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Simple sequences are ubiquitous repetitive components of eukaryotic genomes

Diethard Tautz, +1 more
- 25 May 1984 - 
- Vol. 12, Iss: 10, pp 4127-4138
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TLDR
Many, probably even all possible types of simple sequence are repetitive components of eukaryotic genomes and it is proposed that they arise by common mechanisms namely slippage replication and unequal crossover and that they might have no general function with regards to gene expression.
Abstract
Simple sequences are stretches of DNA which consist of only one, or a few tandemly repeated nucleotides, for example poly (dA) X poly (dT) or poly (dG-dT) X poly (dC-dA). These two types of simple sequence have been shown to be repetitive and interspersed in many eukaryotic genomes. Several other types have been found by sequencing eukaryotic DNA. In this report we have undertaken a systematical survey for simple sequences. We hybridized synthetical simple sequence DNA to genome blots of phylogenetically different organisms. We found that many, probably even all possible types of simple sequence are repetitive components of eukaryotic genomes. We propose therefore that they arise by common mechanisms namely slippage replication and unequal crossover and that they might have no general function with regards to gene expression. This latter inference is supported by the fact that we have detected simple sequences only in the metabolically inactive micronucleus of the protozoan Stylonychia, but not in the metabolically active macronucleus which is derived from the micronucleus by chromosome diminution.

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Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction

TL;DR: It is reported that specific human (dC-dA)n.(dG-dT)n blocks are polymorphic in length among individuals and therefore represent a vast new pool of potential genetic markers.
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The comparison of RFLP, RAPD, AFLP and SSR (microsatellite) markers for germplasm analysis

TL;DR: A comparison of genetic similarity matrices revealed that, if the comparison involved both cultivated and wild soybean accessions, estimates based on RFLPs, RAPD, AFLPs and SSRs are highly correlated, indicating congruence between these assays.
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Hypervariability of simple sequences as a general source for polymorphic DNA markers

TL;DR: The polymerase chain reaction (PCR) process is used to show that several randomly chosen simple sequence loci with different nucleotide composition and from different species show extensive length polymorphisms.
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Polymorphism revealed by simple sequence repeats

TL;DR: Simple sequence repeats are a group of repetitive DNA sequences that represent a significant portion of higher eukaryote genomes and can serve as highly informative genetic markers, and in conjunction with the use of polymerase chain reaction technology enable the detection of length variation.
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Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms.

TL;DR: The longest run of uninterrupted CA or GT repeats was found to be the best predictor of informativeness of (dC-dA)n.(dG-dT)n polymorphisms regardless of the repeat sequence category.
References
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Journal ArticleDOI

Detection of specific sequences among DNA fragments separated by gel electrophoresis.

TL;DR: This paper describes a method of transferring fragments of DNA from agarose gels to cellulose nitrate filters that can be hybridized to radioactive RNA and hybrids detected by radioautography or fluorography.
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The fractionation of high-molecular-weight ribonucleic acid by polyacrylamide-gel electrophoresis.

UE Loening
- 01 Jan 1967 - 
TL;DR: Electrophoresis in 2.2-2.6% gels gives a fractionation similar to density-gradient centrifugation, and the resolution is greater and more detailed than by centrifugations, and many samples can be analysed simultaneously and rapidly.
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Molecular drive: a cohesive mode of species evolution

TL;DR: There are circumstances in which the unusual concerted pattern of fixation permits the establishment of biological novelty and species discontinuities in a manner not predicted by the classical genetics of natural selection and genetic drift.
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Determination of nucleic acid sequence homologies and relative concentrations by a dot hybridization procedure

TL;DR: A dot hybridization method is presented for rapidly determining the relative concentrations of nucleic acids in a mixture, as well as the extent of sequence homology between related RNA or DNA species.
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