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Phosphatidylinositol 4-phosphate 5-kinase Iγ_v6, a new splice variant found in rodents and humans
Phosphatidylinositol 4-phosphate 5-kinase Iγ (PIP5KIγ) is subject to extensive C-terminal splice variation, with four variants, PIP5KIγ_v1, 2, 4 and 5, described in humans Schill and Anderson (2009) [7]. Here firstly, we report a new rodent splice variant, which includes the exon that was previously...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Academic Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3176900/ https://www.ncbi.nlm.nih.gov/pubmed/21756881 http://dx.doi.org/10.1016/j.bbrc.2011.06.168 |
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author | Xia, Yang Irvine, Robin F. Giudici, Maria-Luisa |
author_facet | Xia, Yang Irvine, Robin F. Giudici, Maria-Luisa |
author_sort | Xia, Yang |
collection | PubMed |
description | Phosphatidylinositol 4-phosphate 5-kinase Iγ (PIP5KIγ) is subject to extensive C-terminal splice variation, with four variants, PIP5KIγ_v1, 2, 4 and 5, described in humans Schill and Anderson (2009) [7]. Here firstly, we report a new rodent splice variant, which includes the exon that was previously unique to the rodent neuron-specific PIP5KIγ93 Giudici et al. (2006) [6], but which omits the C-terminal exon of PIP5KIγ93; this new variant shows a wide tissue expression pattern in mouse. Secondly, we show that in humans there is an alternative splicing site 78 nucleotides from the start of exon 16c, such that humans additionally express both PIP5KIγ93 (which we now call PIP5KIγ_v3) specifically in brain and, again expressed more widely, the new variant described here, which we now name PIP5KIγ_v6. |
format | Online Article Text |
id | pubmed-3176900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Academic Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-31769002011-10-03 Phosphatidylinositol 4-phosphate 5-kinase Iγ_v6, a new splice variant found in rodents and humans Xia, Yang Irvine, Robin F. Giudici, Maria-Luisa Biochem Biophys Res Commun Article Phosphatidylinositol 4-phosphate 5-kinase Iγ (PIP5KIγ) is subject to extensive C-terminal splice variation, with four variants, PIP5KIγ_v1, 2, 4 and 5, described in humans Schill and Anderson (2009) [7]. Here firstly, we report a new rodent splice variant, which includes the exon that was previously unique to the rodent neuron-specific PIP5KIγ93 Giudici et al. (2006) [6], but which omits the C-terminal exon of PIP5KIγ93; this new variant shows a wide tissue expression pattern in mouse. Secondly, we show that in humans there is an alternative splicing site 78 nucleotides from the start of exon 16c, such that humans additionally express both PIP5KIγ93 (which we now call PIP5KIγ_v3) specifically in brain and, again expressed more widely, the new variant described here, which we now name PIP5KIγ_v6. Academic Press 2011-07-29 /pmc/articles/PMC3176900/ /pubmed/21756881 http://dx.doi.org/10.1016/j.bbrc.2011.06.168 Text en © 2011 Elsevier Inc. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
spellingShingle | Article Xia, Yang Irvine, Robin F. Giudici, Maria-Luisa Phosphatidylinositol 4-phosphate 5-kinase Iγ_v6, a new splice variant found in rodents and humans |
title | Phosphatidylinositol 4-phosphate 5-kinase Iγ_v6, a new splice variant found in rodents and humans |
title_full | Phosphatidylinositol 4-phosphate 5-kinase Iγ_v6, a new splice variant found in rodents and humans |
title_fullStr | Phosphatidylinositol 4-phosphate 5-kinase Iγ_v6, a new splice variant found in rodents and humans |
title_full_unstemmed | Phosphatidylinositol 4-phosphate 5-kinase Iγ_v6, a new splice variant found in rodents and humans |
title_short | Phosphatidylinositol 4-phosphate 5-kinase Iγ_v6, a new splice variant found in rodents and humans |
title_sort | phosphatidylinositol 4-phosphate 5-kinase iγ_v6, a new splice variant found in rodents and humans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3176900/ https://www.ncbi.nlm.nih.gov/pubmed/21756881 http://dx.doi.org/10.1016/j.bbrc.2011.06.168 |
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