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JBC, Vol. 252, Issue 22, 8118-8125, Nov, 1977
G. I. Bell, L. J. DeGennaro, D. H. Gelfand, R. J. Bishop, P. Valenzuela and W. J. Rutter
The organization of the ribosomal DNA repeating unit from Saccharomyces
cerevisiae has been analyzed. A cloned ribosomal DNA repeating unit has
been mapped with the restriction enzymes Xma 1, Kpn 1, HindIII, Xba 1, Bgl
I + II, and EcoRI. The locations of the sequences which code for 5 S, 5.8
S, 18 S, and 25 S ribosomal RNAs have been determined by hybridization of
the purified RNA species with restriction endonuclease generated fragments
of the repeating unit. The position of the 5.8 S ribosomal DNA sequences
within the repeat was also established by sequencing the DNA which codes
for 83 nucleotides at the 5' end of 5.8 S ribosomal RNA. The polarity of
the 35 S ribosomal RNA precursor has been established by a combination of
hybridization analysis and DNA sequence determination and is 5'-18 S, 5.8
S, 25 S-3'.
Ribosomal RNA genes of Saccharomyces cerevisiae. I. Physical map of the repeating unit and location of the regions coding for 5 S, 5.8 S, 18 S, and 25 S ribosomal RNAs
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