Gene structure, localization and role in oxidative stress of methionine sulfoxide reductase A (MSRA) in the monkey retina
MSRA (EC 1.8.4.6) is a member of the methionine sulfoxide reductase family that can reduce methionine sulfoxide (MetO) in proteins. This repair function has been shown to protect cells against oxidative damage. In this study we have assembled the complete gene structure of msrA and identified the pr...
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| Published in | Experimental eye research Vol. 82; no. 5; pp. 816 - 827 |
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| Main Authors | , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
England
Elsevier Ltd
01.05.2006
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| Subjects | |
| Online Access | Get full text |
| ISSN | 0014-4835 1096-0007 1096-0007 |
| DOI | 10.1016/j.exer.2005.10.003 |
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| Abstract | MSRA (EC 1.8.4.6) is a member of the methionine sulfoxide reductase family that can reduce methionine sulfoxide (MetO) in proteins. This repair function has been shown to protect cells against oxidative damage. In this study we have assembled the complete gene structure of msrA and identified the presence of two distinct putative promoters that generate three different transcripts. These transcripts were cloned by 5'RACE and code for three MSRA isoforms with different N-termini. The different forms of MSRA target to distinct intracellular regions. The main MSRA transcript (msrA1) had been previously shown to target the mitochondria. MsrA2 and 3 originate from a second promoter and target the cytosol and nuclei. In the monkey retina msrA message was detected mainly in the macular RPE-choroid region while its activity was measured mainly in the soluble fractions of fractionated neural retina and RPE-choroid. The MSRA protein is found throughout the retina but is especially abundant at the photoreceptor synapses, ganglion and Müller cells. Interestingly, MSRA was not detected in the mitochondria of the photoreceptor inner segments. The RPE in the peripheral retina shows very low levels of expression but the RPE in the macular region is strongly labeled. Targeted silencing of msrA message rendered cultured RPE cells more sensitive to oxidative damage suggesting a role for MSRA in RPE protection against oxidative stress. Collectively these data suggest MSRA may play an important role in protecting macular RPE from oxidative damage. |
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| AbstractList | MSRA (EC 1.8.4.6) is a member of the methionine sulfoxide reductase family that can reduce methionine sulfoxide (MetO) in proteins. This repair function has been shown to protect cells against oxidative damage. In this study we have assembled the complete gene structure of msrA and identified the presence of two distinct putative promoters that generate three different transcripts. These transcripts were cloned by 5'RACE and code for three MSRA isoforms with different N-termini. The different forms of MSRA target to distinct intracellular regions. The main MSRA transcript (msrA1) had been previously shown to target the mitochondria. MsrA2 and 3 originate from a second promoter and target the cytosol and nuclei. In the monkey retina msrA message was detected mainly in the macular RPE-choroid region while its activity was measured mainly in the soluble fractions of fractionated neural retina and RPE-choroid. The MSRA protein is found throughout the retina but is especially abundant at the photoreceptor synapses, ganglion and Müller cells. Interestingly, MSRA was not detected in the mitochondria of the photoreceptor inner segments. The RPE in the peripheral retina shows very low levels of expression but the RPE in the macular region is strongly labeled. Targeted silencing of msrA message rendered cultured RPE cells more sensitive to oxidative damage suggesting a role for MSRA in RPE protection against oxidative stress. Collectively these data suggest MSRA may play an important role in protecting macular RPE from oxidative damage. MSRA (EC 1.8.4.6) is a member of the methionine sulfoxide reductase family that can reduce methionine sulfoxide (MetO) in proteins. This repair function has been shown to protect cells against oxidative damage. In this study we have assembled the complete gene structure of msrA and identified the presence of two distinct putative promoters that generate three different transcripts. These transcripts were cloned by 5'RACE and code for three MSRA isoforms with different N-termini. The different forms of MSRA target to distinct intracellular regions. The main MSRA transcript (msrA1) had been previously shown to target the mitochondria. MsrA2 and 3 originate from a second promoter and target the cytosol and nuclei. In the monkey retina msrA message was detected mainly in the macular RPE-choroid region while its activity was measured mainly in the soluble fractions of fractionated neural retina and RPE-choroid. The MSRA protein is found throughout the retina but is especially abundant at the photoreceptor synapses, ganglion and Müller cells. Interestingly, MSRA was not detected in the mitochondria of the photoreceptor inner segments. The RPE in the peripheral retina shows very low levels of expression but the RPE in the macular region is strongly labeled. Targeted silencing of msrA message rendered cultured RPE cells more sensitive to oxidative damage suggesting a role for MSRA in RPE protection against oxidative stress. Collectively these data suggest MSRA may play an important role in protecting macular RPE from oxidative damage.MSRA (EC 1.8.4.6) is a member of the methionine sulfoxide reductase family that can reduce methionine sulfoxide (MetO) in proteins. This repair function has been shown to protect cells against oxidative damage. In this study we have assembled the complete gene structure of msrA and identified the presence of two distinct putative promoters that generate three different transcripts. These transcripts were cloned by 5'RACE and code for three MSRA isoforms with different N-termini. The different forms of MSRA target to distinct intracellular regions. The main MSRA transcript (msrA1) had been previously shown to target the mitochondria. MsrA2 and 3 originate from a second promoter and target the cytosol and nuclei. In the monkey retina msrA message was detected mainly in the macular RPE-choroid region while its activity was measured mainly in the soluble fractions of fractionated neural retina and RPE-choroid. The MSRA protein is found throughout the retina but is especially abundant at the photoreceptor synapses, ganglion and Müller cells. Interestingly, MSRA was not detected in the mitochondria of the photoreceptor inner segments. The RPE in the peripheral retina shows very low levels of expression but the RPE in the macular region is strongly labeled. Targeted silencing of msrA message rendered cultured RPE cells more sensitive to oxidative damage suggesting a role for MSRA in RPE protection against oxidative stress. Collectively these data suggest MSRA may play an important role in protecting macular RPE from oxidative damage. |
| Author | Rodriguez, I.R. Alam, S. Kantorow, M. Marchetti, M. Sagher, D. Tserentsoodol, N. Weissbach, H. Lee, J.W. Gordiyenko, N.V. |
| AuthorAffiliation | c Center for Molecular Biology and Biotechnology, Florida Atlantic University, Boca Raton, FL 33437, USA a Lab of Retinal Cell and Molecular Biology, Mechanisms of Retinal Diseases Section, National Eye Institute, NIH, 7 Memorial drive MSC 0706, Bethesda, MD 20892, USA b Department of Biomedical Science, Florida Atlantic University, Boca Raton, FL 33437, USA |
| AuthorAffiliation_xml | – name: b Department of Biomedical Science, Florida Atlantic University, Boca Raton, FL 33437, USA – name: c Center for Molecular Biology and Biotechnology, Florida Atlantic University, Boca Raton, FL 33437, USA – name: a Lab of Retinal Cell and Molecular Biology, Mechanisms of Retinal Diseases Section, National Eye Institute, NIH, 7 Memorial drive MSC 0706, Bethesda, MD 20892, USA |
| Author_xml | – sequence: 1 givenname: J.W. surname: Lee fullname: Lee, J.W. organization: Lab of Retinal Cell and Molecular Biology, Mechanisms of Retinal Diseases Section, National Eye Institute, NIH, 7 Memorial drive MSC 0706, Bethesda, MD 20892, USA – sequence: 2 givenname: N.V. surname: Gordiyenko fullname: Gordiyenko, N.V. organization: Lab of Retinal Cell and Molecular Biology, Mechanisms of Retinal Diseases Section, National Eye Institute, NIH, 7 Memorial drive MSC 0706, Bethesda, MD 20892, USA – sequence: 3 givenname: M. surname: Marchetti fullname: Marchetti, M. organization: Department of Biomedical Science, Florida Atlantic University, Boca Raton, FL 33437, USA – sequence: 4 givenname: N. surname: Tserentsoodol fullname: Tserentsoodol, N. organization: Lab of Retinal Cell and Molecular Biology, Mechanisms of Retinal Diseases Section, National Eye Institute, NIH, 7 Memorial drive MSC 0706, Bethesda, MD 20892, USA – sequence: 5 givenname: D. surname: Sagher fullname: Sagher, D. organization: Center for Molecular Biology and Biotechnology, Florida Atlantic University, Boca Raton, FL 33437, USA – sequence: 6 givenname: S. surname: Alam fullname: Alam, S. organization: Lab of Retinal Cell and Molecular Biology, Mechanisms of Retinal Diseases Section, National Eye Institute, NIH, 7 Memorial drive MSC 0706, Bethesda, MD 20892, USA – sequence: 7 givenname: H. surname: Weissbach fullname: Weissbach, H. organization: Center for Molecular Biology and Biotechnology, Florida Atlantic University, Boca Raton, FL 33437, USA – sequence: 8 givenname: M. surname: Kantorow fullname: Kantorow, M. organization: Department of Biomedical Science, Florida Atlantic University, Boca Raton, FL 33437, USA – sequence: 9 givenname: I.R. surname: Rodriguez fullname: Rodriguez, I.R. email: rodriguezi@nei.nih.gov organization: Lab of Retinal Cell and Molecular Biology, Mechanisms of Retinal Diseases Section, National Eye Institute, NIH, 7 Memorial drive MSC 0706, Bethesda, MD 20892, USA |
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| Keywords | gene structure MPC PPC methionine sulfoxide reductase IPL CH mitochondria RPE INL OPL ONL MNR GCL MSRA TBHP retina PNR ROS RIS macula 5'RACE |
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| SubjectTerms | Amino Acid Sequence Animals Cell Death Gene Expression Gene Silencing gene structure Humans Macaca mulatta - metabolism macula Macula Lutea - enzymology methionine sulfoxide reductase Methionine Sulfoxide Reductases mitochondria Molecular Sequence Data Open Reading Frames - genetics Oxidative Stress - physiology Oxidoreductases - genetics Oxidoreductases - metabolism Oxidoreductases - physiology retina Retina - enzymology Reverse Transcriptase Polymerase Chain Reaction - methods RNA, Messenger - genetics Sequence Alignment Transcription, Genetic |
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| Title | Gene structure, localization and role in oxidative stress of methionine sulfoxide reductase A (MSRA) in the monkey retina |
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