Literature DB >> 27322544

Parent-of-origin-specific signatures of de novo mutations.

Jakob M Goldmann1, Wendy S W Wong2, Michele Pinelli3, Terry Farrah4, Dale Bodian2, Anna B Stittrich4, Gustavo Glusman4, Lisenka E L M Vissers5, Alexander Hoischen5, Jared C Roach4, Joseph G Vockley2,6, Joris A Veltman5,7, Benjamin D Solomon2,8,9, Christian Gilissen5, John E Niederhuber2,9.   

Abstract

De novo mutations (DNMs) originating in gametogenesis are an important source of genetic variation. We use a data set of 7,216 autosomal DNMs with resolved parent of origin from whole-genome sequencing of 816 parent-offspring trios to investigate differences between maternally and paternally derived DNMs and study the underlying mutational mechanisms. Our results show that the number of DNMs in offspring increases not only with paternal age, but also with maternal age, and that some genome regions show enrichment for maternally derived DNMs. We identify parent-of-origin-specific mutation signatures that become more pronounced with increased parental age, pointing to different mutational mechanisms in spermatogenesis and oogenesis. Moreover, we find DNMs that are spatially clustered to have a unique mutational signature with no significant differences between parental alleles, suggesting a different mutational mechanism. Our findings provide insights into the molecular mechanisms that underlie mutagenesis and are relevant to disease and evolution in humans.

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Year:  2016        PMID: 27322544     DOI: 10.1038/ng.3597

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  39 in total

1.  Computational techniques for human genome resequencing using mated gapped reads.

Authors:  Paolo Carnevali; Jonathan Baccash; Aaron L Halpern; Igor Nazarenko; Geoffrey B Nilsen; Krishna P Pant; Jessica C Ebert; Anushka Brownley; Matt Morenzoni; Vitali Karpinchyk; Bruce Martin; Dennis G Ballinger; Radoje Drmanac
Journal:  J Comput Biol       Date:  2011-12-16       Impact factor: 1.479

2.  Genome sequencing identifies major causes of severe intellectual disability.

Authors:  Christian Gilissen; Jayne Y Hehir-Kwa; Djie Tjwan Thung; Maartje van de Vorst; Bregje W M van Bon; Marjolein H Willemsen; Michael Kwint; Irene M Janssen; Alexander Hoischen; Annette Schenck; Richard Leach; Robert Klein; Rick Tearle; Tan Bo; Rolph Pfundt; Helger G Yntema; Bert B A de Vries; Tjitske Kleefstra; Han G Brunner; Lisenka E L M Vissers; Joris A Veltman
Journal:  Nature       Date:  2014-06-04       Impact factor: 49.962

3.  Variation in genome-wide mutation rates within and between human families.

Authors:  Donald F Conrad; Jonathan E M Keebler; Mark A DePristo; Sarah J Lindsay; Yujun Zhang; Ferran Casals; Youssef Idaghdour; Chris L Hartl; Carlos Torroja; Kiran V Garimella; Martine Zilversmit; Reed Cartwright; Guy A Rouleau; Mark Daly; Eric A Stone; Matthew E Hurles; Philip Awadalla
Journal:  Nat Genet       Date:  2011-06-12       Impact factor: 38.330

Review 4.  Determinants of mutation rate variation in the human germline.

Authors:  Laure Ségurel; Minyoung J Wyman; Molly Przeworski
Journal:  Annu Rev Genomics Hum Genet       Date:  2014-06-05       Impact factor: 8.929

5.  A user's guide to the encyclopedia of DNA elements (ENCODE).

Authors: 
Journal:  PLoS Biol       Date:  2011-04-19       Impact factor: 8.029

6.  Genome-wide patterns and properties of de novo mutations in humans.

Authors:  Laurent C Francioli; Paz P Polak; Amnon Koren; Androniki Menelaou; Sung Chun; Ivo Renkens; Cornelia M van Duijn; Morris Swertz; Cisca Wijmenga; Gertjan van Ommen; P Eline Slagboom; Dorret I Boomsma; Kai Ye; Victor Guryev; Peter F Arndt; Wigard P Kloosterman; Paul I W de Bakker; Shamil R Sunyaev
Journal:  Nat Genet       Date:  2015-05-18       Impact factor: 38.330

7.  GEMINI: integrative exploration of genetic variation and genome annotations.

Authors:  Umadevi Paila; Brad A Chapman; Rory Kirchner; Aaron R Quinlan
Journal:  PLoS Comput Biol       Date:  2013-07-18       Impact factor: 4.475

8.  New observations on maternal age effect on germline de novo mutations.

Authors:  Wendy S W Wong; Benjamin D Solomon; Dale L Bodian; Prachi Kothiyal; Greg Eley; Kathi C Huddleston; Robin Baker; Dzung C Thach; Ramaswamy K Iyer; Joseph G Vockley; John E Niederhuber
Journal:  Nat Commun       Date:  2016-01-19       Impact factor: 14.919

9.  B cell super-enhancers and regulatory clusters recruit AID tumorigenic activity.

Authors:  Jason Qian; Qiao Wang; Marei Dose; Nathanael Pruett; Kyong-Rim Kieffer-Kwon; Wolfgang Resch; Genqing Liang; Zhonghui Tang; Ewy Mathé; Christopher Benner; Wendy Dubois; Steevenson Nelson; Laura Vian; Thiago Y Oliveira; Mila Jankovic; Ofir Hakim; Anna Gazumyan; Rushad Pavri; Parirokh Awasthi; Bin Song; Geng Liu; Longyun Chen; Shida Zhu; Lionel Feigenbaum; Louis Staudt; Cornelis Murre; Yijun Ruan; Davide F Robbiani; Qiang Pan-Hammarström; Michel C Nussenzweig; Rafael Casellas
Journal:  Cell       Date:  2014-12-04       Impact factor: 41.582

10.  Integrative analysis of 111 reference human epigenomes.

Authors:  Anshul Kundaje; Wouter Meuleman; Jason Ernst; Misha Bilenky; Angela Yen; Alireza Heravi-Moussavi; Pouya Kheradpour; Zhizhuo Zhang; Jianrong Wang; Michael J Ziller; Viren Amin; John W Whitaker; Matthew D Schultz; Lucas D Ward; Abhishek Sarkar; Gerald Quon; Richard S Sandstrom; Matthew L Eaton; Yi-Chieh Wu; Andreas R Pfenning; Xinchen Wang; Melina Claussnitzer; Yaping Liu; Cristian Coarfa; R Alan Harris; Noam Shoresh; Charles B Epstein; Elizabeta Gjoneska; Danny Leung; Wei Xie; R David Hawkins; Ryan Lister; Chibo Hong; Philippe Gascard; Andrew J Mungall; Richard Moore; Eric Chuah; Angela Tam; Theresa K Canfield; R Scott Hansen; Rajinder Kaul; Peter J Sabo; Mukul S Bansal; Annaick Carles; Jesse R Dixon; Kai-How Farh; Soheil Feizi; Rosa Karlic; Ah-Ram Kim; Ashwinikumar Kulkarni; Daofeng Li; Rebecca Lowdon; GiNell Elliott; Tim R Mercer; Shane J Neph; Vitor Onuchic; Paz Polak; Nisha Rajagopal; Pradipta Ray; Richard C Sallari; Kyle T Siebenthall; Nicholas A Sinnott-Armstrong; Michael Stevens; Robert E Thurman; Jie Wu; Bo Zhang; Xin Zhou; Arthur E Beaudet; Laurie A Boyer; Philip L De Jager; Peggy J Farnham; Susan J Fisher; David Haussler; Steven J M Jones; Wei Li; Marco A Marra; Michael T McManus; Shamil Sunyaev; James A Thomson; Thea D Tlsty; Li-Huei Tsai; Wei Wang; Robert A Waterland; Michael Q Zhang; Lisa H Chadwick; Bradley E Bernstein; Joseph F Costello; Joseph R Ecker; Martin Hirst; Alexander Meissner; Aleksandar Milosavljevic; Bing Ren; John A Stamatoyannopoulos; Ting Wang; Manolis Kellis
Journal:  Nature       Date:  2015-02-19       Impact factor: 69.504

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  101 in total

1.  Age-related accumulation of de novo mitochondrial mutations in mammalian oocytes and somatic tissues.

Authors:  Barbara Arbeithuber; James Hester; Marzia A Cremona; Nicholas Stoler; Arslan Zaidi; Bonnie Higgins; Kate Anthony; Francesca Chiaromonte; Francisco J Diaz; Kateryna D Makova
Journal:  PLoS Biol       Date:  2020-07-15       Impact factor: 8.029

2.  Distinct error rates for reference and nonreference genotypes estimated by pedigree analysis.

Authors:  Richard J Wang; Predrag Radivojac; Matthew W Hahn
Journal:  Genetics       Date:  2021-03-03       Impact factor: 4.562

3.  Decoding germline de novo point mutations.

Authors:  Anne Goriely
Journal:  Nat Genet       Date:  2016-07-27       Impact factor: 38.330

4.  Parental Age and Risk of Infant Leukaemia: A Pooled Analysis.

Authors:  Erin L Marcotte; Todd E Druley; Kimberly J Johnson; Michaela Richardson; Julie von Behren; Beth A Mueller; Susan Carozza; Colleen McLaughlin; Eric J Chow; Peggy Reynolds; Logan G Spector
Journal:  Paediatr Perinat Epidemiol       Date:  2017-09-22       Impact factor: 3.980

Review 5.  When the Lyon(ized chromosome) roars: ongoing expression from an inactive X chromosome.

Authors:  Laura Carrel; Carolyn J Brown
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2017-11-05       Impact factor: 6.237

6.  Germline de novo mutation clusters arise during oocyte aging in genomic regions with high double-strand-break incidence.

Authors:  Jakob M Goldmann; Vladimir B Seplyarskiy; Wendy S W Wong; Thierry Vilboux; Pieter B Neerincx; Dale L Bodian; Benjamin D Solomon; Joris A Veltman; John F Deeken; Christian Gilissen; John E Niederhuber
Journal:  Nat Genet       Date:  2018-03-05       Impact factor: 38.330

7.  The DNA double-strand "breakome" of mouse spermatids.

Authors:  Marie-Chantal Grégoire; Frédéric Leduc; Martin H Morin; Tiphanie Cavé; Mélina Arguin; Martin Richter; Pierre-Étienne Jacques; Guylain Boissonneault
Journal:  Cell Mol Life Sci       Date:  2018-02-07       Impact factor: 9.261

8.  Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks.

Authors:  Elizabeth K Ruzzo; Laura Pérez-Cano; Jae-Yoon Jung; Lee-Kai Wang; Dorna Kashef-Haghighi; Chris Hartl; Chanpreet Singh; Jin Xu; Jackson N Hoekstra; Olivia Leventhal; Virpi M Leppä; Michael J Gandal; Kelley Paskov; Nate Stockham; Damon Polioudakis; Jennifer K Lowe; David A Prober; Daniel H Geschwind; Dennis P Wall
Journal:  Cell       Date:  2019-08-08       Impact factor: 41.582

9.  Reproductive Longevity Predicts Mutation Rates in Primates.

Authors:  Gregg W C Thomas; Richard J Wang; Arthi Puri; R Alan Harris; Muthuswamy Raveendran; Daniel S T Hughes; Shwetha C Murali; Lawrence E Williams; Harsha Doddapaneni; Donna M Muzny; Richard A Gibbs; Christian R Abee; Mary R Galinski; Kim C Worley; Jeffrey Rogers; Predrag Radivojac; Matthew W Hahn
Journal:  Curr Biol       Date:  2018-09-27       Impact factor: 10.834

10.  Parental Age and Offspring Psychopathology in the Philadelphia Neurodevelopmental Cohort.

Authors:  Alison K Merikangas; Monica E Calkins; Warren B Bilker; Tyler M Moore; Ruben C Gur; Raquel E Gur
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  2017-03-06       Impact factor: 8.829

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