Evidence map›Paper›PMID 32807079›Full record

ArticleBMC genomics2020

Relatively semi-conservative replication and a folded slippage model for short tandem repeats.

Hongxi Zhang, Douyue Li, Xiangyan Zhao, Saichao Pan, Xiaolong Wu, Shan Peng, Hanrou Huang, Ruixue Shi, Zhongyang Tan

Abstract read
In one paragraph

Article in BMC genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. ULTRA-Effective Labeling of Repetitive Genomic Sequence.bioRxiv : the preprint server for biology · 2024
    Article
  5. Article
  6. Genome-wide development and application of miRNA-SSR markers inPhysiology and molecular biology of plants : an international journal of functional plant biology · 2021
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Hongxi ZhangBioinformatics Center, College of Biology, Hunan University, Changsha, 410082, China.
Douyue LiBioinformatics Center, College of Biology, Hunan University, Changsha, 410082, China.
Xiangyan ZhaoBioinformatics Center, College of Biology, Hunan University, Changsha, 410082, China.
Saichao PanBioinformatics Center, College of Biology, Hunan University, Changsha, 410082, China.
Xiaolong WuBioinformatics Center, College of Biology, Hunan University, Changsha, 410082, China.
Shan PengBioinformatics Center, College of Biology, Hunan University, Changsha, 410082, China.
Hanrou HuangBioinformatics Center, College of Biology, Hunan University, Changsha, 410082, China.
Ruixue ShiBioinformatics Center, College of Biology, Hunan University, Changsha, 410082, China.
Zhongyang TanBioinformatics Center, College of Biology, Hunan University, Changsha, 410082, China. zhongyangtan@yeah.net.

Funding

National Key Plan for Scientific Research and Development of China 2016YFC1200200National Key Plan for Scientific Research and Development of China 2016YFD0500300
6 · The paper itself

Abstract

backgroundThe ubiquitous presence of short tandem repeats (STRs) in virtually all genomes implicates their functional relevance, while a widely-accepted definition of STR is yet to be established. Previous studies majorly focus on relatively longer STRs, while shorter repeats were generally excluded. Herein, we have adopted a more generous criteria to define shorter repeats, which has led to the definition of a much larger number of STRs that lack prior analysis. Using this definition, we analyzed the short repeats in 55 randomly selected segments in 55 randomly selected genomic sequences from a fairly wide range of species covering animals, plants, fungi, protozoa, bacteria, archaea and viruses.

resultsOur analysis reveals a high percentage of short repeats in all 55 randomly selected segments, indicating that the universal presence of high-content short repeats could be a common characteristic of genomes across all biological kingdoms. Therefore, it is reasonable to assume a mechanism for continuous production of repeats that can make the replicating process relatively semi-conservative. We have proposed a folded replication slippage model that considers the geometric space of nucleotides and hydrogen bond stability to explain the mechanism more explicitly, with improving the existing straight-line slippage model. The folded slippage model can explain the expansion and contraction of mono- to hexa- nucleotide repeats with proper folding angles. Analysis of external forces in the folding template strands also suggests that expansion exists more commonly than contraction in the short tandem repeats.

conclusionThe folded replication slippage model provides a reasonable explanation for the continuous occurrences of simple sequence repeats in genomes. This model also contributes to the explanation of STR-to-genome evolution and is an alternative model that complements semi-conservative replication.

Indexed as

GenomeMicrosatellite RepeatsAnimalsGenomics

Identifiers

PMID32807079
PMCPMC7430839

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.