Handbook of Plant and Crop Physiology

(Steven Felgate) #1

  1. G Haberhausen, K Zetsche. Functional loss of all ndhgenes in an otherwise relatively unaltered plastid genome
    of the holoparasitic plant Cuscuta reflexa. Plant Mol Biol 24:217–222, 1994.

  2. MA Machado, K Zetshe. A structural, functional and molecular analysis of plastids of the holoparasites Cus-
    cuta reflexaandCuscuta europaea. Planta 181:91–96, 1990.

  3. AD Wolfe, CW Morden, JD Palmer. Function and evolution of a minimal plastid genome from a non-photo-
    synthetic parasitic plant. Proc Natl Acad Sci U S A 98:10648–10652, 1992.

  4. P Thalouarn, S Renaudin. Polymerase chain reaction evidence of the rbsL gene in the Scrophulariaceae
    holoparasiteLathrea cladestinaL. Comparison with the autotroph Digitalis purpureaL. and hemiparasite
    Melampyrum pratenzeL. C R Acad Sci Paris 309:381–387, 1991.

  5. CF Wimpee, R Morgan, RL Wrobel. An aberrant plastid ribosomal RNA gene cluster in the root parasite
    Conopholis americana. Plant Mol Biol 18:275–285, 1992.

  6. CF Wimpee, R Morgan, RL Wrobel. Loss of transfer RNA genes from the plastid 16S–23S ribosomal RNA
    gene spacer in a parasitic plant. Curr Genet 21:417–422, 1992.

  7. P Thalouarn, C Theodet, N Russo, P Delavault. The reduced plastid genome of a nonphotosynthetic an-
    giospermOrobanche hederaehas retained the rbsL gene. Plant Physiol Biochem 32:233–242, 1994.

  8. AD Wolfe, CW dePamphillis. Alternate paths of evolution for the photosynthetic gene rbcL in four nonphoto-
    synthetic species of Orobanche. Plant Mol Biol 33:965–977, 1997.

  9. AD Wolfe, CW dePamphillis. The effect of relaxed functional constraints on the photosynthetic gene rbcL in
    photosynthetic and nonphotosynthetic parasitic plants. Mol Biol Evol 15:1243–1258, 1998.

  10. P Westhoff. The genetic material of plant cells is compartmentalized: structure and expression of the
    subgenomes. In: P Westhoff, H Jeske, G Jurgens, K Kloppstech, G Link, eds. Molecular Plant Development,
    from Gene to Plant. Oxford: Oxford University Press, 1998, pp 67–109.

  11. MR Hanson, O Folkerts. Structure and function of the higher plant mitochondrial genome. Int Rev Cytol
    141:129–172, 1992.

  12. W Schuster, A Brennicke. The plant mitochondrial genome: physical structure, information content, RNA edit-
    ing, and gene migration to the nucleus. Annu Rev Plant Physiol 45:61–78, 1994.

  13. C Dean, R Schmidt. Plant genomes: a current molecular description. Annu Rev Plant Physiol 46:395–418,



  14. R Bock, H Koop. Extraplastidic site-specific factors mediate RNA editing in chloroplasts. EMBO
    16:3282–3288, 1997.

  15. R Bock. Analysis of RNA editing. In: Plastids Methods: A Companion to Methods Enzymol 15:75–83, 1998.

  16. TM Clegg, MP Cummings, ML Durbin. The evolution of plant nuclear genes. Proc Natl Acad Sci U S A
    94:7791–7798, 1997.

  17. A Hirai, M Nakasono. Six percent of the mitochondrial genome of race came from chloroplast DNA. Plant Mol
    Biol Rep 11:98–100, 1993.

  18. MW Gray. The endosymbiont hypothesis revised. Int Rev Cytol 141:233–358, 1992.

  19. J Doebly. Genetics, development and plant evolution. Curr Opin Genet Dev 3:865–872, 1993.

  20. G Moore. Cereal genome evolution: pastoral pursuits with “Lego” genomes. Curr Opin Genet Dev 5:717–724,



  21. PE Thorsness, ER Weber. Escape and migration of nucleic acids between chloroplasts, mitochondria and the
    nucleus. Int Rev Cytol 165:207–234, 1996.

  22. M Sugita, M Sugiura. Regulation of gene expression in chloroplast of higher plants. Int Rev Cytol 32:315–326,



  23. S Binder, A Marchfelder, A Brennicke. Regulation of gene expression in plant mitochondria. Plant Mol Biol
    32:303–314, 1996.

  24. M Goldschmidt-Clermont. Coordination of nuclear and chloroplast gene expression in plant cells. Int Rev Cy-
    tol 177:115–180, 1998.

  25. MW Gray. Origin and evolution of organelle genomes. Curr Opin Genet Dev 3:884–890, 1993.

  26. M Singh, PS Krishnan. Isolation of mitochondria from Orobanche, a “total” root angiospermic parasite. Phys-
    iol Plant 39(2):179–184, 1977.

  27. M Singh, PS Krishnan. Enzymatic activity in mitochondria from Orobanche. Physiol Plant 40(2):145–152,



  28. A Ljubenova. Comparative investigation of genotypes from genus Orobanche—broomrape using DNA molec-
    ular markers. PhD thesis, Plovdiv, Bulgaria, 1999.


PARASITIC FLOWERING PLANTS OF GENUS OROBANCHE 801

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