Evidence map›Paper›PMID 28292260›Full record

ArticleBMC evolutionary biology2017

Ruminant-specific multiple duplication events of PRDM9 before speciation.

Abinash Padhi, Botong Shen, Jicai Jiang, Yang Zhou, George E Liu, Li Ma

Open access · goldAbstract read
In one paragraph

Article in BMC evolutionary biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 41% of its field
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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Construction of PRDM9 allele-specific recombination maps in cattle using large-scale pedigree analysis and genome-wide single sperm genomics.DNA research : an international journal for rapid publication of reports on genes and genomes · 2018
    Article
  2. PRDM9 and Its Role in Genetic Recombination.Trends in genetics : TIG · 2018
    Review
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

6 authors at 2 institutions in 2 countries.

Abinash PadhiDepartment of Animal and Avian Sciences, University of Maryland, College Park, MD, 20742, USA. bshen218@umd.edu.
Botong ShenDepartment of Animal and Avian Sciences, University of Maryland, College Park, MD, 20742, USA.
Jicai JiangDepartment of Animal and Avian Sciences, University of Maryland, College Park, MD, 20742, USA.
Yang ZhouAnimal Genomics and Improvement Laboratory, Agricultural Research Service, USDA, Beltsville, MD, 20705, USA.
George E LiuAnimal Genomics and Improvement Laboratory, Agricultural Research Service, USDA, Beltsville, MD, 20705, USA.
Li MaDepartment of Animal and Avian Sciences, University of Maryland, College Park, MD, 20742, USA. lima@umd.edu.
University of Maryland, College Park · USBeltsville Agricultural Research Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUnderstanding the genetic and evolutionary mechanisms of speciation genes in sexually reproducing organisms would provide important insights into mammalian reproduction and fitness. PRDM9, a widely known speciation gene, has recently gained attention for its important role in meiotic recombination and hybrid incompatibility. Despite the fact that PRDM9 is a key regulator of recombination and plays a dominant role in hybrid incompatibility, little is known about the underlying genetic and evolutionary mechanisms that generated multiple copies of PRDM9 in many metazoan lineages.

resultsThe present study reports (1) evidence of ruminant-specific multiple gene duplication events, which likely have had occurred after the ancestral ruminant population diverged from its most recent common ancestor and before the ruminant speciation events, (2) presence of three copies of PRDM9, one copy (lineages I) in chromosome 1 (chr1) and two copies (lineages II & III) in chromosome X (chrX), thus indicating the possibility of ancient inter- and intra-chromosomal unequal crossing over and gene conversion events, (3) while lineages I and II are characterized by the presence of variable tandemly repeated C2H2 zinc finger (ZF) arrays, lineage III lost these arrays, and (4) C2H2 ZFs of lineages I and II, particularly the amino acid residues located at positions -1, 3, and 6 have evolved under strong positive selection.

conclusionsOur results demonstrated two gene duplication events of PRDM9 in ruminants: an inter-chromosomal duplication that occurred between chr1 and chrX, and an intra-chromosomal X-linked duplication, which resulted in two additional copies of PRDM9 in ruminants. The observation of such duplication between chrX and chr1 is rare and may possibly have happened due to unequal crossing-over millions of years ago when sex chromosomes were independently derived from a pair of ancestral autosomes. Two copies (lineages I & II) are characterized by the presence of variable sized tandem-repeated C2H2 ZFs and evolved under strong positive selection and concerted evolution, supporting the notion of well-established Red Queen hypothesis. Collectively, gene duplication, concerted evolution, and positive selection are the likely driving forces for the expansion of ruminant PRDM9 sub-family.

Indexed as

Evolution, MolecularGenetic SpeciationAmino Acid SequenceAnimalsBiological EvolutionGene ConversionGene DuplicationHistone-Lysine N-MethyltransferaseMeiosisPhylogenyRecombination, GeneticRuminantsHistone-Lysine N-MethyltransferaseGene duplicationGenetic incompatibilityMolecular evolutionPositive selectionPRDM9RuminantsSpeciation genetics

Identifiers

PMID28292260
PMCPMC5351255
OpenAlexW2595133580

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.