By F. Ehrendorfer (auth.), Prof. Dr. U. Jensen, Prof. Dr. D. E. Fairbrothers (eds.)
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Extra info for Proteins and Nucleic Acids in Plant Systematics
Ulmer, Stuttgart Nagl W (1982) In: Parthier B, Bouher D (eds) Nuc1eic acids in plants 11. Encycl Plant Physiol, vo114B. Springer, Berlin Heidelberg New York, pp 1-45 Nagl W, Ehrendorfer F (1974) Plant Syst EvoI123:35-54 Nagl W, Capesius I (1976) Plant Syst EvolI26:221-237 Nagl W, Capesius I (1977) Chromosomes Today 6:141-150 Nagl W, Hernieben V, Ehrendorfer F (eds) (1979) Genomeand chromatin: Organization, evolution, function. Symp Kaiserslautern. Plant Syst Evol Suppl 2 Nagl W, Fusenig HP (1979) Plant Syst Evol Suppl2: 221-233 Nagl W, Bachmann K (1980) Theor Appl Genet 57:107-111 34 F.
G. the entire BamHI fragments: 3,000 bp in mustard, 3,200 pb in maize, or the large BglII fragments: 2,200 bp in mustard, 2,220 bp in maize). Another reason is of course a relatively low sampling number - Le. number offragments compared - even ifmanymore restriction enzymes than in Figs_ 2 and 3 had been used. Finally, the percentage of conserved restriction sites - even if the sampling were of sufficient size - would reflect the actual sequence homology in an unknown and probably nonlinear way.
Probe 1 was derived from a subclone; besides the leader rDNA it contained pBR322 vector sequences (Zenke and Kössel unpublished) which lead to the strong band in the upper region of the autoradiographic picture (cross hybridization of vector DNA); only the lower weak band corresponding to the mustard fragment HincII/HindIII. G600 is due to chloroplast DNA cross hybridization as is the case for all autoradiographic bands of the other pictures. In C the fragments of mustard chloroplastrDNAhybridizing with the maize rDNA prob es are summarized in correlation to the mustard rDNA map (0).