Skip to main content
Log in

Structural differences in full-length cDNAs for two classes of sporamin, the major soluble protein of sweet potato tuberous roots

  • Published:
Plant Molecular Biology Aims and scope Submit manuscript

Summary

Sporamin, which accounts for 80% of the total soluble proteins in sweet potato tuberous roots, consists of two polypeptide classes, A and B. The sporamin cDNA clones can also be classified into sporamin A and B subfamilies based on their sequence homologies, with intra-subfamily homologies being much higher than inter-subfamily homologies. The sequence of an essentially full-length cDNA for sporamin B was compared with that for sporamin A. The coding sequences of two cDNAs share 83% sequence homology. The sequences in the 5′- and 3′-noncoding regions show many deletions in addition to base substitutions. The endpoints of deletions longer than 4 bp match precisely to the endpoints of short direct repeats present in the other sequence, which suggests that these deletions are generated by slipped mispairing during DNA replication. In the 5′- and 3′-noncoding region of sporamin B cDNA, there are 5 bp direct repeats with sequences complementary to each other. Since most of these repeats are absent in sporamin A cDNA, these structural features may cause a difference in the secondary structure between A and B mRNAs and affect the translational efficiencies or stabilities of the mRNAs. Precursors for both classes of sporamin carry N-terminal extra-sequences which can be separated into a putative signal peptide segment and a segment enriched with basic amino acids. A two-step processing mechanism for the maturation of sporamin is suggested.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Crouch ML, Tenbarge KM, Simon AE, Ferl R: cDNA clones for Brassica napus seed storage proteins: Evidence from nucleotide sequence analysis that both subunits of napin are cleaved from a precursor polypeptide. J Mol Appl Genet 2:273–283, 1983.

    Google Scholar 

  2. Efstratiadis A, Posakony JW, Maniatis T, Lawn RM, O'Connell C, Sprits RA, DeRiel JK, Forget BG, Weissman SM, Slightom JL, Blechl AE, Smithies O, Baralle FE, Shoulders CC, Proudfoot NJ: The structure and evolution of the human β-globin gene family. Cell 21:653–668, 1980.

    Google Scholar 

  3. Farabaugh PJ, Miller JH: Genetic studies of the lac repressor: VII. On the molecular nature of spontaneous hotspots in the lacI gene of Escherichia coli. J Mol Biol 126:847–863, 1978.

    Google Scholar 

  4. Graham JS, Pearce G, Merryweather J, Titani K, Ericsson L, Ryan CA: Wound-induced proteinase inhibitors from tomato leaves; 1. The cDNA-deduced primary structure of pre-inhibitor 1 and its post-translational processing. J Biol Chem 260:6555–6560, 1985.

    Google Scholar 

  5. Grunstein M, Hogness D: Colony hybridization: A method for the isolation of cloned DNAs that contain specific gene. Proc Natl Acad Sci USA: 72:3961–3965, 1975.

    Google Scholar 

  6. Hall TC, Slightom JL, Ersland DR, Murray MG, Hoffman LM, Adang MJ, Brown JWS, Ma Y, Matthews JA, Cramer JH, Barker RF, Sutton DW, Kemp JD: Phaseolin: Nucleotide sequence explains molecular weight and charge heterogeneity of a small multigene family and also assists vector construction for gene expression in alien tissue. In: Ciferri O, DureIII L (eds) Structure and Function of Plant Genomes. Plenum Press, New York, 1983, pp 123–142.

    Google Scholar 

  7. Hattori T, Nakagawa T, Maeshima M, Nakamura K, Asahi T: Molecular cloning and nucleotide sequence of cDNA for sporamin, the major soluble protein of sweet potato tuberous roots. Plant Mol Biol 5:313–320, 1985.

    Google Scholar 

  8. Hattori T, Sakajo S, Iwasaki Y, Asahi T: Cell-free synthesis of succinate dehydrogenase and mitochondrial adenosine triphosphatase of sweet potato. Biochem Biophys Res Commun 113:235–240, 1982.

    Google Scholar 

  9. Kasarda DD, Okita TW, Bernardin JE, Baecker PA, Nimmo CC, Lew EJ-L, Dietler MD, Greene FC: Nucleic acid (cDNA) and amino acid sequences of α-type gliadins from wheat (Triticum aestivum). Proc Natl Acad Sci USA 81:4712–4716, 1984.

    Google Scholar 

  10. Maeshima M, Sasaki T, Asahi T: Characterization of major proteins in sweet potato tuberous roots. Phytochemistry 24:1899–1902, 1985.

    Google Scholar 

  11. Maniatis T, Fritsch EF, Sambrook J: Molecular Cloning. Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, 1982.

    Google Scholar 

  12. Messing J: New M13 vectors for cloning. Methods Enzymol 101:20–78, 1983.

    Google Scholar 

  13. Messing J, Geraghty D, Heidecker G, Hu N-T, Kridl J, Rubenstein I: Plant gene structure. In: Kosuge T, Meredith CP, Hollaender A (eds) Genetic Engineering of Plants. Plenum Press, New York, 1982, pp 211–227.

    Google Scholar 

  14. Mignery GA, Pikaard CS, Hannapel DJ, Park WD: Isolation and sequence analysis of cDNAs for the major potato tuber protein, patatin. Nucleic Acids Res 12:7987–8000, 1984.

    Google Scholar 

  15. Murray MG, Thompson WF: Rapid isolation of high molecular weight plant DNA. Nucl Acids Res 8:4321–4325, 1980.

    Google Scholar 

  16. Nakamura K, Hattori T, Asahi T: Direct immunological identification of full-length cDNA clones for plant protein without gene fusion to E. coli protein. FEBS Lett 198:16–20, 1986.

    Google Scholar 

  17. Nishiyama I: Evolution and domestication of the sweet potato. Bot Mag Tokyo 84:377–387, 1971.

    Google Scholar 

  18. Okayama H, Berg P: High-efficiency cloning of full-length cDNA. Mol Cell Biol 2:161–170, 1982.

    Google Scholar 

  19. Paiva E, Lister RM, Park WD: Induction and accumulation of major tuber proteins of potato in stems and petioles. Plant Physiol 71:161–168, 1983.

    Google Scholar 

  20. Perlman C, Halvorson HO: A putative signal peptidase recognition site and sequence in eukaryotic and prokaryotic signal peptides. J Mol Biol 167:391–409, 1983.

    Google Scholar 

  21. Rosahl S, Schmidt R, Schell J, Willmitzer L: Isolation and characterization of a gene from Solanum tuberosum encoding patatin, the major storage protein of potato tubers. Mol Gen Genet 203:214–220, 1986.

    Google Scholar 

  22. Salser H: Globin mRNA sequences: Analysis of base pairing and evolutionary implications. Cold Spring Harbor Symp Quant Biol 42:985–1002, 1977.

    Google Scholar 

  23. Schuler MA, Ladin BF, Pollaco JC, Freyer G, Beachy RN: Structural sequences are conserved in the genes coding for the α, α′ and β-subunits of soybean 7S storage protein. Nucl Acids Res 10:8245–8261, 1982.

    Google Scholar 

  24. Spena A, Krause E, Dobberstein B: Translation efficiency of zein mRNA is reduced by hybrid formation between the 5′- and 3′-untranslated region. EMBO J 4:2153–2158, 1985.

    Google Scholar 

  25. Zuker M, Stiegler P: Optimal computer folding of large RNA sequences using thermodynamics and auxiliary information. Nucl Acids Res 9:133–148, 1981.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Murakami, S., Hattori, T. & Nakamura, K. Structural differences in full-length cDNAs for two classes of sporamin, the major soluble protein of sweet potato tuberous roots. Plant Mol Biol 7, 343–355 (1986). https://doi.org/10.1007/BF00032564

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00032564

Keywords

Navigation