Skip to main content
Log in

Isolation and characterization of cDNA clones corresponding with mRNAs that accumulate during auxin-induced lateral root formation

  • Published:
Plant Molecular Biology Aims and scope Submit manuscript

Abstract

Lateral root formation in root cultures of Arabidopsis thaliana can be initiated by exogenous addition of auxin. In order to find cDNA clones of which the corresponding mRNAs accumulate during this process, a cDNA library was constructed from root cultures treated with the active auxin 1-naphthaleneacetic acid (1- NAA). Differential screening of this library with cDNA probes derived from mRNA populations isolated from root cultures treated with 1-NAA and the inactive analogue 2-naphthaleneacetic acid (2-NAA) led to the isolation of four cDNA clones, designated AIR1, AIR3, AIR9 and AIR12. Accumulation of the mRNAs starts between 4 and 8 h and continues till at least 24 h after addition of an active auxin. Sequence analysis revealed that AIR1 encodes a protein that is related to a large family of proteins that consist of a proline-rich or glycine- rich N-terminus and a hydrophobic, possibly membrane spanning C- terminus. The putative function of these proteins is coupling of the cell wall to the plasma membrane. Surprisingly, AIR1 lacks the proline-rich or glycine-rich N-terminus which is thought to be important for interaction with the cell wall. AIR3 encodes a subtilisin-like serine protease which is believed to be active outside the plant cell. Although AIR9 and AIR12 do not show any significant homology to sequences in the database, they are also predicted to function outside the cell. Our screening thus indicates that a variety of genes encoding extracellular proteins are activated during auxin-induced lateral root formation.

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. Ahn JH, Choi Y, Kwon YM, Kim SG, Choi YD, Lee JS: A novel extensin gene encoding a hydroxyproline-rich glycoprotein requires sucrose for its wound-inducible expression in transgenic plants. Plant Cell 8: 1477–1490 (1996).

    Google Scholar 

  2. Aleith F, Richter G: Gene expression during induction of somatic embryogenesis in carrot cell suspensions. Planta 183: 17–24 (1990).

    Google Scholar 

  3. Bánfalvi Z, Molnár A, Molnár G, Lakatos L, Szabó L: Starch synthesis-, and tuber storage protein genes are differently expressed in Solanum tuberosum and in Solanum brevidens. FEBS Lett 383: 159–164 (1996).

    Google Scholar 

  4. Barr PJ: Mammalian subtilisins: the long-sought dibasic processing endoproteases. Cell 66: 1–3 (1991).

    Google Scholar 

  5. Baud F, Pebay-Peyroula E, Cohen-Addad C, Odani S, Lehmann MS: Crystal structure of hydrophobic protein from soybean; a member of a new cysteine-rich family. J Mol Biol 231: 877–887 (1993).

    Google Scholar 

  6. Birnboim HC, Doly J: A rapid alkaline extraction procedure for screening recombinant plasmid DNA. Nucl Acids Res 7: 1513–1523 (1979).

    Google Scholar 

  7. Blakely LM, Blakely RM, Colowit PM, Elliott DS: Experimental studies on lateral root formation in radish seedling roots. II. Analysis of the dose-response to exogenous auxin. Plant Physiol 87: 414–419 (1988).

    Google Scholar 

  8. Callis J, Carpenter T, Sun CW, Vierstra RD: Structure and evolution of genes encoding polyubiquitin and ubiquitin-like proteins in Arabidopsis thaliana ecotype Columbia. Genetics 139: 921–939 (1995).

    Google Scholar 

  9. Cassab GI, Varner JE: Cell wall proteins. Annu Rev Plant Physiol Plant Mol Biol 39: 321–353 (1988).

    Google Scholar 

  10. Castonguay Y, Laberge S, Nadeau P, Vézina LP: A coldinduced gene from Medicago sativa encodes a bimodular protein similar to developmentally regulated proteins. Plant Mol Biol 24: 799–804 (1994).

    Google Scholar 

  11. Celenza JL Jr., Grisafi PL, Fink GR: A pathway for lateral root formation in Arabidopsis thaliana. Genes Dev 9: 2131–2142 (1995).

    Google Scholar 

  12. Choi DW, Song JY, Kwon YM, Kim SG: Characterization of a cDNA encoding a proline-rich 14 kDa protein in developing cortical cells of the roots of bean (Phaseolus vulgaris) seedlings. Plant Mol Biol 30: 973–982 (1996).

    Google Scholar 

  13. Coupe SA, Taylor JE, Isaac PG, Roberts JA: Identification and characterization of a proline-rich mRNA that accumulates during pod development in oilseed rape (Brassica napus L.). Plant Mol Biol 23: 1223–1232 (1993).

    Google Scholar 

  14. Czakó M, Wilson J, Yu X, Márton L: Sustained root culture for generation and vegetative propagation of transgenic Arabidopsis thaliana. Plant Cell Rep 12: 603–606 (1993).

    Google Scholar 

  15. Datta N, LaFayette PR, Kroner PA, Nagao PT, Key JL: Isolation and characterization of three families of auxin downregulated cDNA clones. Plant Mol Biol 21: 859–869 (1993).

    Google Scholar 

  16. Davies PJ: Plant Hormones and their Role in Plant Growth and Development. Kluwer Academic Publishers, Dordrecht, Netherlands (1996).

    Google Scholar 

  17. Deutch CE, Winicov I: Post-transcriptional regulation of a salt-inducible alfalfa gene encoding a putative chimeric proline-rich cell wall protein. Plant Mol Biol 27: 411–418 (1995).

    Google Scholar 

  18. Devereux J, Haeberli P, Smithies O: A comprehensive set of sequence analysis programs for the VAX. Nucl Acids Res 12: 387–395 (1984).

    Google Scholar 

  19. Doerner P, Jørgensen JE, You R, Steppuhn J, Lamb C: Control of root growth and development by cyclin expression. Nature 380: 520–523 (1996).

    Google Scholar 

  20. Dolan L, Janmaat K, Willemsen V, Linstead P, Poethig S, Roberts K, Scheres B: Cellular organization of the Arabidopsis thaliana root. Development 119: 71–84 (1993).

    Google Scholar 

  21. Feinberg AP, Vogelstein B: A technique for radiolabelling restriction endonuclease fragments to high specific activity. Anal Biochem 132: 6–13 (1983).

    Google Scholar 

  22. Ferreira PC, Hemerly AS, Engler JD, Van Montagu M, Engler G, lnzé D: Developmental expression of the Arabidopsis cyclin gene cyclAt. Plant Cell 6: 1763–1774 (1994).

    Google Scholar 

  23. Fujita T, Kouchi H, Takanari I, Sy¯ono K: Cloning of cDNAs for genes that are specifically or preferentially expressed during the development of tobacco genetic tumors. Plant J 5: 645–654 (1997).

    Google Scholar 

  24. Goodwin W, Pallas JA, Jenkins GI: Transcripts of a gene encoding a putative cell wall-plasma membrane linker protein are specifically cold-induced in Brassica napus. Plant Mol Biol 31: 771–781 (1996).

    Google Scholar 

  25. Hotze M, Waitz A, Schröder J: cDNA for a 14-kilodalton polypeptide from Madagascar periwinkle (Catharanthus roseus). Plant Physiol 104: 1097–1098 (1994).

    Google Scholar 

  26. John I, Wang H, Held BM, Syrkin Wurtele E, Colbert JT: An mRNA that specifically accumulates in maize roots delineates a novel subset of developing cortical cells. Plant Mol Biol 20: 821–831 (1992).

    Google Scholar 

  27. Josè-Estanyol M, Ruiz-Avila L, Puigdomènech P: A maize embryo-specific gene encodes a proline-rich and hydrophobic protein. Plant Cell 4: 413–423 (1992).

    Google Scholar 

  28. Joshi CP: Putative polyadenylation signals in nuclear genes of higher plants: a compilation and analysis. Nucl Acids Res 15: 9627–9640 (1987).

    Google Scholar 

  29. Kaneda M, Tominaga N: Isolation and characterization of a protease from the sarcocarp of melon fruit. J Biochem 78: 1287–1296 (1975).

    Google Scholar 

  30. Keller B, Lamb CJ: Specific expression of a novel cell wall hydroxyproline-rich glycoprotein gene in lateral root initiation. Genes Dev 3: 1639–1646 (1989).

    Google Scholar 

  31. Kieliszewski MJ, Lamport DT: Extensin: repetitive motifs, functional sites, post-translational codes, and phylogeny. Plant J 5: 157–172 (1994).

    Google Scholar 

  32. King GA, O'Donoghue EM, Borst WM, Davies KM, Moyle RL, Farnden KJ: Identification and characterization of an mRNA encoding a proline-rich protein that rapidly declines in abundance in the tips of harvested asparagus spears. Plant Cell Physiol 37: 706–710 (1996).

    Google Scholar 

  33. Kobayashi T, Kobayashi E, Sato S, Hotta Y, Miyajima N, Tanaka A, Tabata S: Characterization of cDNAs induced in meiotic prophase in lily microsporocytes. DNA Res 1: 15–26 (1994).

    Google Scholar 

  34. Malamy JE, Benfey PN: Organization and cell differentiation in lateral roots of Arabidopsis thaliana. Development 124: 33–44 (1997).

    Google Scholar 

  35. Martinez MC, Jørgensen JE, Lawton MA, Lamb CJ, Doerner PW: Spatial pattern of cdc2 expression in relation to meristem activity and cell proliferation during plant development. Proc Natl Acad Sci USA 89: 7360–7364 (1992).

    Google Scholar 

  36. McGurl B, Pearce G, Orozco-Cardenas M, Ryan CA: Structure, expression, and antisense inhibition of the systemin precursor gene. Science 255: 1570–1573 (1992).

    Google Scholar 

  37. Murashige T, Skoog F: A revised medium for rapid growth and bioassays with tobacco tissue culture. Physiol Plant 15: 473–497 (1962).

    Google Scholar 

  38. Nielsen H, Engelbrecht J, Brunak S, von Heijne G: Identification of prokaryotic and eukaryotic signal peptides and prediction of their cleavage sites. Protein Eng 10: 1–6 (1997).

    Google Scholar 

  39. Nishida T, Ohnishi N, Kodama H, Komamine A: Establishment of synchrony by starvation and readdition of auxin in suspension cultures of Catharanthus roseus cells. Plant Cell Tissue Organ Cult 28: 37–43 (1992).

    Google Scholar 

  40. Odani S, Koide T, Ono T, Seto Y, Tanaka T: Soybean hydrophobic protein. Isolation, partial characterization and the complete primary structure. Eur J Biochem 162: 485–491 (1987).

    Google Scholar 

  41. Ribeiro A, Akkermans AD, van Kammen A, Bisseling T, Pawlowski K: A nodule-specific gene encoding a subtilisinlike protease is expressed in early stages of actinorhizal nodule development. Plant Cell 7: 785–794 (1995).

    Google Scholar 

  42. Richards KD, Gardner RC: pEARLI1: an Arabidopsis member of a conserved gene family. Plant Physiol 109: 1497 (1995).

    Google Scholar 

  43. Romano CP, Robson PR, Smith H, Estelle M, Klee H: Transgene-mediated auxin overproduction in Arabidopsis: hypocotyl elongation phenotype and interactions with the hy6–1 hypocotyl elongation and axr1 auxin-resistant mutants. Plant Mol Biol 27: 1071–1083 (1995).

    Google Scholar 

  44. Rudenskaya GN, Bogdanova EA, Revina LP, Golovkin BN, Stepanov VM: Macluralisin a serine proteinase from fruits of Maclura pomifera (Raf.) Schneid. Planta 196: 174–179 (1995).

    Google Scholar 

  45. Ruegger M, Dewey E, Hobbie L, Brown D, Bernasconi P, Turner J, Muday G, Estelle M: Reduced naphthylphthalamic acid binding in the tir3 mutant of Arabidopsis is associated with a reduction in polar auxin transport and diverse morphological defects. Plant Cell 9: 745–757 (1997).

    Google Scholar 

  46. Sabala I, Franzén H, von Arnold S: A spruce gene, af70, constitutively expressed in somatic embryos and induced by ABA and low temperature in seedlings. Physiol Plant 99: 316–322 (1997).

    Google Scholar 

  47. Sakuma Y, Azuma T, Kato Y, Kojima Y, Miura K: Cytokinininduced mRNA in the suspension cultured cell of poplar (Populus nigra). Mokuzai Gakkaishi 42: 789–794 (1996).

    Google Scholar 

  48. Salts Y, Wachs R, Gruissem W, Barg R: Sequence coding for a novel proline-rich protein preferentially expressed in young tomato fruit. Plant Mol Biol 17: 149–150 (1991).

    Google Scholar 

  49. Sambrook L, Fritsch EF, Maniatis T: Molecular Cloning: A Laboratory Manual, 2nd ed. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY (1989).

    Google Scholar 

  50. Sanger F, Nicklen S, Coulson AR: DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci USA 74: 5463–5467 (1977).

    Google Scholar 

  51. Santino CG, Stanford GL, Conner TW: Developmental and transgenic analysis of two tomato fruit enhanced genes. Plant Mol Biol 33: 405–416 (1997).

    Google Scholar 

  52. Schaller A, Ryan CA: Identification of a 50-kDa systemin binding protein in tomato plasma membranes having Kex2plike properties. Proc Natl Acad Sci USA 91: 11802–11806 (1994).

    Google Scholar 

  53. Schuurink RC: Molecular and ultrastructural studies of the aleurone layer in dormant and non-dormant barley grains. Ph.D. thesis, University of Leiden, Netherlands (1993).

    Google Scholar 

  54. Showalter AM: Structure and function of plant cell wall proteins. Plant Cell 5: 9–23 (1993).

    Google Scholar 

  55. Siezen RJ, de Vos WM, Leunissen JA, Dijkstra BW: Homology modelling and protein engineering strategy of subtilases, the family of subtilisin-like serine proteinases. Protein Eng 4: 719–737 (1991).

    Google Scholar 

  56. Silen JL, Agard DA: The alpha-lytic protease pro-region does not require a physical linkage to activate the protease domain in vivo. Nature 341: 462–464 (1989).

    Google Scholar 

  57. Subramaniam K, Ranie J, Srinivasa BR, Sinha AM, Mahadevan S: Cloning and sequence of a cDNA encoding a novel hybrid proline-rich protein associated with cytokinin-induced haustoria formation in Cuscuta reflexa. Gene 141: 207–210 (1994).

    Google Scholar 

  58. Taylor BH, Scheuring CF: A molecular marker for lateral root initiation: the RSI-1 gene of tomato (Lycopersicon esculentum Mill) is activated in early lateral root primordia. Mol Gen Genet 243: 148–157 (1994).

    Google Scholar 

  59. Taylor BH, Young RJ, Scheuring CF: Induction of a proteinase inhibitor II-class gene by auxin in tomato roots. PlantMol Biol 23: 1005–1014 (1993).

    Google Scholar 

  60. Taylor AA, Horsch A, Rzepczyk A, Hasenkampf CA, Riggs CD: Maturation and secretion of a serine proteinase is associated with events of late microsporogenesis. Plant J 12: 1261–1271 (1997).

    Google Scholar 

  61. Tornero P, Conejero V, Vera P: Primary structure and expression of a pathogen-induced protease (PR-P69) in tomato plants: similarity of functional domains to subtilisin-like endoproteases. Proc Natl Acad Sci USA 93: 6332–6337 (1996).

    Google Scholar 

  62. Tornero P, Conejero V, Vera P: Identification of a new pathogen-induced member of the subtilisin-like processing protease family from plants. J Biol Chem 272: 14412–14419 (1997).

    Google Scholar 

  63. Torrey JG: The induction of lateral roots by indoleacetic acid and root decapitation. Am J Bot 37: 257–264 (1950).

    Google Scholar 

  64. van de Sande K, Pawlowski K, Czaja I, Wieneke U, Schell J, Schmidt J, Walden R, Matvienko M, Wellink J, van Kammen A, Franssen H, Bisseling T: Modification of phytohormone response by a peptide encoded by EN0D40 of legumes and a nonlegume. Science 273: 370–373 (1996).

    Google Scholar 

  65. van der Zaal EJ, Memelink J, Mennes AM, Quint A, Libbenga KR: Auxin-induced mRNA species in tobacco cell cultures. Plant Mol Biol 10: 145–157 (1987).

    Google Scholar 

  66. van Slogteren GMS, Hoge JHC, Hooykaas PJJ, Schilperoort RA: Clonal analysis of heterogenous crown gall tumor tissues induced by wildtype and shooter mutant strains of Agrobacterium tumefaciens: expression of T-DNA genes. Plant Mol Biol 2: 321–333 (1983).

    Google Scholar 

  67. Vera P, Lamb C, Doerner PW: Cell-cycle regulation of hydroxyproline-rich glycoprotein HRGPnt3 gene expression during the initiation of lateral root meristems. Plant J 6: 717–727 (1994).

    Google Scholar 

  68. Winicov I, Deutch CE: Characterization of a cDNA clone from salt-tolerant alfalfa cells that identifies salt-inducible root-specific transcripts. J Plant Physiol 144: 222–228 (1994).

    Google Scholar 

  69. Xu Y, Buchholz WG, DeRose RT, Hall TC: Characterization of a rice gene family encoding root-specific proteins. Plant Mol Biol 27: 237–248 (1995).

    Google Scholar 

  70. Yaish SA: Ph.D thesis, University of Durham (1990).

  71. Yamagata H, Masuzawa T, Nagaoka Y, Ohnishi T, Iwasaki T: Cucumisin, a serine protease from melon fruits, shares structural homology with subtilisin and is generated from a large precursor. J Biol Chem 269: 32725–32731 (1994).

    Google Scholar 

  72. Yasuda E, Ebinuma H, Wabiko H: A novel glycinerich/ hydrophobic 16 kDa polypeptide gene from tobacco: similarity to proline-rich protein genes and its wound-inducible and developmentally regulated expression. Plant Mol Biol 33: 667–678 (1997).

    Google Scholar 

  73. Zhu XL, Ohta Y, Jordan F, Inouye M: Pro-sequence of subtilisin can guide the refolding of denatured subtilisin in an intramolecular process. Nature 339: 483–484 (1989).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Neuteboom, L.W., Ng, J.M., Kuyper, M. et al. Isolation and characterization of cDNA clones corresponding with mRNAs that accumulate during auxin-induced lateral root formation. Plant Mol Biol 39, 273–287 (1999). https://doi.org/10.1023/A:1006104205959

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1006104205959

Navigation