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嗜热四膜虫的表型分离率。

Rate of phenotypic assortment in Tetrahymena thermophila.

作者信息

Doerder F P, Deak J C, Lief J H

机构信息

Department of Biology, Cleveland State University, Ohio.

出版信息

Dev Genet. 1992;13(2):126-32. doi: 10.1002/dvg.1020130206.

Abstract

During vegetative, asexual reproduction in heterozygous Tetrahymena thermophila, the macronucleus divides amitotically to produce clonal lineages that express either one or the other allele but not both. Because such phenotypic assortment has been described for every locus studied, its mechanism has important implications concerning the development and structure of the macronucleus. The primary tools to study assortment are Rf, the rate at which subclones come to express a single allele stably, and the output ratio, the ratio of assortee classes. Because Rf is related to the number of assorting units, a constant Rf for all loci suggests that all genes are maintained at the same copy number. Output ratios reflect the input ratio of assorting units, with a 1:1 output ratio implying equal numbers of alleles at the end of macronuclear development. Because different outcomes would suggest a different macronuclear structure, it is crucial that these parameters be accurately measured. Although published Rf values are similar for all loci measured, there has been no commonly accepted form of presentation and analysis. Here we examine the experimental determination of Rf. First, we use computer simulation to describe how the variability inherent in the assortment process affects experimental determination of Rf. Second, we describe a simple method of plotting assortment data that permits the uniform calculation of Rf, and we describe how to measure Rf accurately in instances when it is possible to score only the recessive allele. Using this method to produce truly comparable Rfs for all published data, we find that most, if not all, loci assort at Rfs consistent with approximately 45 assorting units, as has been asserted.

摘要

在嗜热四膜虫杂合子进行无性营养繁殖期间,大核进行无丝分裂以产生克隆谱系,这些谱系表达其中一个或另一个等位基因,但不会同时表达两个等位基因。由于在所研究的每个基因座都描述了这种表型分离,其机制对于大核的发育和结构具有重要意义。研究分离的主要工具是Rf(亚克隆稳定表达单个等位基因的速率)和输出比率(分离类别的比率)。由于Rf与分离单位的数量有关,所有基因座的Rf恒定表明所有基因都保持相同的拷贝数。输出比率反映了分离单位的输入比率,1:1的输出比率意味着在大核发育结束时等位基因数量相等。由于不同的结果会表明大核结构不同,准确测量这些参数至关重要。尽管已发表的所有测量基因座的Rf值相似,但尚无普遍接受的呈现和分析形式。在这里,我们研究Rf的实验测定方法。首先,我们使用计算机模拟来描述分离过程中固有的变异性如何影响Rf的实验测定。其次,我们描述了一种绘制分离数据的简单方法,该方法允许统一计算Rf,并描述了在只能对隐性等位基因进行评分的情况下如何准确测量Rf。使用这种方法为所有已发表的数据生成真正可比的Rf,我们发现大多数(如果不是全部)基因座的Rf与大约45个分离单位一致,正如所断言的那样。

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