Old origin of a protective endogenous retrovirus (enJSRV) in the Ovis genus.

Heredity (Edinb)

Université Grenoble Alpes, Université Savoie Mont Blanc, CNRS, LECA, Grenoble, F-38000, France.

Published: February 2019

Sheep, the Jaagsiekte sheep retrovirus (JSRV) and its endogenous forms (enJSRVs) are a good model to study long-time relationships between retroviruses and their hosts. Taking advantage of 76 whole genome resequencing data of wild and domestic Ovis, we investigated the evolution of this relationship. An innovative analysis of re-sequencing data allowed characterizing 462 enJSRVs insertion sites (including 435 newly described insertions) in the Ovis genus. We focused our study on endogenous copies inserted in the q13 locus of chromosome 6 (6q13). Those copies are known to confer resistance against exogenous JSRV thanks to alleles bearing a mutation in the gag gene. We characterized (i) the distribution of protective and non-protective alleles across Ovis species and (ii) the copy number variation of the 6q13 locus. Our results challenged the previous hypothesis of fixation and amplification of the protective copies in relation with domestication, and allowed building a new model for the evolution of the 6q13 locus. JSRV would have integrated the 6q13 locus after the Ovis-Capra divergence (5-11 MYA) and before the Ovis diversification (2.4-5 MYA). The protective mutation in the enJSRV 6q13 copy appeared shortly after its insertion and was followed by genomic amplifications, after the divergence between Pachyform lineage on one side and the Argaliform and moufloniform lineages on the other (2.4-5 MYA). Considering the potential selective advantage of the protective mutation, its fixation in both sheep and its closest wild relative Ovis orientalis may be due to natural selection before domestication from O. orientalis populations.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327021PMC
http://dx.doi.org/10.1038/s41437-018-0112-zDOI Listing

Publication Analysis

Top Keywords

6q13 locus
12
ovis genus
8
24-5 mya
8
protective mutation
8
ovis
6
6q13
5
origin protective
4
protective endogenous
4
endogenous retrovirus
4
retrovirus enjsrv
4

Similar Publications

Association of SUMOylation Pathway Genes With Stroke in a Genome-Wide Association Study in India.

Neurology

July 2021

From the Department of Neurology (A.K., A.K.S., D.V., R.S., R.R., A.M., K.P.), Department of Neurobiochemisty (S.V.), Dr. R. P. Centre for Ophthalmic Sciences (D.M.), and Cardio-Neuro Centre (A.H.), All India Institute of Medical Sciences, New Delhi; Centre for Brain Research (G.C.), Indian Institute of Science, Bangalore; Department of Neurology (S.S.), North Eastern Indira Gandhi Regional Institute of Health and Medical Sciences, Shillong, Meghalaya; Department of Neurology (S.D.), Pandit Bhagwat Dayal Sharma Post Graduate Institute of Medical Sciences, Rohtak, Haryana; Department of Neurology (P.N.S.), Sree Chitra Tirunal Institute for Medical Sciences and Technology, Kerala; Department of Neurology (N.C., B.K., S.R.), Vardhman Mahavir Medical College and Safdarjung Hospital; Department of Neurology (S.G., S.P.G.), Army Research and Referral Hospital; Department of Neurology (C.S.A.), Sir Ganga Ram Hospital; Ram Manohar Lohia Hospital (K.S.A.); Department of Biotechnology (S.K.), Maharshi Dayanand University, Government of India, New Delhi; Pandit Bhagwat Dayal Sharma Post Graduate Institute of Medical Sciences (R.K.Y.), Rohtak, Haryana, India; and Institute of Cardiovascular Research Royal Holloway (P.S.), University of London, Imperial College London, UK. Amit Kumar, Kameshwar Prasad, and Ganesh Chauhan are currently at Rajendra Institute of Medical Sciences, Ranchi, India.

Objective: To undertake a genome-wide association study (GWAS) to identify genetic variants for stroke in an Indian population.

Methods: In a hospital-based case-control study, 8 teaching hospitals in India recruited 4,088 participants, including 1,609 stroke cases. Imputed genetic variants were tested for association with stroke subtypes using both single-marker and gene-based tests.

View Article and Find Full Text PDF

Old origin of a protective endogenous retrovirus (enJSRV) in the Ovis genus.

Heredity (Edinb)

February 2019

Université Grenoble Alpes, Université Savoie Mont Blanc, CNRS, LECA, Grenoble, F-38000, France.

Sheep, the Jaagsiekte sheep retrovirus (JSRV) and its endogenous forms (enJSRVs) are a good model to study long-time relationships between retroviruses and their hosts. Taking advantage of 76 whole genome resequencing data of wild and domestic Ovis, we investigated the evolution of this relationship. An innovative analysis of re-sequencing data allowed characterizing 462 enJSRVs insertion sites (including 435 newly described insertions) in the Ovis genus.

View Article and Find Full Text PDF

The recurrent 9p24.1 aberrations in lymphoid malignancies potentially involving four cancer-related and druggable genes (JAK2, CD274/PDL1, PDCD1LG2/PDL2, and KDM4C/JMJD2Cl) are incompletely characterized. To gain more insight into the anatomy of these abnormalities, at first we studied 9p24.

View Article and Find Full Text PDF
Article Synopsis
  • - The DEK-NUP214 gene fusion in acute myeloid leukemia (AML) is linked to a poor prognosis, typically occurring as a sole translocation, but complex chromosomal forms can also appear.
  • - In a specific AML case, complex karyotype abnormalities were found along with RNA sequencing revealing fusions between NUP214, RAC1, and COL12A1 genes.
  • - Analysis indicated that although the NUP214 and RAC1 fusions do not match in reading frame, high levels of RAC1 protein were produced, suggesting an important role of these complex gene fusions in AML.
View Article and Find Full Text PDF

A genome-wide association study of periodontitis in a Japanese population.

J Dent Res

April 2015

Department of Oral Rehabilitation, Division of Periodontology and Endodontology, School of Dentistry, Health Sciences University of Hokkaido, Tobetsu-cho, Ishikari, Hokkaido, Japan

Periodontitis is a multifactorial disease in which bacterial, lifestyle, and genetic factors are involved. Although previous genetic association studies identified several susceptibility genes for periodontitis in European populations, there is little information for Asian populations. Here, we conducted a genome-wide association study and a replication study consisting of 2,760 Japanese periodontitis patients and 15,158 Japanese controls.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!