PubMed HealthSearch

PubMed · 338129

Recombination values and their errors.

Abstract

Two four-point testcrosses comprising 87,000 tomato plants were grown and the data collected from 28 subgroups. Each subgroup consisted of 2,000 or 5,000 plants and should give a valid estimate of the three recombination values. The 28 values for each interval give more outlyers (23% are outside the 95% limits set by the standard deviation calculated by the binomial formula square root of p q/n) than would be expected by chance. If each subgroup was regarded as the control and the other groups tested against this, then 42% of the time the two subgroups would be significantly different. It is suggested that there are many cases in the literature where this comparison has been made and the significant difference wrongly ascribed to treatment. While the causes of these changes in recombination value are unknown and therefore uncontrollable, they must be anticipated in all such studies. Control and treatment must be replicated enough that chance extreme values will not be attributed to treatment.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

L Butler. 1977. Recombination values and their errors.. https://doi.org/10.1139/g77-055

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Functional analysis of the homeodomain-related proteins of the A alpha locus of Schizophyllum commune.

DNA-mediated transformation was used to correlate function with putative genes from three alternative A alpha mating-type loci (A alpha 1, A alpha 3, and A alpha 4) of Schizophyllum commune. Each DNA was tested in at least nine haploid strains, one for each of the nine A alpha mating types found in the world-wide population of S. commune. The Y and Z genes (tentatively identified by sequence analysis elsewhere) individually activate A alpha-regulated development when transformed into any strain with a different A alpha mating type. The only exceptions are when the Y alleles of A alpha 3 or A alpha 4 (i.e., Y3 or Y4, respectively) are introduced into an A alpha 1 strain (the A alpha 1 locus encodes Y1 but lacks a Z gene). These observations indicate that A alpha-regulated development is activated by the interaction (direct or indirect) of products from different genes (e.g., Z3 and Y1) rather than from different alleles of the same gene (e.g., Y1 and Y3). Therefore, the activating interaction is of the form ZiYj where i not equal to j and i and j are the A alpha mating types from which the Z and Y polypeptides, respectively, are derived. Transformations with truncated or mutagenized genes begin to define essential regions of the genes and their products. Activity is in some cases dependent upon the particular A alpha mating type of the recipient. A working hypothesis for the activation of A alpha-regulated development is proposed.

Crosses, Genetic

Transmission of mitochondrial DNA in Ustilago violacea.

Mitochondrial DNA (mtDNA) restriction fragment length polymorphisms (RFLPs) were used as genetic markers for following mitochondrial transmission in the basidiomycete Ustilago violacea. Yeast-like cells of opposite mating types (a1 and a2) were mated on 2% water agar and were treated with alpha-tocopherol to induce formation of dikaryotic hyphae. Upon depletion of the alpha-tocopherol, the hyphae budded off haploid cells with parental nuclear genotypes. These cells were examined for mitochondrial RFLP phenotype. In progeny expressing the a1 mating type, mitochondria from either parent were observed equally frequently. In progeny with the a2 mating type, mitochondria were almost exclusively (94%) from the a2 parent.

Crosses, Genetic