The 90 kDa heat shock protein (hsp90) is expressed throughout Brassica napus seed development and germination

Plant Science

Volumn 131, Issue 2, 1998, Pages 131-137

  Reddy, Ramachandra K ^b   Chaudhary, Sarita ^a   Patil, Prashant ^b   Krishna, Priti ^b  

^a UNIVERSITY OF CALGARY   (Canada)

^b NONE

Author keywords

Brassica napus; Germination; Hsp90; Seed development

Indexed keywords

BRASSICA; CHAPERONE; HEAT SHOCK PROTEIN; POLLEN;

ARTICLE; GENE EXPRESSION; GERMINATION; PLANT SEED; PROTEIN ANALYSIS; PROTEIN BINDING; PROTEIN CONFORMATION; STRESS;

BRASSICA NAPUS;

EID: 0032472817     PISSN: 01689452     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0168-9452(97)00254-9     Document Type: Article

References (33)

1. Hendrick J.P., Hartl F-U. Molecular chaperone functions of heat-shock proteins. Annu. Rev. Biochem. 62:1993;349-384.
2. Pratt W.B. The role of heat shock proteins in regulating the function, folding and trafficking of the glucocorticoid receptor. J. Biol. Chem. 268:1993;21455-21458.
3. Picard D., Khursheed B., Garabedian M.J., Fortin M.G., Lindquist S., Yamamoto K.R. Reduced levels of hsp90 compromise steroid receptor action in vivo. Nature. 348:1990;166-168.
4. Sanchez E.R., Toft D.O., Schlesinger M.J., Pratt W.B. Evidence that the 90-kDa phosphoprotein associated with the untransformed L-cell glucocorticoid receptor is a murine heat shock protein. J. Biol. Chem. 260:1985;12398-12401.
5. Aligue A., Akhavan-Niak H., Russell P. A role for hsp90 in cell cycle control: Wee 1 tyrosine kinase activity requires interaction with hsp90. EMBO J. 13:1994;6099-6106.
6. src with the cellular proteins pp50 and pp90. Curr. Top. Microbiol. Immunol. 123:1986;1-22.
7. Miyata Y., Yahara I. The 90-kDa heat shock protein, HSP90, binds and protects casein kinase II from self-aggregation and enhances its kinase activity. J. Biol. Chem. 267:1992;7042-7047.
8. Rose D.W., Welch W.J., Kramer G., Hardesty B. Possible involvement of the 90-kDa heat shock protein in the regulation of protein synthesis. J. Biol. Chem. 264:1989;6239-6244.
9. Jakob U., Lilie H., Meyer I., Buchner J. Transient interaction of hsp90 with early unfolding intermediates of citrate synthase. Implications for heat shock in vivo. J. Biol Chem. 270:1995;7288-7294.
10. Conner T.W., Lafayette P.R., Nagao R.T, Key J.L. Sequence and expression of a HSP83 from Arabidopsis thaliana. Plant Physiol. 94:1990;1689-1695.
11. Felsheim R.F., Das A. Structure and expression of a heat-shock protein 83 gene of Pharbitis nil. Plant Physiol. 100:1992;1764-1771.
12. Koning A.J., Rose R., Comai L. Developmental expression of tomato heat-shock cognate protein 80. Plant Physiol. 100:1992;801-811.
13. Krishna P., Sacco M., Cherutti J.F., Hill S. Cold-induced accumulation of hsp90 transcripts in Brassica napus. Plant Physiol. 107:1995;915-923.
14. Marrs K.A.E., Casey E.S., Capitant S.A., Bouchard R.A., Dietrich P.S., Mettler I.J., Sinibaldi R.M. Characterization of two maize hsp90 heat shock protein genes and expression during heat shock, embryogenesis and pollen development. Dev. Genet. 14:1993;27-41.
15. Yabe N., Takahashi T., Komeda Y. Analysis of tissue-specific expression of Arabidopsis thaliana hsp90-family gene HSP81. Plant Cell Physiol. 35:1994;1207-1219.
16. Schroder G., Beck M., Eichel J., Vetter H-P., Schroder J. Hsp90 homologue from Madagascar periwinkle (Catharanthus roseus): cDNA sequence, regulation of protein expression and location in the endoplasmic reticulum. Plant Mol. Biol. 23:1993;583-594.
17. Schmitz G., Schmidt M., Feierabend J. Characterization of a plastid-specific HSP90 homologue: identification of a cDNA sequence, phylogenetic descendence and analysis of its mRNA and protein expression. Plant Mol. Biol. 30:1996;479-492.
18. Owens-Grillo J.K., Stancato L.F., Hoffmann K., Pratt W.B., Krishna P. Binding of immunophilins to the 90 kDa heat shock protein (hsp90) via a tetratricopeptide repeat domain is a conserved protein interaction in plants. Biochemistry. 35:1996;15249-15255.
19. Stancato L.F., Hutchison K.A., Krishna P., Pratt W.B. Animal and plant-cell lysates share a conserved chaperone system that assembles the glucocorticoid receptor into a functional heterocomplex with hsp90. Biochemistry. 35:1996;554-561.
20. Li J., Nagpal P., Vitart V., McMorris T.C., Chory J. A role for brassinosteroids in light-dependent development of Arabidopsis. Science. 272:1996;398-401.
21. Zimmerman J.L., Petri W., Meselson M. Accumulation of a specific subset of D. melanogaster heat shock mRNAs in normal development without heat shock. Cell. 32:1983;1161-1170.
22. Laemmli U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 227:1970;680-685.
23. Ko K., Bornemisza O., Kourtz L., Ko Z.W., Plaxton W.C., Cashmore A.R. Isolation and characterization of a cDNA clone encoding a cognate 70 kDa heat shock protein of the chloroplast envelop. J. Biol. Chem. 267:1992;2986-2993.
24. Domoney C., Ellis N., Turner L., Casey R. A developmentally regulated early-embryogenesis protein in pea (Pisum sativum L.) is related to the heat-shock protein (hsp70) gene family. Planta. 184:1991;350-355.
25. Crouch M.L., Sussex I.M. Development and storage-protein synthesis in Brassica napus L. embryos in vivo and in vitro. Planta. 153:1981;64-74.
26. Jerome V., Vourc'h C., Baulieu E-E., Catelli M-G. Cell cycle regulation of the chicken hsp90α expression. Exp. Cell Res. 205:1993;44-51.
27. Pareek A., Singla S.L., Kush A.K., Grover A. Distribution patterns of hsp90 protein in rice. Plant Sci. 125:1997;221-230.
28. DeRocher A., Vierling E. Cytoplasmic hsp70 homologues of pea: differential expression vegetative and embryonic organs. Plant Mol. Biol. 27:1995;441-456.
29. DeRocher A.E., Vierling E. Developmental control of small heat shock protein expression during pea seed maturation. Plant J. 5:1994;93-102.
30. Krishna P., Reddy R.K., Sacco M., Frappier J.R.H., Felsheim R.F. Analysis of the native forms of the 90 kDa heat shock protein (hsp90) in plant cytosolic extracts. Plant Mol. Biol. 33:1997;457-466.
31. Kaukinen K.H., Tranbarger T.J., Misra S. Post-germination-induced and hormonally dependent expression of low-molecular-weight heat shock protein genes in Douglas fir. Plant Mol. Biol. 30:1996;1115-1128.
32. Kruse E., Liu Z., Kloppstech K. Expression of heat shock proteins during development of barley. Plant Mol. Biol. 23:1993;111-122.
33. Helm K.W., Abernethy R.H. Heat shock proteins and their mRNAs in dry and early imbibing embryos of wheat. Plant Physiol. 93:1990;1626-1633.