JIANG Ting-Bo, DING Bao-Jian, LI Feng-Juan, YANG Chuan-Ping
{"title":"过表达大豆铁蛋白基因转基因烟草内源铁蛋白基因差异表达及铁稳态改变","authors":"JIANG Ting-Bo, DING Bao-Jian, LI Feng-Juan, YANG Chuan-Ping","doi":"10.1016/S0379-4172(06)60150-9","DOIUrl":null,"url":null,"abstract":"<div><p>For studying the effects of endogenous ferritin gene expressions (<em>NtFer1</em>, GenBank accession number ay083924; and <em>NtFer2</em>, GenBank accession number ay141105) on the iron homeostasis in transgenic tobacco (<em>Nicotiana tabacum</em> L.) plants expressing soybean (<em>Glycine max</em> Merr) ferritin gene (<em>SoyFer1</em>, GenBank accession number m64337), the transgenic tobacco has been produced by placing soybean ferritin cDNA cassette under the control of the CaMV 35S promoter. The exogenous gene expression was examined by both Northern- and Western-blot analyses. Comparison of endogenous ferritin gene expressions between nontransformant and transgenic tobacco plants showed that the expression of <em>NtFer1</em> was increased in the leaves of transgenic tobacco plants, whereas the <em>NtFer2</em> expression was unchanged. The iron concentration in the leaves of transgenic tobacco plants was about 1.5-folds higher than that in nontransformant. Enhanced growth of transgenic tobacco was observed at the early development stages, resulting in plant height and fresh weights significantly greater than those in the nontransformant. These results demonstrated that exogenous ferritin expression induced increased expression of at least one of the endogenous ferritin genes in transgenic tobacco plants by enhancing the ferric chelate reductase activity and iron transport ability of the root, and improved the rate of photosynthesis.</p></div>","PeriodicalId":100017,"journal":{"name":"Acta Genetica Sinica","volume":"33 12","pages":"Pages 1120-1126"},"PeriodicalIF":0.0000,"publicationDate":"2006-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0379-4172(06)60150-9","citationCount":"11","resultStr":"{\"title\":\"Differential Expression of Endogenous Ferritin Genes and Iron Homeostasis Alteration in Transgenic Tobacco Overexpressing Soybean Ferritin Gene\",\"authors\":\"JIANG Ting-Bo, DING Bao-Jian, LI Feng-Juan, YANG Chuan-Ping\",\"doi\":\"10.1016/S0379-4172(06)60150-9\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>For studying the effects of endogenous ferritin gene expressions (<em>NtFer1</em>, GenBank accession number ay083924; and <em>NtFer2</em>, GenBank accession number ay141105) on the iron homeostasis in transgenic tobacco (<em>Nicotiana tabacum</em> L.) plants expressing soybean (<em>Glycine max</em> Merr) ferritin gene (<em>SoyFer1</em>, GenBank accession number m64337), the transgenic tobacco has been produced by placing soybean ferritin cDNA cassette under the control of the CaMV 35S promoter. The exogenous gene expression was examined by both Northern- and Western-blot analyses. Comparison of endogenous ferritin gene expressions between nontransformant and transgenic tobacco plants showed that the expression of <em>NtFer1</em> was increased in the leaves of transgenic tobacco plants, whereas the <em>NtFer2</em> expression was unchanged. The iron concentration in the leaves of transgenic tobacco plants was about 1.5-folds higher than that in nontransformant. Enhanced growth of transgenic tobacco was observed at the early development stages, resulting in plant height and fresh weights significantly greater than those in the nontransformant. These results demonstrated that exogenous ferritin expression induced increased expression of at least one of the endogenous ferritin genes in transgenic tobacco plants by enhancing the ferric chelate reductase activity and iron transport ability of the root, and improved the rate of photosynthesis.</p></div>\",\"PeriodicalId\":100017,\"journal\":{\"name\":\"Acta Genetica Sinica\",\"volume\":\"33 12\",\"pages\":\"Pages 1120-1126\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2006-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S0379-4172(06)60150-9\",\"citationCount\":\"11\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta Genetica Sinica\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0379417206601509\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Genetica Sinica","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0379417206601509","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 11
摘要
为了研究内源性铁蛋白基因表达的影响(NtFer1, GenBank登录号ay083924;大豆(Glycine max Merr)铁蛋白基因(SoyFer1, GenBank登录号m64337)在转基因烟草(Nicotiana tabacum L.)植株中表达铁蛋白基因(SoyFer1, GenBank登录号m64337),通过将大豆铁蛋白cDNA盒置于CaMV 35S启动子调控下获得转基因烟草。通过Northern- blot和Western-blot检测外源基因的表达。比较未转化和转基因烟草植株内源铁蛋白基因的表达情况发现,转基因烟草植株叶片中NtFer1的表达增加,而NtFer2的表达不变。转基因烟草叶片中的铁含量是未转基因烟草叶片的1.5倍左右。在烟草发育早期,转基因烟草的生长得到增强,株高和鲜重均显著高于未转化烟草。上述结果表明,外源铁蛋白表达通过提高烟草根系铁螯合还原酶活性和铁转运能力,诱导至少一种内源铁蛋白基因的表达增加,提高了烟草光合速率。
Differential Expression of Endogenous Ferritin Genes and Iron Homeostasis Alteration in Transgenic Tobacco Overexpressing Soybean Ferritin Gene
For studying the effects of endogenous ferritin gene expressions (NtFer1, GenBank accession number ay083924; and NtFer2, GenBank accession number ay141105) on the iron homeostasis in transgenic tobacco (Nicotiana tabacum L.) plants expressing soybean (Glycine max Merr) ferritin gene (SoyFer1, GenBank accession number m64337), the transgenic tobacco has been produced by placing soybean ferritin cDNA cassette under the control of the CaMV 35S promoter. The exogenous gene expression was examined by both Northern- and Western-blot analyses. Comparison of endogenous ferritin gene expressions between nontransformant and transgenic tobacco plants showed that the expression of NtFer1 was increased in the leaves of transgenic tobacco plants, whereas the NtFer2 expression was unchanged. The iron concentration in the leaves of transgenic tobacco plants was about 1.5-folds higher than that in nontransformant. Enhanced growth of transgenic tobacco was observed at the early development stages, resulting in plant height and fresh weights significantly greater than those in the nontransformant. These results demonstrated that exogenous ferritin expression induced increased expression of at least one of the endogenous ferritin genes in transgenic tobacco plants by enhancing the ferric chelate reductase activity and iron transport ability of the root, and improved the rate of photosynthesis.