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Molecular genetic and biochemical characterization of a putative family of zinc metalloproteins in Caenorhabditis elegans
Four highly similar genes (W08E12.2, W08E12.3, W08E12.4 and W08E12.5) which are consecutively aligned on chromosome IV of the C. elegans genome are predicted to code for small (120–141aa) yet cysteine rich (18–19 cysteines) proteins. Cloning and sequencing of the genomic regions of the isoforms conf...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336089/ https://www.ncbi.nlm.nih.gov/pubmed/30444224 http://dx.doi.org/10.1039/c8mt00169c |
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author | Chaudhuri, Poulami Imam, Hasan Tanvir Essig, Yona Krasauskas, Jovaras Webb, Samuel M. Blindauer, Claudia A. Stürzenbaum, Stephen R. |
author_facet | Chaudhuri, Poulami Imam, Hasan Tanvir Essig, Yona Krasauskas, Jovaras Webb, Samuel M. Blindauer, Claudia A. Stürzenbaum, Stephen R. |
author_sort | Chaudhuri, Poulami |
collection | PubMed |
description | Four highly similar genes (W08E12.2, W08E12.3, W08E12.4 and W08E12.5) which are consecutively aligned on chromosome IV of the C. elegans genome are predicted to code for small (120–141aa) yet cysteine rich (18–19 cysteines) proteins. Cloning and sequencing of the genomic regions of the isoforms confirmed the presence and order of all genes. The generation of transgenic worms strains with an integrated single copy or extrachromosomal multi-copy PW08E12.3;W08E12.4::GFP uncovered that W08E12.3 and W08E12.4 are constitutively expressed in the pharynx and significantly induced in worms exposed to 100 μM Zn. Knockdown by RNAi did not have a marked consequence on reproductive performance nor was a Zn-dependent effect on nematode growth observed. However, RNAi of these genes led to an accumulation of Zn in the intestinal cells. W08E12.3 was recombinantly expressed in E. coli and the purified protein was shown to be able to bind up to 6.5 Zn molecules at neutral pH. Zn-binding was acid-labile and the apo protein was observed at pH < 4.3. This characterization suggests W08E12.2, W08E12.3, W08E12.4 and W08E12.5 belong to a family of putative Metalloproteins which, akin to metallothioneins, may play an important role in Zn-sensing, homeostasis and/or detoxification. |
format | Online Article Text |
id | pubmed-6336089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-63360892019-02-11 Molecular genetic and biochemical characterization of a putative family of zinc metalloproteins in Caenorhabditis elegans Chaudhuri, Poulami Imam, Hasan Tanvir Essig, Yona Krasauskas, Jovaras Webb, Samuel M. Blindauer, Claudia A. Stürzenbaum, Stephen R. Metallomics Chemistry Four highly similar genes (W08E12.2, W08E12.3, W08E12.4 and W08E12.5) which are consecutively aligned on chromosome IV of the C. elegans genome are predicted to code for small (120–141aa) yet cysteine rich (18–19 cysteines) proteins. Cloning and sequencing of the genomic regions of the isoforms confirmed the presence and order of all genes. The generation of transgenic worms strains with an integrated single copy or extrachromosomal multi-copy PW08E12.3;W08E12.4::GFP uncovered that W08E12.3 and W08E12.4 are constitutively expressed in the pharynx and significantly induced in worms exposed to 100 μM Zn. Knockdown by RNAi did not have a marked consequence on reproductive performance nor was a Zn-dependent effect on nematode growth observed. However, RNAi of these genes led to an accumulation of Zn in the intestinal cells. W08E12.3 was recombinantly expressed in E. coli and the purified protein was shown to be able to bind up to 6.5 Zn molecules at neutral pH. Zn-binding was acid-labile and the apo protein was observed at pH < 4.3. This characterization suggests W08E12.2, W08E12.3, W08E12.4 and W08E12.5 belong to a family of putative Metalloproteins which, akin to metallothioneins, may play an important role in Zn-sensing, homeostasis and/or detoxification. Royal Society of Chemistry 2018-12-01 2018-11-16 /pmc/articles/PMC6336089/ /pubmed/30444224 http://dx.doi.org/10.1039/c8mt00169c Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0) |
spellingShingle | Chemistry Chaudhuri, Poulami Imam, Hasan Tanvir Essig, Yona Krasauskas, Jovaras Webb, Samuel M. Blindauer, Claudia A. Stürzenbaum, Stephen R. Molecular genetic and biochemical characterization of a putative family of zinc metalloproteins in Caenorhabditis elegans |
title | Molecular genetic and biochemical characterization of a putative family of zinc metalloproteins in Caenorhabditis elegans
|
title_full | Molecular genetic and biochemical characterization of a putative family of zinc metalloproteins in Caenorhabditis elegans
|
title_fullStr | Molecular genetic and biochemical characterization of a putative family of zinc metalloproteins in Caenorhabditis elegans
|
title_full_unstemmed | Molecular genetic and biochemical characterization of a putative family of zinc metalloproteins in Caenorhabditis elegans
|
title_short | Molecular genetic and biochemical characterization of a putative family of zinc metalloproteins in Caenorhabditis elegans
|
title_sort | molecular genetic and biochemical characterization of a putative family of zinc metalloproteins in caenorhabditis elegans |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336089/ https://www.ncbi.nlm.nih.gov/pubmed/30444224 http://dx.doi.org/10.1039/c8mt00169c |
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