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Nuclei from sea urchin blastula embryos synthesize a variety of small RNAs, one of which has identical mobility with sea urchin U1 RNA. This RNA is synthesized by RNA polymerase II and, in a hybridization-selection experiment, was selected by the cloned sea urchin U1 gene. The U1 RNA was initiated with ATP, but not GTP, in isolated nuclei with beta-S- and gamma-S-ribonucleotide triphosphates as substrates. The U1 RNA containing thiophosphate at the 5'' end was not capped but accumulated as an uncapped transcript from which the thiophosphate could be removed with calf intestinal phosphatase.
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The terminal RNA stem-loop structure and 80 bp of spacer DNA are required for the formation of 3' termini of sea urchin H2A mRNA.
1983, Pubmed,
Echinobase
Birchmeier,
The terminal RNA stem-loop structure and 80 bp of spacer DNA are required for the formation of 3' termini of sea urchin H2A mRNA.
1983,
Pubmed
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Echinobase
Blin,
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Pubmed
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Echinobase
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1980,
Pubmed
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1985,
Pubmed
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Echinobase
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Pubmed
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Pubmed
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1982,
Pubmed
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Echinobase
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Echinobase
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Pubmed
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1984,
Pubmed
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1979,
Pubmed
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1980,
Pubmed
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Cloning and organization of genes for 5S ribosomal RNA in the sea urchin. Lytechinus variegatus.
1981,
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Echinobase
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Pubmed
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Pubmed
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Echinobase
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1983,
Pubmed
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Pubmed
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Echinobase
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Pubmed
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Pubmed
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Pubmed
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Pubmed