1978
DOI: 10.1093/genetics/90.2.227
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MUTANTS OF SEXUAL MATURITY IN PARAMECIUM CAUDATUM SELECTED BY ERYTHROMYCIN RESISTANCE

Abstract: Cells of Paramecium caudatum, syngen 3 usually become sexually mature about 50 fissions after conjugation. In order to study the genetic mechanisms that control fission-dependent expression of maturity, an attempt was made to obtain early mature mutants by treatment with N-methyl-N′-nitro-N-nitro-soguanidine. A new cytoplasmic marker, erythromycin resistance, was used to eliminate nonconjugant and macronuclear regeneration clones. Twenty early mature clones were obtained from five different mutagenized culture… Show more

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Cited by 30 publications
(3 citation statements)
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“…Studies on sexual immaturity in P. multimicronucleatum, P. caudatum and P. bursaria, in which autogamy does not occur and thus there is no autogamy-immaturity, have shown that 1) its length is measured by some mechanism associated with the number of fissions (Kroll and Barnett, 1968;Miwa and Hiwatashi, 1970;Takagi, 1970), 2) its length is shortened by mytomicin (Miwa and Hiwatashi, 1970) or UV (Takagi, 1974) or codominant gene mutation (Myohara and Hiwatashi, 1978), 3) its length correlates with the length of the clonal life span (Smith- Sonneborn, 1981), 4) the transition from immaturity to maturity is stepwise and genetically controlled (Siegel, 1967;Takagi, 1988), and 5) immaturin, a protein of molecular weight 10,000 daltons, is responsible for maintaining the immature state (Haga and Hiwatashi, 1981;Miwa, 1984).…”
Section: Discussionmentioning
confidence: 99%
“…Studies on sexual immaturity in P. multimicronucleatum, P. caudatum and P. bursaria, in which autogamy does not occur and thus there is no autogamy-immaturity, have shown that 1) its length is measured by some mechanism associated with the number of fissions (Kroll and Barnett, 1968;Miwa and Hiwatashi, 1970;Takagi, 1970), 2) its length is shortened by mytomicin (Miwa and Hiwatashi, 1970) or UV (Takagi, 1974) or codominant gene mutation (Myohara and Hiwatashi, 1978), 3) its length correlates with the length of the clonal life span (Smith- Sonneborn, 1981), 4) the transition from immaturity to maturity is stepwise and genetically controlled (Siegel, 1967;Takagi, 1988), and 5) immaturin, a protein of molecular weight 10,000 daltons, is responsible for maintaining the immature state (Haga and Hiwatashi, 1981;Miwa, 1984).…”
Section: Discussionmentioning
confidence: 99%
“…Yt3 is a natural stock collected by Yuuji Tsukii. 27aG3 is an exautogamous clone derived from the early mature mutant clone Em IV-3S 27a established by Myohara & Hiwatashi (1978). Stock 16B205 is a CNR (non-reversal mutant) heterozygote produced by two back-crosses of 16B101 (cnrB/cnrB, Takahashi, 1979) to 27aG3.…”
Section: Materials and Methods (I) Stocks And Culture Methodsmentioning
confidence: 99%
“…In most species of ciliates, the length of the immaturity period is determined by the number of cell divisions after conjugation, and this number differs among species [ 3 , 4 , 5 , 6 ]. An analysis of a few mutants that have altered the length of immaturity provides compelling evidence that genetic factors influence the duration of the immature phase [ 7 , 8 , 9 ]. Sonneborn proposed the importance of immaturity based on population genetics; the presence of sexual immaturity provides time for offspring from the same mating to scatter around each other, preventing mating between closest relatives and avoiding inbreeding [ 3 ].…”
Section: Introductionmentioning
confidence: 99%