Yann Desfougères , Paloma Portela-Torres , Danye Qiu , Thomas M. Livermore , Robert K. Harmel , Filipy Borghi , Henning J. Jessen , Dorothea Fiedler , Adolfo Saiardi
{"title":"Dictyostelium disideum的肌醇焦磷酸盐代谢不调节无机多磷酸盐(polyP)的合成","authors":"Yann Desfougères , Paloma Portela-Torres , Danye Qiu , Thomas M. Livermore , Robert K. Harmel , Filipy Borghi , Henning J. Jessen , Dorothea Fiedler , Adolfo Saiardi","doi":"10.1016/j.jbior.2021.100835","DOIUrl":null,"url":null,"abstract":"<div><p>Initial studies on the inositol phosphates metabolism were enabled by the social amoeba <em>Dictyostelium discoideum.</em> The abundant amount of inositol hexakisphosphate (IP<sub>6</sub> also known as Phytic acid) present in the amoeba allowed the discovery of the more polar inositol pyrophosphates, IP<sub>7</sub> and IP<sub>8</sub>, possessing one or two high energy phosphoanhydride bonds, respectively. Considering the contemporary growing interest in inositol pyrophosphates, it is surprising that in recent years <em>D. discoideum</em>, has contributed little to our understanding of their metabolism and function. This work fulfils this lacuna, by analysing the <em>ip6k, ppip5k</em> and <em>ip6k-ppip5K</em> amoeba null strains using PAGE, <sup>13</sup>C-NMR and CE-MS analysis. Our study reveals an inositol pyrophosphate metabolism more complex than previously thought. The amoeba Ip6k synthesizes the 4/6-IP<sub>7</sub> in contrast to the 5-IP<sub>7</sub> isomer synthesized by the mammalian homologue. The amoeba Ppip5k synthesizes the same 1/3-IP<sub>7</sub> as the mammalian enzyme. In <em>D. discoideum</em>, the <em>ip6k</em> strain possesses residual amounts of IP<sub>7</sub>. The residual IP<sub>7</sub> is also present in the <em>ip6k-ppip5K</em> strain, while the <em>ppip5k</em> single mutant shows a decrease in both IP<sub>7</sub> and IP<sub>8</sub> levels. This phenotype is in contrast to the increase in IP<sub>7</sub> observable in the yeast <em>vip1</em>Δ strain. The presence of IP<sub>8</sub> in <em>ppip5k</em> and the presence of IP<sub>7</sub> in <em>ip6k-ppip5K</em> indicate the existence of an additional inositol pyrophosphate synthesizing enzyme. Additionally, we investigated the existence of a metabolic relationship between inositol pyrophosphate synthesis and inorganic polyphosphate (polyP) metabolism as observed in yeast. These studies reveal that contrary to the yeast, Ip6k and Ppip5k do not control polyP cellular level in amoeba.</p></div>","PeriodicalId":7214,"journal":{"name":"Advances in biological regulation","volume":"83 ","pages":"Article 100835"},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8885430/pdf/","citationCount":"5","resultStr":"{\"title\":\"The inositol pyrophosphate metabolism of Dictyostelium discoideum does not regulate inorganic polyphosphate (polyP) synthesis\",\"authors\":\"Yann Desfougères , Paloma Portela-Torres , Danye Qiu , Thomas M. Livermore , Robert K. Harmel , Filipy Borghi , Henning J. Jessen , Dorothea Fiedler , Adolfo Saiardi\",\"doi\":\"10.1016/j.jbior.2021.100835\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Initial studies on the inositol phosphates metabolism were enabled by the social amoeba <em>Dictyostelium discoideum.</em> The abundant amount of inositol hexakisphosphate (IP<sub>6</sub> also known as Phytic acid) present in the amoeba allowed the discovery of the more polar inositol pyrophosphates, IP<sub>7</sub> and IP<sub>8</sub>, possessing one or two high energy phosphoanhydride bonds, respectively. Considering the contemporary growing interest in inositol pyrophosphates, it is surprising that in recent years <em>D. discoideum</em>, has contributed little to our understanding of their metabolism and function. This work fulfils this lacuna, by analysing the <em>ip6k, ppip5k</em> and <em>ip6k-ppip5K</em> amoeba null strains using PAGE, <sup>13</sup>C-NMR and CE-MS analysis. Our study reveals an inositol pyrophosphate metabolism more complex than previously thought. The amoeba Ip6k synthesizes the 4/6-IP<sub>7</sub> in contrast to the 5-IP<sub>7</sub> isomer synthesized by the mammalian homologue. The amoeba Ppip5k synthesizes the same 1/3-IP<sub>7</sub> as the mammalian enzyme. In <em>D. discoideum</em>, the <em>ip6k</em> strain possesses residual amounts of IP<sub>7</sub>. The residual IP<sub>7</sub> is also present in the <em>ip6k-ppip5K</em> strain, while the <em>ppip5k</em> single mutant shows a decrease in both IP<sub>7</sub> and IP<sub>8</sub> levels. This phenotype is in contrast to the increase in IP<sub>7</sub> observable in the yeast <em>vip1</em>Δ strain. The presence of IP<sub>8</sub> in <em>ppip5k</em> and the presence of IP<sub>7</sub> in <em>ip6k-ppip5K</em> indicate the existence of an additional inositol pyrophosphate synthesizing enzyme. Additionally, we investigated the existence of a metabolic relationship between inositol pyrophosphate synthesis and inorganic polyphosphate (polyP) metabolism as observed in yeast. These studies reveal that contrary to the yeast, Ip6k and Ppip5k do not control polyP cellular level in amoeba.</p></div>\",\"PeriodicalId\":7214,\"journal\":{\"name\":\"Advances in biological regulation\",\"volume\":\"83 \",\"pages\":\"Article 100835\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8885430/pdf/\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advances in biological regulation\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2212492621000518\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"Biochemistry, Genetics and Molecular Biology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in biological regulation","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2212492621000518","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
The inositol pyrophosphate metabolism of Dictyostelium discoideum does not regulate inorganic polyphosphate (polyP) synthesis
Initial studies on the inositol phosphates metabolism were enabled by the social amoeba Dictyostelium discoideum. The abundant amount of inositol hexakisphosphate (IP6 also known as Phytic acid) present in the amoeba allowed the discovery of the more polar inositol pyrophosphates, IP7 and IP8, possessing one or two high energy phosphoanhydride bonds, respectively. Considering the contemporary growing interest in inositol pyrophosphates, it is surprising that in recent years D. discoideum, has contributed little to our understanding of their metabolism and function. This work fulfils this lacuna, by analysing the ip6k, ppip5k and ip6k-ppip5K amoeba null strains using PAGE, 13C-NMR and CE-MS analysis. Our study reveals an inositol pyrophosphate metabolism more complex than previously thought. The amoeba Ip6k synthesizes the 4/6-IP7 in contrast to the 5-IP7 isomer synthesized by the mammalian homologue. The amoeba Ppip5k synthesizes the same 1/3-IP7 as the mammalian enzyme. In D. discoideum, the ip6k strain possesses residual amounts of IP7. The residual IP7 is also present in the ip6k-ppip5K strain, while the ppip5k single mutant shows a decrease in both IP7 and IP8 levels. This phenotype is in contrast to the increase in IP7 observable in the yeast vip1Δ strain. The presence of IP8 in ppip5k and the presence of IP7 in ip6k-ppip5K indicate the existence of an additional inositol pyrophosphate synthesizing enzyme. Additionally, we investigated the existence of a metabolic relationship between inositol pyrophosphate synthesis and inorganic polyphosphate (polyP) metabolism as observed in yeast. These studies reveal that contrary to the yeast, Ip6k and Ppip5k do not control polyP cellular level in amoeba.