Evidence map›Paper›PMID 31108506›Full record

ArticleHuman molecular genetics2019

Evolutionary and functional analysis of RBMY1 gene copy number variation on the human Y chromosome.

Wentao Shi, Sandra Louzada, Marina Grigorova, Andrea Massaia, Elena Arciero, Laura Kibena, Xiangyu Jack Ge, Yuan Chen, Qasim Ayub, Olev Poolamets and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Human molecular genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

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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

16 authors at 6 institutions in 4 countries.

Wentao ShiWellcome Genome Campus, Wellcome Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Sandra LouzadaWellcome Genome Campus, Wellcome Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Marina GrigorovaInstitute of Biomedicine and Translational Medicine, University of Tartu, Tartu 50411, Estonia.
Andrea MassaiaWellcome Genome Campus, Wellcome Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Elena ArcieroWellcome Genome Campus, Wellcome Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Laura KibenaInstitute of Biomedicine and Translational Medicine, University of Tartu, Tartu 50411, Estonia.
Xiangyu Jack GeWellcome Genome Campus, Wellcome Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Yuan ChenWellcome Genome Campus, Wellcome Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Qasim AyubWellcome Genome Campus, Wellcome Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Olev PoolametsAndrology Unit, Tartu University Hospital, Tartu 50406, Estonia.
Chris Tyler-SmithWellcome Genome Campus, Wellcome Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Margus PunabAndrology Unit, Tartu University Hospital, Tartu 50406, Estonia.
Maris LaanInstitute of Biomedicine and Translational Medicine, University of Tartu, Tartu 50411, Estonia.
Fengtang YangWellcome Genome Campus, Wellcome Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Pille HallastWellcome Genome Campus, Wellcome Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Yali XueWellcome Genome Campus, Wellcome Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Wellcome Sanger Institute · GBUniversity of Tartu · EETartu University Hospital · EEMonash University Malaysia · MYTianjin Medical University · CNUniversity of Manchester · GB

Funding

Wellcome Trust 098051
6 · The paper itself

Abstract

Human RBMY1 genes are located in four variable-sized clusters on the Y chromosome, expressed in male germ cells and possibly associated with sperm motility. We have re-investigated the mutational background and evolutionary history of the RBMY1 copy number distribution in worldwide samples and its relevance to sperm parameters in an Estonian cohort of idiopathic male factor infertility subjects. We estimated approximate RBMY1 copy numbers in 1218 1000 Genomes Project phase 3 males from sequencing read-depth, then chose 14 for valid ation by multicolour fibre-FISH. These fibre-FISH samples provided accurate calibration standards for the entire panel and led to detailed insights into population variation and mutational mechanisms. RBMY1 copy number worldwide ranged from 3 to 13 with a mode of 8. The two larger proximal clusters were the most variable, and additional duplications, deletions and inversions were detected. Placing the copy number estimates onto the published Y-SNP-based phylogeny of the same samples suggested a minimum of 562 mutational changes, translating to a mutation rate of 2.20 × 10-3 (95% CI 1.94 × 10-3 to 2.48 × 10-3) per father-to-son Y-transmission, higher than many short tandem repeat (Y-STRs), and showed no evidence for selection for increased or decreased copy number, but possible copy number stabilizing selection. An analysis of RBMY1 copy numbers among 376 infertility subjects failed to replicate a previously reported association with sperm motility and showed no significant effect on sperm count and concentration, serum follicle stimulating hormone (FSH), luteinizing hormone (LH) and testosterone levels or testicular and semen volume. These results provide the first in-depth insights into the structural rearrangements underlying RBMY1 copy number variation across diverse human lineages.

Indexed as

Chromosomes, Human, YDNA Copy Number VariationsEvolution, MolecularComparative Genomic HybridizationGenome, HumanGenomicsHumansIn Situ Hybridization, FluorescenceMaleMultigene FamilyMutationNuclear ProteinsPhylogenyRNA-Binding ProteinsSpermatozoaNuclear ProteinsRBMY1A1 protein, humanRNA-Binding Proteins

Identifiers

PMID31108506
PMCPMC6687947
OpenAlexW2945682732

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.