Expression analysis of the plasma membrane H+-ATPase pma4 transcription promoter from Nicotiana plumbaginifolia activated by the CaMV 35S promoter enhancer

Plant Science

Volumn 149, Issue 2, 1999, Pages 157-165

  Zhao, Rongmin ^a   Moriau, Luc ^a   Boutry, Marc ^a  

^a UNIVERSITÉ CATHOLIQUE DE LOUVAIN   (Belgium)

Author keywords

CaMV 35S enhancer; gusA reporter gene; Plasma membrane H+ ATPase; Tissue specific expression; Transcription promoter

Indexed keywords

PROTON TRANSPORTING ADENOSINE TRIPHOSPHATASE;

ARTICLE; ENHANCER REGION; GENE EXPRESSION; GENE SEQUENCE; NONHUMAN; PHYTOCHEMISTRY; PROMOTER REGION; PROTEIN EXPRESSION; TRANSGENIC PLANT;

NICOTIANA PLUMBAGINIFOLIA;

EID: 0033521047     PISSN: 01689452     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0168-9452(99)00155-7     Document Type: Article

References (32)

1. Serrano R. Structure and function of plasma membrane ATPase. Annu. Rev. Plant Physiol. Plant Mol. Biol. 40:1989;61-94.
2. Sussman M.R. Molecular analysis of proteins in the plant plasma membrane. Annu. Rev. Plant Physiol. Plant Mol. Biol. 45:1994;211-234.
3. +-ATPase: a highly regulated enzyme with multiple physiological functions. Plant Physiol. 108:1995;1-6.
4. +-ATPase. Adv. Bot. Res. 28:1998;1-70.
5. +-ATPase multigene family. J. Biol. Chem. 265:1990;13601-13608.
6. +-ATPase in Nicotiana plumbaginifolia. J. Biol. Chem. 267:1992;1204-1211.
7. +-ATPase genes in tomato. Plant Physiol. 106:1994;547-557.
8. Michelet B., Lukaszewicz M., Dupriez V., Boutry M. A plant plasma membrane proton-ATPase gene is regulated by development and environment and shows signs of a translational regulation. Plant Cell. 6:1994;1375-1389.
9. +-ATPase in Nicotiana plumbaginifolia reveals the major transport functions of this enzyme. Plant J. 19:1999;31-41.
10. Balcells L., Coupland G. The presence of enhancers adjacent to the Ac promoter increases the abundance of transposase mRNA and alters the timing of Ds excision in Arabidopsis. Plant Mol. Biol. 24:1994;789-798.
11. Kay R., Chen A., Daly M., McPherson J. Duplication of CaMV 35S promoter sequences creates a strong enhancer for plant genes. Science. 236:1987;1299-1302.
12. Mitsuhara I., Ugaki M., Hirochika H., Ohshima M., Murakami T., Gotoh Y. et al. Efficient promoter cassettes for enhanced expression of foreign genes in dicotyledonous and monocotyledonous plants. Plant Cell Physiol. 37:1996;49-59.
13. Benfey P.N., Ren L., Chua N.-H. The CaMV 35 enhancer contains at least two domains which can confer different development and tissue-specific expression patterns. EMBO J. 8:1989;2199-2202.
14. Benfey P.N., Ren L., Chua N-H. Tissue-specific expression from CaMV 35S enhancer subdomains in early stages of plant development. EMBO J. 9:1990;1677-1684.
15. Benfey P.N., Ren L., Chua N-H. Combinatorial and synergistic properties of CaMV 35S enhancer subdomains. EMBO J. 9:1990;1685-1696.
16. Comai L., Moran P., Maslyar D. Novel and useful properties of a chimeric plant promoter combining CaMV 35S and MAS elements. Plant Mol. Biol. 15:1990;373-381.
17. Ni M., Cui D., Gelvin S.B. Sequence-specific interactions of wound-inducible nuclear factors with mannopine synthase 3′ promoter would-responsive elements. Plant Mol. Biol. 30:1996;77-96.
18. Beilmann A., Albrecht K., Schultze S., Wanner G., Pfitzner U. Activation of a truncated PR-1 promoter by endogenous enhancers in transgenic plants. Plant Mol. Biol. 18:1992;65-78.
19. Fang R-X., Nagy F., Sivasubramaniam S., Chua N-H. Multiple cis regulatory elements for maximal expression of the cauliflower mosaic virus 35S promoter in transgenic plants. Plant Cell. 1:1989;141-150.
20. Omirulleh S., Abraham M., Golovkin M., Stefanov I., Karabaev M.K., Mustardy L. et al. Activity of a chimeric promoter with the doubled CaMV 35S enhancer element in protoplast-derived cells and transgenic plants in maize. Plant Mol. Biol. 21:1993;415-428.
21. Jefferson R.A., Kavanagh T.A, Bevan M.W. Gus fusions: β-Glucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J. 6:1987;3901-3907.
22. Bradford M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72:1976;248-254.
23. An G., Ebert P.R., Mitra A., Ha S.B. Binary vectors. Gelvin S.B., Schilperoort R.A., Verma D.P.S. Plant Molecular Biology Manual. 1988;A3/1-A3/19 Kluwer Academic Publishers, Dordrecht.
24. +-ATPase gene subfamily in Nicotiana plumbaginifolia. Plant Mol. Biol. 21:1993;955-963.
25. Koltunow A.M., Truettner J., Cox K.H., Wallroth M., Goldberg R.B. Different temporal and spatial gene expression patterns occur during anther development. Plant Cell. 2:1990;1201-1224.
26. Guerrero F.D., Crossland L., Smutzer G.S., Hamilton D.A., Mascarenhas J.P. Promoter sequences from a maize pollen-specific gene direct tissue-specific transcription in tobacco. Mol. Gen. Genet. 224:1990;161-168.
27. Plegt L., Bino R.J. Glucuronidase activity during development of the male gametophyte from transgenic and non-transgenic plants. Mol. Gen. Genet. 216:1989;321-327.
28. Holtorf S., Apel K., Bohlmann H. Comparison of different constitutive and inducible promoters for the overexpression of transgenes in Arabidopsis thaliana. Plant Mol. Biol. 29:1995;637-646.
29. Vaucheret H., Béclin C., Elmayan T., Feuerbach F., Godon C., Morel J-B. et al. Transgene-induced gene silencing in plants. Plant J. 16:1998;651-659.
30. Matzke M.A., Matzke A.J.M. How and why do plants inactivate homologous (trans)genes? Plant Physiol. 107:1995;679-685.
31. Crete P., Caboche M., Meyer C. Nitrate reductase expression is regulated at the post-transcriptional level by the nitrogen source in Nicotiana plumbaginifolia and Arabidopsis thaliana. Plant J. 1:1997;625-634.
32. +-ATPase that confers acid resistance in Arabidopsis thaliana seedlings. Genetics. 149:1998;501-507.