Literature DB >> 29476164

A genome-wide characterization of copy number variations in native populations of Peninsular Malaysia.

Ruiqing Fu1,2, Siti Shuhada Mokhtar3, Maude Elvira Phipps4, Boon-Peng Hoh1,5, Shuhua Xu6,7,8,9.   

Abstract

Copy number variations (CNVs) are genomic structural variations that result from the deletion or duplication of large genomic segments. The characterization of CNVs is largely underrepresented, particularly those of indigenous populations, such as the Orang Asli in Peninsular Malaysia. In the present study, we first characterized the genome-wide CNVs of four major native populations from Peninsular Malaysia, including the Malays and three Orang Asli populations; namely, Proto-Malay, Senoi, and Negrito (collectively called PM). We subsequently assessed the distribution of CNVs across the four populations. The resulting global CNV map revealed 3102 CNVs, with an average of more than 100 CNVs per individual. We identified genes harboring CNVs that are highly differentiated between PM and global populations, indicating that these genes are predominantly enriched in immune responses and defense functions, including APOBEC3A_B, beta-defensin genes, and CCL3L1, followed by other biological functions, such as drug and toxin metabolism and responses to radiation, suggesting some attributions between CNV variations and adaptations of the PM groups to the local environmental conditions of tropical rainforests.

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Year:  2018        PMID: 29476164      PMCID: PMC5974366          DOI: 10.1038/s41431-018-0120-8

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  43 in total

1.  Inference of population structure using multilocus genotype data.

Authors:  J K Pritchard; M Stephens; P Donnelly
Journal:  Genetics       Date:  2000-06       Impact factor: 4.562

2.  Inference of population structure using multilocus genotype data: linked loci and correlated allele frequencies.

Authors:  Daniel Falush; Matthew Stephens; Jonathan K Pritchard
Journal:  Genetics       Date:  2003-08       Impact factor: 4.562

3.  Principal components analysis corrects for stratification in genome-wide association studies.

Authors:  Alkes L Price; Nick J Patterson; Robert M Plenge; Michael E Weinblatt; Nancy A Shadick; David Reich
Journal:  Nat Genet       Date:  2006-07-23       Impact factor: 38.330

4.  Diet and the evolution of human amylase gene copy number variation.

Authors:  George H Perry; Nathaniel J Dominy; Katrina G Claw; Arthur S Lee; Heike Fiegler; Richard Redon; John Werner; Fernando A Villanea; Joanna L Mountain; Rajeev Misra; Nigel P Carter; Charles Lee; Anne C Stone
Journal:  Nat Genet       Date:  2007-09-09       Impact factor: 38.330

5.  Strong association of de novo copy number mutations with autism.

Authors:  Jonathan Sebat; B Lakshmi; Dheeraj Malhotra; Jennifer Troge; Christa Lese-Martin; Tom Walsh; Boris Yamrom; Seungtai Yoon; Alex Krasnitz; Jude Kendall; Anthony Leotta; Deepa Pai; Ray Zhang; Yoon-Ha Lee; James Hicks; Sarah J Spence; Annette T Lee; Kaija Puura; Terho Lehtimäki; David Ledbetter; Peter K Gregersen; Joel Bregman; James S Sutcliffe; Vaidehi Jobanputra; Wendy Chung; Dorothy Warburton; Mary-Claire King; David Skuse; Daniel H Geschwind; T Conrad Gilliam; Kenny Ye; Michael Wigler
Journal:  Science       Date:  2007-03-15       Impact factor: 47.728

Review 6.  Human gene copy number variation and infectious disease.

Authors:  Edward J Hollox; Boon-Peng Hoh
Journal:  Hum Genet       Date:  2014-06-05       Impact factor: 4.132

7.  Population genetic structure of peninsular Malaysia Malay sub-ethnic groups.

Authors:  Wan Isa Hatin; Ab Rajab Nur-Shafawati; Mohd-Khairi Zahri; Shuhua Xu; Li Jin; Soon-Guan Tan; Mohammed Rizman-Idid; Bin Alwi Zilfalil
Journal:  PLoS One       Date:  2011-04-05       Impact factor: 3.240

8.  Large recurrent microdeletions associated with schizophrenia.

Authors:  Hreinn Stefansson; Dan Rujescu; Sven Cichon; Olli P H Pietiläinen; Andres Ingason; Stacy Steinberg; Ragnheidur Fossdal; Engilbert Sigurdsson; Thordur Sigmundsson; Jacobine E Buizer-Voskamp; Thomas Hansen; Klaus D Jakobsen; Pierandrea Muglia; Clyde Francks; Paul M Matthews; Arnaldur Gylfason; Bjarni V Halldorsson; Daniel Gudbjartsson; Thorgeir E Thorgeirsson; Asgeir Sigurdsson; Adalbjorg Jonasdottir; Aslaug Jonasdottir; Asgeir Bjornsson; Sigurborg Mattiasdottir; Thorarinn Blondal; Magnus Haraldsson; Brynja B Magnusdottir; Ina Giegling; Hans-Jürgen Möller; Annette Hartmann; Kevin V Shianna; Dongliang Ge; Anna C Need; Caroline Crombie; Gillian Fraser; Nicholas Walker; Jouko Lonnqvist; Jaana Suvisaari; Annamarie Tuulio-Henriksson; Tiina Paunio; Timi Toulopoulou; Elvira Bramon; Marta Di Forti; Robin Murray; Mirella Ruggeri; Evangelos Vassos; Sarah Tosato; Muriel Walshe; Tao Li; Catalina Vasilescu; Thomas W Mühleisen; August G Wang; Henrik Ullum; Srdjan Djurovic; Ingrid Melle; Jes Olesen; Lambertus A Kiemeney; Barbara Franke; Chiara Sabatti; Nelson B Freimer; Jeffrey R Gulcher; Unnur Thorsteinsdottir; Augustine Kong; Ole A Andreassen; Roel A Ophoff; Alexander Georgi; Marcella Rietschel; Thomas Werge; Hannes Petursson; David B Goldstein; Markus M Nöthen; Leena Peltonen; David A Collier; David St Clair; Kari Stefansson
Journal:  Nature       Date:  2008-09-11       Impact factor: 49.962

9.  FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity.

Authors:  Manuela Fanciulli; Penny J Norsworthy; Enrico Petretto; Rong Dong; Lorraine Harper; Lavanya Kamesh; Joanne M Heward; Stephen C L Gough; Adam de Smith; Alexandra I F Blakemore; Philippe Froguel; Catherine J Owen; Simon H S Pearce; Luis Teixeira; Loic Guillevin; Deborah S Cunninghame Graham; Charles D Pusey; H Terence Cook; Timothy J Vyse; Timothy J Aitman
Journal:  Nat Genet       Date:  2007-05-21       Impact factor: 38.330

10.  Mechanisms for human genomic rearrangements.

Authors:  Wenli Gu; Feng Zhang; James R Lupski
Journal:  Pathogenetics       Date:  2008-11-03
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  6 in total

Review 1.  The Peopling and Migration History of the Natives in Peninsular Malaysia and Borneo: A Glimpse on the Studies Over the Past 100 years.

Authors:  Boon-Peng Hoh; Lian Deng; Shuhua Xu
Journal:  Front Genet       Date:  2022-01-27       Impact factor: 4.599

2.  Analysis of five deep-sequenced trio-genomes of the Peninsular Malaysia Orang Asli and North Borneo populations.

Authors:  Lian Deng; Haiyi Lou; Xiaoxi Zhang; Bhooma Thiruvahindrapuram; Dongsheng Lu; Christian R Marshall; Chang Liu; Bo Xie; Wanxing Xu; Lai-Ping Wong; Chee-Wei Yew; Aghakhanian Farhang; Rick Twee-Hee Ong; Mohammad Zahirul Hoque; Abdul Rahman Thuhairah; Bhak Jong; Maude E Phipps; Stephen W Scherer; Yik-Ying Teo; Subbiah Vijay Kumar; Boon-Peng Hoh; Shuhua Xu
Journal:  BMC Genomics       Date:  2019-11-12       Impact factor: 3.969

3.  Genome-wide copy number variations in a large cohort of bantu African children.

Authors:  Feyza Yilmaz; Megan Null; David Astling; Hung-Chun Yu; Joanne Cole; Stephanie A Santorico; Benedikt Hallgrimsson; Mange Manyama; Richard A Spritz; Audrey E Hendricks; Tamim H Shaikh
Journal:  BMC Med Genomics       Date:  2021-05-17       Impact factor: 3.063

4.  A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa.

Authors:  Lilia Romdhane; Nessrine Mezzi; Hamza Dallali; Olfa Messaoud; Jingxuan Shan; Khalid A Fakhro; Rym Kefi; Lotfi Chouchane; Sonia Abdelhak
Journal:  NPJ Genom Med       Date:  2021-01-08       Impact factor: 8.617

5.  Copy number variation of CCL3L1 among three major ethnic groups in Malaysia.

Authors:  Jalilah Jamaluddin; Nur Khairina Mohd Khair; Shameni Devi Vinodamaney; Zulkefley Othman; Suhaili Abubakar
Journal:  BMC Genet       Date:  2020-01-03       Impact factor: 2.797

6.  The Functions of β-Defensin in Flounder (Paralichthys olivaceus): Antibiosis, Chemotaxis and Modulation of Phagocytosis.

Authors:  Xiaokai Hao; Heng Chi; Xiaoqian Tang; Jing Xing; Xiuzhen Sheng; Wenbin Zhan
Journal:  Biology (Basel)       Date:  2021-11-29
  6 in total

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