A systemic gene silencing method suitable for high throughput, reverse genetic analyses of gene function in fern gametophytes

被引:38
作者
Rutherford G. [1 ]
Tanurdzic M. [1 ,2 ]
Hasebe M. [3 ]
Banks J.A. [1 ,2 ,3 ]
机构
[1] Dept. of Botany and Plant Pathology, Purdue University, West Lafayette
[2] Purdue Genetics Program, Purdue University, West Lafayette
[3] National Institute for Basic Biology
关键词
Gene Silence; Induce Gene Silence; Fern Gametophyte; Magnesium Chelatase; Inverted Repeat Construct;
D O I
10.1186/1471-2229-4-6
中图分类号
学科分类号
摘要
Background: Ceratopteris richardii is a useful experimental system for studying gametophyte development and sexual reproduction in plants. However, few tools for cloning mutant genes or disrupting gene function exist for this species. The feasibility of systemic gene silencing as a reverse genetics tool was examined in this study. Results: Several DNA constructs targeting a Ceratopteris protoporphyrin IX magnesium chelatase (CrChlI) gene that is required for chlorophyll biosynthesis were each introduced into young gametophytes by biolistic delivery. Their transient expression in individual cells resulted in a colorless cell phenotype that affected most cells of the mature gametophyte, including the meristem and gametangia. The colorless phenotype was associated with a 7-fold decrease in the abundance of the endogenous transcript. While a construct designed to promote the transient expression of a CrChlI double stranded, potentially hairpin-forming RNA was found to be the most efficient in systemically silencing the endogenous gene, a plasmid containing the CrChlI cDNA insert alone was sufficient to induce silencing. Bombarded, colorless hermaphroditic gametophytes produced colorless embryos following self-fertilization, demonstrating that the silencing signal could be transmitted through gametogenesis and fertilization. Bombardment of young gametophytes with constructs targeting the Ceratopteris filamentous temperature sensitive (CrFtsZ) and uroporphyrin dehydrogenase (CrUrod) genes also produced the expected mutant phenotypes. Conclusion: A method that induces the systemic silencing of target genes in the Ceratopteris gametophyte is described. It provides a simple, inexpensive and rapid means to test the functions of genes involved in gametophyte development, especially those involved in cellular processes common to all plants.
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页数:30
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共 41 条
[1]  
Chatterjee A., Roux S.J., Ceratopteris richardii: A productive model for revealing secrets of signaling and development, J Plant Growth Regul, 19, pp. 284-289, (2000)
[2]  
Banks J.A., Hickok L., Webb M.A., The Programming of Sexual Phenotype in the Homosporous Fern Ceratopteris-Richardii, International Journal of Plant Sciences, 154, pp. 522-534, (1993)
[3]  
Banks J.A., The TRANSFORMER genes of the fern Ceratopteris simultaneously promote meristem and archegonia development and repress antheridia development in the developing gametophyte, Genetics, 147, pp. 1885-1897, (1997)
[4]  
Strain E., Hass B., Banks J.A., Characterization of mutations that feminize gametophytes of the fern Ceratopteris, Genetics, 159, pp. 1271-1281, (2001)
[5]  
Banks J.A., Gametophyte development in ferns, Annual Review of Plant Physiology and Plant Molecular Biology, 50, (1999)
[6]  
Ashrafi K., Chang F.Y., Watts J.L., Fraser A.G., Kamath R.S., Ahringer J., Ruvkun G., Genome-wide RNAi analysis of Caenorhabditis elegans fat regulatory genes, Nature, 421, pp. 268-272, (2003)
[7]  
Chuang C.F., Meyerowitz E.M., Specific and heritable genetic interference by double-stranded RNA in Arabidopsis thaliana, Proceedings of the National Academy of Sciences of the United States of America, 97, pp. 4985-4990, (2000)
[8]  
Fraser A.G., Kamath R.S., Zipperlen P., Martinez-Campos M., Sohrmann M., Ahringer J., Functional genomic analysis of C. elegans chromosome I by systematic RNA interference, Nature, 408, pp. 325-330, (2000)
[9]  
Gonczy P., Echeverri C., Oegema K., Coulson A., Jones S.J., Copley R.R., Duperon J., Oegema J., Brehm M., Cassin E., Hannak E., Kirkham M., Pichler S., Flohrs K., Goessen A., Leidel S., Alleaume A.M., Martin C., Ozlu N., Bork P., Hyman A.A., Functional genomic analysis of cell division in C. elegans using RNAi of genes on chromosome III, Nature, 408, pp. 331-336, (2000)
[10]  
Maeda I., Kohara Y., Yamamoto M.Y., Sugimoto A., Large-scale analysis of gene function in Caenorhabditis elegans by high-throughput RNAi, Curr Biol, 11, pp. 171-176, (2001)