MUTANTS OF PARAMECIUM DEFECTIVE IN CHEMOKINESIS TO FOLATE
Author(s) -
Mary C DiNallo,
Mark E. Wohlford,
Judith Van Houten
Publication year - 1982
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1093/genetics/102.2.149
Subject(s) - complementation , mutant , biology , paramecium , genetics , mendelian inheritance , phenotype , allele , gene , mutation , mutagenesis , microbiology and biotechnology
Ten mutant lines of Paramecium tetraurelia defective in attraction to folate were isolated and examined. All mutants were normal in response to other attractants and repellents tested. One mutant was able to accumulate in folate given sufficient time. All mutations were recessive and behaved as single site Mendelian lesions. Complementation tests indicate that the mutants fall into three complementation groups. Mutants of Group 2 fall into two phenotypic classes and probably represent two alleles of the mutated fol2 gene. Possible sites of the mutants' blocks in chemoresponse are discussed.
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