PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
12903118-2	2002	We introduced oligonucleotide containing a natural abasic site and a tetrahydrofuran abasic site into Rev1 mutants, rev1AA, which contains mutations of Asp467 and Glu468 residues of Rev1p to Ala in order to inactivate dCMP transferase activity, and rev1 delta, which lacks its whole coding sequence.	Oligonucleotides	14-29	deoxycytidyl transferase	Saccharomyces cerevisiae S288C	182-187	
12466536-9	2002	However, deletion of REV1 decreased the transformation efficiency with F-containing oligonucleotide as in the case of O.	Oligonucleotides	84-99	deoxycytidyl transferase	Saccharomyces cerevisiae S288C	21-25	
12903118-2	2002	We introduced oligonucleotide containing a natural abasic site and a tetrahydrofuran abasic site into Rev1 mutants, rev1AA, which contains mutations of Asp467 and Glu468 residues of Rev1p to Ala in order to inactivate dCMP transferase activity, and rev1 delta, which lacks its whole coding sequence.	Oligonucleotides	14-29	deoxycytidyl transferase	Saccharomyces cerevisiae S288C	116-120	
12903118-3	2002	The transformation efficiencies of rev1AA with abasic-containing oligonucleotides were lower than those of B7528, a strain proficient in REV1 gene, but much higher than rev1 delta mutant.	Oligonucleotides	65-81	deoxycytidyl transferase	Saccharomyces cerevisiae S288C	35-39