline metabolism An evaluation of the impact of vitamin...

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Veröffentlicht in:The Journal of nutritional biochemistry 2021-11, Vol.97, p.108801-108801, Article 108801
Hauptverfasser: Watt, Alexander T., Head, Brian, Leonard, Scott W., Tanguay, Robyn L., Traber, Maret G.
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container_title The Journal of nutritional biochemistry
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creator Watt, Alexander T.
Head, Brian
Leonard, Scott W.
Tanguay, Robyn L.
Traber, Maret G.
description •Alpha-tocopherol transfer protein (α-TTP) is a highly conserved protein•α-TTP is a member of CRAL_TRIO, a lipid binding protein family•Vitamin E deficiency causes lipid peroxidation•Gene expression responses show impacts to phospholipid and choline metabolism An evaluation of the impact of vitamin E deficiency on expression of the alpha-tocopherol transfer protein (α-TTP) and related CRAL_TRIO genes was undertaken using livers from adult zebrafish based on the hypothesis that increased lipid peroxidation would modulate gene expression. Zebrafish were fed either a vitamin E sufficient (E+) or deficient (E–) diet for 9 months, then fish were euthanized, and livers were harvested. Livers from the E+ relative to E– fish contained 40-times more α-tocopherol (P
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Zebrafish were fed either a vitamin E sufficient (E+) or deficient (E–) diet for 9 months, then fish were euthanized, and livers were harvested. Livers from the E+ relative to E– fish contained 40-times more α-tocopherol (P &lt;0.0001) and one fourth the malondialdehyde (P = 0.0153). RNA was extracted from E+ and E– livers, then subject to evaluation of gene expression of ttpa and other genes of the CRAL_TRIO family, genes of antioxidant markers, and genes related to lipid metabolism. Ttpa expression was not altered by vitamin E status. However, one member of the CRAL_TRIO family, tyrosine-protein phosphatase non-receptor type 9 gene (ptpn9a), showed a 2.4-fold increase (P = 0.029) in E– relative to E+ livers. Further, we identified that the gene for choline kinase alpha (chka) showed a 3.0-fold increase (P = 0.010) in E– livers. These outcomes are consistent with our previous findings that show vitamin E deficiency increased lipid peroxidation causing increases in phospholipid turnover. 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Zebrafish were fed either a vitamin E sufficient (E+) or deficient (E–) diet for 9 months, then fish were euthanized, and livers were harvested. Livers from the E+ relative to E– fish contained 40-times more α-tocopherol (P &lt;0.0001) and one fourth the malondialdehyde (P = 0.0153). RNA was extracted from E+ and E– livers, then subject to evaluation of gene expression of ttpa and other genes of the CRAL_TRIO family, genes of antioxidant markers, and genes related to lipid metabolism. Ttpa expression was not altered by vitamin E status. However, one member of the CRAL_TRIO family, tyrosine-protein phosphatase non-receptor type 9 gene (ptpn9a), showed a 2.4-fold increase (P = 0.029) in E– relative to E+ livers. Further, we identified that the gene for choline kinase alpha (chka) showed a 3.0-fold increase (P = 0.010) in E– livers. These outcomes are consistent with our previous findings that show vitamin E deficiency increased lipid peroxidation causing increases in phospholipid turnover. [Display omitted]</description><subject>alpha-Tocopherol - metabolism</subject><subject>Alpha-tocopherol transfer protein (α-TTP)</subject><subject>Animals</subject><subject>Antioxidants</subject><subject>Carrier Proteins - genetics</subject><subject>Carrier Proteins - metabolism</subject><subject>Choline</subject><subject>Choline Kinase - genetics</subject><subject>Choline Kinase - metabolism</subject><subject>CRAL_TRIO</subject><subject>Gene Expression</subject><subject>Lipid Metabolism - genetics</subject><subject>Liver - metabolism</subject><subject>Malondialdehyde - metabolism</subject><subject>Protein Tyrosine Phosphatases, Non-Receptor - genetics</subject><subject>Protein Tyrosine Phosphatases, Non-Receptor - metabolism</subject><subject>Ptpn9a</subject><subject>SEC14</subject><subject>Vitamin E Deficiency - genetics</subject><subject>Vitamin E Deficiency - metabolism</subject><subject>Zebrafish</subject><subject>Zebrafish Proteins - genetics</subject><subject>Zebrafish Proteins - metabolism</subject><issn>0955-2863</issn><issn>1873-4847</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1vEzEQhi0EoqHwE0A-0sMGe_2xzglVaVoqRSqKCgcultce04kSO7I3Ffn3bEkpcOI0mo_3nZmHkLecTTnj-sN6uk77occ8bVnLx5oxjD8jE2460Ugju-dkwmZKNa3R4oS8qnXNGGul0i_JiZCcz7RgE4JXkIAufuwK1Io50RzpfHW-tLer6xt66ba4OdDPJQ-AqdJtDvuNGyDQ_kC_4jC2E13QC4joEZI_0DH_Bn1xEesdfX_hEma6goL57DV5Ed2mwpvHeEq-XC5u55-a5c3V9fx82XipzdBwoTjTTEIbGUAMvfJcqi6GTnfMzAxT41PSSaek70wXdeDGtwJ8kLI3QopT8vHou9v3Wwge0lDcxu4Kbl052OzQ_ttJeGe_53s7Ym1nTHSjgzo6-JJrLRCfxJw9TGm7to_w7QN8e4Q_6t79vflJ9Zv2n9Ng_P8eodj6CxsELOAHGzL-Z8VPsvaYnA</recordid><startdate>20211101</startdate><enddate>20211101</enddate><creator>Watt, Alexander T.</creator><creator>Head, Brian</creator><creator>Leonard, Scott W.</creator><creator>Tanguay, Robyn L.</creator><creator>Traber, Maret G.</creator><general>Elsevier Inc</general><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>5PM</scope><orcidid>https://orcid.org/0000-0002-7520-2227</orcidid><orcidid>https://orcid.org/0000-0002-2892-4024</orcidid></search><sort><creationdate>20211101</creationdate><title>Gene Expression of CRAL_TRIO Family Proteins modulated by Vitamin E Deficiency in Zebrafish (Danio Rerio)</title><author>Watt, Alexander T. ; 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Zebrafish were fed either a vitamin E sufficient (E+) or deficient (E–) diet for 9 months, then fish were euthanized, and livers were harvested. Livers from the E+ relative to E– fish contained 40-times more α-tocopherol (P &lt;0.0001) and one fourth the malondialdehyde (P = 0.0153). RNA was extracted from E+ and E– livers, then subject to evaluation of gene expression of ttpa and other genes of the CRAL_TRIO family, genes of antioxidant markers, and genes related to lipid metabolism. Ttpa expression was not altered by vitamin E status. However, one member of the CRAL_TRIO family, tyrosine-protein phosphatase non-receptor type 9 gene (ptpn9a), showed a 2.4-fold increase (P = 0.029) in E– relative to E+ livers. Further, we identified that the gene for choline kinase alpha (chka) showed a 3.0-fold increase (P = 0.010) in E– livers. These outcomes are consistent with our previous findings that show vitamin E deficiency increased lipid peroxidation causing increases in phospholipid turnover. [Display omitted]</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>34119630</pmid><doi>10.1016/j.jnutbio.2021.108801</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-7520-2227</orcidid><orcidid>https://orcid.org/0000-0002-2892-4024</orcidid><oa>free_for_read</oa></addata></record>
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subjects alpha-Tocopherol - metabolism
Alpha-tocopherol transfer protein (α-TTP)
Animals
Antioxidants
Carrier Proteins - genetics
Carrier Proteins - metabolism
Choline
Choline Kinase - genetics
Choline Kinase - metabolism
CRAL_TRIO
Gene Expression
Lipid Metabolism - genetics
Liver - metabolism
Malondialdehyde - metabolism
Protein Tyrosine Phosphatases, Non-Receptor - genetics
Protein Tyrosine Phosphatases, Non-Receptor - metabolism
Ptpn9a
SEC14
Vitamin E Deficiency - genetics
Vitamin E Deficiency - metabolism
Zebrafish
Zebrafish Proteins - genetics
Zebrafish Proteins - metabolism
title Gene Expression of CRAL_TRIO Family Proteins modulated by Vitamin E Deficiency in Zebrafish (Danio Rerio)
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