Literature DB >> 21034672

TRPing up the genome: Tandem repeat polymorphisms as dynamic sources of genetic variability in health and disease.

Anthony J Hannan1.   

Abstract

Repetitive DNA sequences constitute a large fraction of the genomes of humans and other animal species. Tandem repeats are a major class of repetitive DNA and the extent of their polymorphic distributions and functions within the human genome are only beginning to be explored. Tandem repeat polymorphisms (TRPs) provide a unique source of genomic variability and recent evidence suggests they can modulate a range of biological processes, in developing and mature organisms. Tandem repeats can change length during meiosis and mitosis, providing a dynamic source of genetic variation which may not only influence evolutionary processes, but also somatic cellular selection. Furthermore, recent evidence for post-mitotic instability of specific tandem repeats in neurons supports their additional possible roles in neuronal function and dysfunction. The mutation rate of TRPs is higher and the extent of polymorphism is far more diverse than that of single nucleotide polymorphisms (SNPs). Whereas SNPs are invariably binary in nature, TRPs generally exhibit extended digital (multiallelic) distributions, which provide a much richer range of polymorphic variants, and thus a wider possible range of genetic contribution to disease susceptibility. Expansions in tandem repeats are known to cause many monogenic disorders, which mainly affect the nervous system, including Huntington's disease, various spinocerebellar ataxias, other polyglutamine diseases, Friedreich ataxia, fragile X syndrome, myoclonic epilepsy, polyalanine disorders, and myotonic dystrophy. Furthermore, it has recently been proposed that TRPs could help solve the conundrum of "missing heritability" produced by SNP-based genome-wide association studies of various polygenic complex diseases. There are hundreds of thousands of unique tandem repeats in the human genome and their polymorphic distributions have the potential to greatly influence functional diversity and disease susceptibility. Recent discoveries in this expanding field are discussed, with a focus on the role of TRPs in brain development, function, and dysfunction.

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Year:  2010        PMID: 21034672

Source DB:  PubMed          Journal:  Discov Med        ISSN: 1539-6509            Impact factor:   2.970


  15 in total

1.  Sex-specific effects of the Huntington gene on normal neurodevelopment.

Authors:  Jessica K Lee; Yue Ding; Amy L Conrad; Elena Cattaneo; Eric Epping; Kathy Mathews; Pedro Gonzalez-Alegre; Larry Cahill; Vincent Magnotta; Bradley L Schlaggar; Joel S Perlmutter; Regina E Y Kim; Jeffrey D Dawson; Peg Nopoulos
Journal:  J Neurosci Res       Date:  2017-01-02       Impact factor: 4.164

Review 2.  Multiple cellular mechanisms prevent chromosomal rearrangements involving repetitive DNA.

Authors:  Carolyn M George; Eric Alani
Journal:  Crit Rev Biochem Mol Biol       Date:  2012-04-12       Impact factor: 8.250

3.  LINE-1-derived poly(A) microsatellites undergo rapid shortening and create somatic and germline mosaicism in mice.

Authors:  Fiorella C Grandi; James M Rosser; Wenfeng An
Journal:  Mol Biol Evol       Date:  2012-11-02       Impact factor: 16.240

Review 4.  Explaining additional genetic variation in complex traits.

Authors:  Matthew R Robinson; Naomi R Wray; Peter M Visscher
Journal:  Trends Genet       Date:  2014-03-11       Impact factor: 11.639

5.  Sequencing and analysis of a South Asian-Indian personal genome.

Authors:  Ravi Gupta; Aakrosh Ratan; Changanamkandath Rajesh; Rong Chen; Hie Lim Kim; Richard Burhans; Webb Miller; Sam Santhosh; Ramana V Davuluri; Atul J Butte; Stephan C Schuster; Somasekar Seshagiri; George Thomas
Journal:  BMC Genomics       Date:  2012-08-31       Impact factor: 3.969

6.  Correlation of CAG repeat length between the maternal and paternal allele of the Huntingtin gene: evidence for assortative mating.

Authors:  Peg Nopoulos; Eric A Epping; Tom Wassink; Bradley L Schlaggar; Joel Perlmutter
Journal:  Behav Brain Funct       Date:  2011-10-18       Impact factor: 3.759

7.  Association of the FAM46A gene VNTRs and BAG6 rs3117582 SNP with non small cell lung cancer (NSCLC) in Croatian and Norwegian populations.

Authors:  Godfrey Essien Etokebe; Shanbeh Zienolddiny; Zeljko Kupanovac; Morten Enersen; Sanja Balen; Veljko Flego; Ljiljana Bulat-Kardum; Anđelka Radojčić-Badovinac; Vidar Skaug; Per Bakke; Aage Haugen; Zlatko Dembic
Journal:  PLoS One       Date:  2015-04-17       Impact factor: 3.240

Review 8.  Coherent somatic mutation in autoimmune disease.

Authors:  Kenneth Andrew Ross
Journal:  PLoS One       Date:  2014-07-02       Impact factor: 3.240

9.  Sequencing the unsequenceable: expanded CGG-repeat alleles of the fragile X gene.

Authors:  Erick W Loomis; John S Eid; Paul Peluso; Jun Yin; Luke Hickey; David Rank; Sarah McCalmon; Randi J Hagerman; Flora Tassone; Paul J Hagerman
Journal:  Genome Res       Date:  2012-10-11       Impact factor: 9.043

10.  Association of variable number of tandem repeats in the coding region of the FAM46A gene, FAM46A rs11040 SNP and BAG6 rs3117582 SNP with susceptibility to tuberculosis.

Authors:  Godfrey Essien Etokebe; Ljiljana Bulat-Kardum; Ludvig Andre Munthe; Sanja Balen; Zlatko Dembic
Journal:  PLoS One       Date:  2014-03-13       Impact factor: 3.240

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