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Transcription of the gene encoding the 51 kd chlorophyll a-apoprotein of the photosystem II reaction centre from spinach

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Summary

Transcription of the plastid gene encoding the 51 kd chlorophyll a-conjugated polypeptide, which is presumed to carry the P680 reaction centre chlorophyll of photosystem II, has been studied both in vivo and in vitro in spinach. The gene is part of a polycistronic transcription unit whose expression involves both transcriptional and post-transcriptional regulation. Two distinct transcripts have been detected in RNA from chloroplasts as well as from etioplasts which start 55 and 175 nucleotides upstream of the protein-coding region. In vitro transcription of the gene in a homologous chloroplast extract yields only the “-175” terminus and only this 5′ end is preceded by typical prokaryotic promoter elements. The “-55” terminus lacks similar sequences but starts within a stem-loop structure. This suggests that the transcription initiation site of the gene is located 175 nucleotides upstream of the translational start codon and that the latter terminus is the result of post-transcriptional processing of the primary transcript. The start site for another transcription unit which is read in the opposite direction has been mapped 210 bp proximal to the “-175” terminus. The nature of its product is unknown. It is likely that the intergenic region contains all sequence elements necessary for the accurate transcription of both genes.

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References

  • Alt J, Westhoff P, Sears BB, Nelson N, Hurt E, Hauska G, Herrmann RG (1983) Genes and transcripts for the polypeptides of the cytochrome b6/f complex from spinach thylakoid membranes. EMBO J 2: 979–986

    Google Scholar 

  • Altman S, Guerrier-Takada C, Frankfort HM, Robertson HD (1982) RNA-processing nucleases. In: Linn SM, Roberts RJ (eds) Nucleases. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, pp 243–247

    Google Scholar 

  • Berk AJ, Sharp PA (1977) Sizing and mapping of early adenovirus mRNAs by gel electrophoresis of S1 endonuclease-digested hybrids. Cell 12: 721–732

    Google Scholar 

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

    Google Scholar 

  • Bohnert HJ, Crouse EJ, Schmitt JM (1982) Organization and expression of plastid genomes. In: Parthier B, Boulter D (eds) Encyclopedia of plant physiology, vol 14B. Springer Verlag, Berlin Heidelberg New York, pp 475–530

    Google Scholar 

  • Crossland LD, Rodermel SR, Bogorad L (1984) Single gene for the large subunit of ribulosebisphosphate carboxylase in maize yields two differentially regulated mRNAs. Proc Natl Acad Sci USA 81: 4060–4064

    Google Scholar 

  • Dente L, Cesareni G, Cortese R (1983) pEMBL: a new family of single stranded plasmids. Nucleic Acids Res 11: 1645–1655

    Google Scholar 

  • Erickson JM, Rahire M, Rochaix JD (1984) Chlamydomonas reinhardii gene for the 32,000 mol. wt. protein of photosystem II contains four large introns and is located entirely within the chloroplast inverted repeat. EMBO J 3: 2753–2762

    Google Scholar 

  • Greenberg BM, Gruissem W, Hallick RB (1984) Accurate processing and pseudouridylation of chloroplast transfer RNA in a chloroplast transcription system. Plant Mol Biol 3: 97–109

    Google Scholar 

  • Gruissem W, Greenberg BM, Zurawski G, Prescott DM, Hallick RB (1983) Biosynthesis of chloroplast transfer RNA in a spinach chloroplast transcription system. Cell 35: 815–828

    Google Scholar 

  • Hallick RB, Bottomley W (1983) Proposals for the naming of chloroplast genes. Plant Mol Biol Rep 1: 38–43

    Google Scholar 

  • Hanahan D (1983) Studies on transformation of Escherichia coli with plasmids. J Mol Biol 166: 557–580

    Google Scholar 

  • Heinemeyer W, Alt J, Herrmann RG (1984) Nucleotide sequence of the clustered genes for apocytochrome b6 and subunit 4 of the cytochrome b/f complex in the spinach plastid chromosome. Curr Genet 8: 543–549

    Google Scholar 

  • Hernandez N, Keller W (1983) Splicing of in vitro synthesized messenger RNA precursors in Hela cell extracts. Cell 35: 89–99

    Google Scholar 

  • Herrmann RG, Westhoff P, Alt J, Winter P, Tittgen J, Bisanz C, Sears BB, Nelson N, Hurt E, Hauska G, Viebrock A, Sebald W (1983) Identification and characterization of genes for polypeptides of the thylakoid membrane. In: Cifferi O, Dure L III (eds) Structure and function of plant genomes, vol 63. Life Sciences, pp 143–154

  • Herrmann RG, Westhoff P, Alt J, Tittgen J, Nelson N (1985) Thylakoid membrane proteins and their genes. In: van Vloten-Doting L, Groot GSP, Hall T (eds) Molecular form and function of the plant genome. Plenum Publishers, London, pp 233–256

    Google Scholar 

  • Krebbers ET, Larrinua IM, McIntosh L, Bogorad L (1982) The maize chloroplast genes for the β and, ε subunits of photosynthetic coupling factor CF1 are fused. Nucleic Acids Res 10: 4985–5002

    Google Scholar 

  • Link G (1984) DNA sequence requirements for the accurate transcription of a protein-coding plastid gene in a plastid in vitro system from mustard (Sinapis alba L). EMBO J 3: 1697–1704

    Google Scholar 

  • Maniatis T, Fritsch EF, Sambrook J (1982) Molecular cloning. Cold Spring Harbor Laboratory, NY

    Google Scholar 

  • Maxam AM, Gilbert W (1980) Sequencing end-labelled DNA with base-specific chemical cleavages. Methods Enzymol 65: 499–560

    Google Scholar 

  • McMaster GK, Carmichael GG (1977) Analysis of single- and double-stranded nucleic acids in polyacrylamide and agarose gels by using glyoxal and acridine orange. Proc Natl Acad Sci USA 74: 4835–4838

    Google Scholar 

  • Messing J, Gronenborn B, Müller-Hill B, Hofschneider PH (1977) Filamentous coliphage M13 as a cloning vehicle in insertion of a HindIII fragment of the lac regulatory region in M13 replicative form in vitro. Proc Natl Acad Sci USA 74: 3642–3646

    Google Scholar 

  • Morris J, Herrmann RG (1984) Nucleotide sequence of the gene for the P680 chlorophyll a apoprotein of the photosystem II reaction center from spinach. Nucleic Acids Res 6: 2837–2850

    Google Scholar 

  • Mullet JE, Orozco EM, Chua NH (1985) Multiple transcripts for higher plant rbcL and atpB genes and localization of the transcription initiation site of the rbcL gene. Plant Mol Biol 4: 39–54

    Google Scholar 

  • Nakatani HY, Ke B, Dolan E, Arntzen CJ (1984) Identity of the photosystem II reaction center polypeptide. Biochem Biophys Acta 765: 347–352

    Google Scholar 

  • Padgett RA, Hardy SF, Sharp PA (1983) Splicing of adenovirus RNA in a cell-free transcription system. Proc Natl Acad Sci USA 80: 5230–5234

    Google Scholar 

  • Parthier B (1982) The cooperation of nuclear and plastid genomes in plastid biogenesis and differentiation. Biochem Physiol Pflanzen 177: 283–317

    Google Scholar 

  • Pelham HRB, Jackson RJ (1976) An efficient mRNA-dependent translation system from reticulocyte lysates. Eur J Biochem 67: 247–256

    Google Scholar 

  • Poulsen C (1984) Two mRNA species differing by 258 nucleotides at the 5′ end are formed from the barley chloroplast rbcL gene. Carlsberg Res Commun 49: 89–104

    Google Scholar 

  • Rosenberg M, Court D (1979) Regulatory sequences involved in the promotion and termination of RNA transcription. Annu Rev Genet 13: 319–353

    Google Scholar 

  • Rüther U (1982) pUR250 allows rapid chemical sequencing of both DNA strands of its inserts. Nucleic Acids Res 10: 5765–5762

    Google Scholar 

  • Shinozaki K, Sugiura M (1982) Sequence of the intercistronic region between the ribulose-1,5-bisphospate carboxylase/oxygenase large subunit and the coupling factor beta subunit gene. Nucleic Acids Res 10: 4923–4934

    Google Scholar 

  • Strub K, Galli G, Busslinger M, Birnstiel ML (1984) The cDNA sequences of the sea urchin U7 small nuclear RNA suggest specific contacts between histone mRNA precursor and U7 RNA during RNA processing. EMBO J 3: 2801–2807

    Google Scholar 

  • Thomas PS (1980) Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose. Proc Natl Acad Sci USA 77: 5201–5205

    Google Scholar 

  • Weaver RF, Weissmann C (1979) Mapping of RNA by a modification of the Berk-Sharp procedure: the 5′ termini of 15S β-globin mRNA precursor and mature 10S β-globin mRNA have identical map coordinates. Nucleic Acids Res 7: 1175–1193

    Google Scholar 

  • Westhoff P, Alt J, Herrmann RG (1983) Localization of the genes for the two chlorophyll a-conjugated polypeptides (mol. wt. 51 and 44 kd) of the photosystem II reaction center on the spinach plastid chromosome. EMBO J 2: 2229–2237

    Google Scholar 

  • Westhoff P, Nelson N, Bünemann H, Herrmann RG (1981) Localization of genes for coupling factor subunits on the spinach plastid chromosome. Curr Genet 4: 109–120

    Google Scholar 

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Communicated by C.P. Hollenberg

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Westhoff, P. Transcription of the gene encoding the 51 kd chlorophyll a-apoprotein of the photosystem II reaction centre from spinach. Molec. Gen. Genet. 201, 115–123 (1985). https://doi.org/10.1007/BF00397995

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