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Exploring valid internal-control genes in Porphyra yezoensis (Bangiaceae) during stress response conditions
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  • 作者:Wenlei Wang (1)
    Xiaojie Wu (1)
    Chao Wang (2)
    Zhaojun Jia (1)
    Linwen He (2)
    Yifan Wei (2)
    Jianfeng Niu (2) (3)
    Guangce Wang (1) (2)
  • 关键词:constitutive expression gene ; housekeeping gene ; Porphyra yezoensis Ueda ; real ; time quantitative PCR ; stress responding
  • 刊名:Chinese Journal of Oceanology and Limnology
  • 出版年:2014
  • 出版时间:July 2014
  • 年:2014
  • 卷:32
  • 期:4
  • 页码:783-791
  • 全文大小:586 KB
  • 参考文献:1. Andersen C L, Jensen J L, rntoft T F. 2004. Normalization of real-time quantitative reverse transcription-PCR data: a model-based variance estimation approach to identify genes suited for normalization, applied to bladder and colon cancer data sets. / Cancer Re search, 64: 5 245- 250. CrossRef
    2. Axelos M, Bardet C, Liboz T, Le Van Thai A, Curie C, Lescure B. 1989. The gene family encoding the / Arabidopsis thaliana translation elongation factor EF-lα: molecular cloning, characterization and expression. / Molecular Genetics and Genomics, 219: 106-12.
    3. Beer S, Larsson C, Poryan O, Axelsson L. 2000. Photosynthetic rates of / Ulva (Chlorophyta) measured by pulse amplitude modulated (PAM) fluorometry. / European Journal of Phycology, 35: 69-4. CrossRef
    4. Binet M, Weil J, Tessier L. 1991. Structure and expression of sunflower ubiquitin genes. / Plant Molecular Biology, 17: 395-07. CrossRef
    5. Blouin N A, Brodie J A, Grossman A C, Xu P, Brawley S H. 2010. / Porphyra: a marine crop shaped by stress. / Trends in Plant Science, 16: 29-7. CrossRef
    6. Bustin S A. 2000. Absolute quantification of mRNA using realtime reverse transcription polymerase chain reaction assays. / Journal of Molecular Endocrinology, 25: 169-93. CrossRef
    7. Bustin S A. 2002. Quantification of mRNA using real-time reverse transcription PCR (RT-PCR): trends and problems. / Journal of Molecular Endocrinology, 29: 23-9. CrossRef
    8. Christensen A H, Quail P H. 1989. Sequence analysis and transcriptional regulation by heat shock of polyubiquitin transcripts from maize. / Plant Molecular Biology, 12: 619-32. CrossRef
    9. Dharmawardhane S, Demma M, Yang F, Condeelis J. 1991. Compartmentalization and actin binding-properties of ABP-50-the elongation factor-1alpha of / Dictyostelium. Cell Motil Cytoskeleton, 20: 279-88. CrossRef
    10. Gao S, Wang G. 2012. The enhancement of cyclic electron flow around photosystem I improves the recovery of severely desiccated / Porphyra yezoensis (Bangiales, Rhodophyta). / Journal of E xperimental B otany, 63: 4 349- 358.
    11. Genty B, Briantais J M, Baker N R. 1989. The relationship between the quantum yield of photosynthetic electrontransport and quenching of chlorophyll fluorescence. / Biochimica et Biophysica Acta, 990: 87-2. CrossRef
    12. Jain M A, Nijhawan A, Tyagi A K, Khurana J P. 2006. Validation of housekeeping genes as internal control for studying gene expression in rice by quantitative real-time PCR. / Biochemical and Biophysical Research Communications, 345: 646-51. CrossRef
    13. Kawasaki S, Borchert C, Deyholos M, Wang H, Brazille S, Kawai K, Galbraith D, Bohnert H J. 2001. Gene expression profiles during the initial phase of salt stress in rice. / The Plant Cell, 13: 889-05. CrossRef
    14. Marri L, Sparla F, Pupillo P, Trost P. 2005. Co-ordinated gene expression of photosynthetic glyceraldehyde-3-phosphate dehydrogenase, phosphoribulokinase, and CP12 in / Arabidopsis thaliana. / Journal of Experimental Botany, 56: 73-0.
    15. quist G, Fork D C. 1982. Effects of desiccation on the excitation energy distribution from phycoerythrin to the two photosystems in the red alga Porphyra perforata. / Physiologia Plantarum, 56: 56-2. CrossRef
    16. Ostrem J A, Vernon D M, Bohnert H J. 1990. Increased expression of a gene coding for NAD: glyceraldehyde-3-phosphate dehydrogenase during the transition from C3 photosynthesis to crassulacean acid metabolism in / Mesembryanthemum crystallinum. / Journal of Biochemistry and Molecular Biology, 265: 3 497- 502.
    17. Prasil O, Suggett D J, Cullen J J, Govindjee B M. 2008. Aquafluo 2007: chlorophyll fluorescence in aquatic sciences, an international conference held in Nové Hrady. / Photosynthesis Research, 95: 111-15. CrossRef
    18. Russell D A, Sachs M M. 1989. Differential expression and sequence analysis of the maize glyceraldehyde-3-phosphate dehydrogenase gene family. / The Plant Cell, 1: 793-03. CrossRef
    19. Schreiber U, Schliwa U, Bilger W. 1986. Continuous recording of photochemical and non-photochemical chlorophyll fluorescence quenching with a new type of modulation fluorometer. / Photosynthesis Research, 10: 51-2. CrossRef
    20. Setter T L, Flannigan B A. 2001. Water deficit inhibits cell division and expression of transcripts involved in cell proliferation and endoreduplication in maize endosperm. / Journal of Experimental Botany, 52: 1 401- 408. CrossRef
    21. Suzuki T, Higgins P J, Crawford D R. 2000. Control selection for RNA quantitation. / Biotechniques, 29: 332-37.
    22. Vandesompele J, De Preter K, Pattyn F, Poppe B, Van Roy N, Paepe A D, Speleman F. 2002. Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. / Genome Biology, 3: RESEARCH0034. CrossRef
    23. Whelan J A, Russell N B, Whelan M A. 2003. A method for the absolute quantification of cDNA using real-time PCR. / Journal of Immunological Methods, 278: 261-69. CrossRef
    24. Wong M L, Medrano J F. 2005. Real-time PCR for mRNA quantitation. / BioTechniques, 39: 75-5. CrossRef
  • 作者单位:Wenlei Wang (1)
    Xiaojie Wu (1)
    Chao Wang (2)
    Zhaojun Jia (1)
    Linwen He (2)
    Yifan Wei (2)
    Jianfeng Niu (2) (3)
    Guangce Wang (1) (2)

    1. College of Marine Science and Engineering, Tianjin University of Science and Technology, Tianjin, 300457, China
    2. Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China
    3. Nantong Branch, Institute of Oceanology, Chinese Academy of Sciences, Nantong, 226006, China
  • ISSN:1993-5005
文摘
To screen the stable expression genes related to the stress (strong light, dehydration and temperature shock) we applied Absolute real-time PCR technology to determine the transcription numbers of the selected test genes in P orphyra yezoensis, which has been regarded as a potential model species responding the stress conditions in the intertidal. Absolute real-time PCR technology was applied to determine the transcription numbers of the selected test genes in P orphyra yezoensis, which has been regarded as a potential model species in stress responding. According to the results of photosynthesis parameters, we observed that Y(II) and F v/F m were significantly affected when stress was imposed on the thalli of P orphyra yezoensis, but underwent almost completely recovered under normal conditions, which were collected for the following experiments. Then three samples, which were treated with different grade stresses combined with salinity, irradiation and temperature, were collected. The transcription numbers of seven constitutive expression genes in above samples were determined after RNA extraction and cDNA synthesis. Finally, a general insight into the selection of internal control genes during stress response was obtained. We found that there were no obvious effects in terms of salinity stress (at salinity 90) on transcription of most genes used in the study. The 18S ribosomal RNA gene had the highest expression level, varying remarkably among different tested groups. RPS8 expression showed a high irregular variance between samples. GAPDH presented comparatively stable expression and could thus be selected as the internal control. EF-1α showed stable expression during the series of multiple-stress tests. Our research provided available references for the selection of internal control genes for transcripts determination of P. yezoensis.

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