Literature DB >> 10205898

Intimate association of microsatellite repeats with retrotransposons and other dispersed repetitive elements in barley.

L Ramsay1, M Macaulay, L Cardle, M Morgante, S degli Ivanissevich, E Maestri, W Powell, R Waugh.   

Abstract

Simple sequence repeat (SSR)-based genetic markers are being actively developed for the majority of crop plant species. In barley, characterization of 290 dinucleotide repeat-containing clones from SSR-enriched libraries has revealed that a high percentage are associated with cereal retrotransposon-like and other dispersed repetitive elements. Associations found were with BARE-1, WIS2-1A, PREM1 and the dispersed repetitive element R173. Additional similarities between different SSR clones, which have no matches in DNA sequence databases, indicate that this phenomenon is probably widespread in the barley genome. Sequence homologies to the non-coding regions of several cereal genes were also explained by homology to mobile genetic elements. The SSRs found can therefore be classified into two types: (1) those with unique sequences on either flank, and (2) those which are intimately associated with retro-transposons and other dispersed repetitive elements. As the cereal genome is thought to consist largely of this type of DNA, some random association would be expected. However, the conserved positions of the SSRs, relative to repetitive elements, indicate that they have arisen non-randomly. Furthermore, this class of SSRs can be classified into three subtypes: (1) those which are positioned 3' of a transposable element with unique sequence on the other flank, (2) those positioned 5' of a transposable element, and (3) those which have arisen from an internal sequence and so have transposable element sequence on both flanks. The first appear to be analogous to the class of SSRs in mammalian systems which are associated with Alu elements and SINEs (short interspersed elements) and which have been postulated to arise following integration of an extended and polyadenylated retro-transcript into the host genome, followed by mutation of the poly(A) tract and expansion into an SSR. For the second, we postulate that a proto-SSR (A-rich sequence) has acted as a 'landing pad' for transposable element insertion (rather than being the result of insertion), while the third includes those which have evolved as a component of an active transposable element which has spread throughout the genome during bursts of transposition activity. The implications of these associations for genome and SSR evolution in barley are discussed.

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Year:  1999        PMID: 10205898     DOI: 10.1046/j.1365-313x.1999.00392.x

Source DB:  PubMed          Journal:  Plant J        ISSN: 0960-7412            Impact factor:   6.417


  56 in total

1.  Retrotransposon BARE-1 and Its Role in Genome Evolution in the Genus Hordeum.

Authors: 
Journal:  Plant Cell       Date:  1999-09       Impact factor: 11.277

2.  A simple sequence repeat-based linkage map of barley.

Authors:  L Ramsay; M Macaulay; S degli Ivanissevich; K MacLean; L Cardle; J Fuller; K J Edwards; S Tuvesson; M Morgante; A Massari; E Maestri; N Marmiroli; T Sjakste; M Ganal; W Powell; R Waugh
Journal:  Genetics       Date:  2000-12       Impact factor: 4.562

3.  Computational and experimental characterization of physically clustered simple sequence repeats in plants.

Authors:  L Cardle; L Ramsay; D Milbourne; M Macaulay; D Marshall; R Waugh
Journal:  Genetics       Date:  2000-10       Impact factor: 4.562

4.  Conserved simple sequence repeats for the Limnanthaceae (Brassicales).

Authors:  V K Kishore; P Velasco; D K Shintani; J Rowe; C Rosato; N Adair; M B Slabaugh; S J Knapp
Journal:  Theor Appl Genet       Date:  2003-11-27       Impact factor: 5.699

5.  Development of a genome-wide anchored microsatellite map for common bean (Phaseolus vulgaris L.).

Authors:  M W Blair; F Pedraza; H F Buendia; E Gaitán-Solís; S E Beebe; P Gepts; J Tohme
Journal:  Theor Appl Genet       Date:  2003-09-20       Impact factor: 5.699

6.  Comparative genomic analysis reveals species-dependent complexities that explain difficulties with microsatellite marker development in molluscs.

Authors:  C E McInerney; A L Allcock; M P Johnson; D A Bailie; P A Prodöhl
Journal:  Heredity (Edinb)       Date:  2010-04-28       Impact factor: 3.821

7.  Development of simple sequence repeat (SSR) markers and construction of an SSR-based linkage map in Italian ryegrass (Lolium multiflorum Lam.).

Authors:  Mariko Hirata; Hongwei Cai; Maiko Inoue; Nana Yuyama; Yuichi Miura; Toshinori Komatsu; Tadashi Takamizo; Masahiro Fujimori
Journal:  Theor Appl Genet       Date:  2006-05-11       Impact factor: 5.699

Review 8.  Mutational dynamics of microsatellites.

Authors:  Atul Bhargava; F F Fuentes
Journal:  Mol Biotechnol       Date:  2010-03       Impact factor: 2.695

9.  Talua SINE biology in the genome of the Reticulitermes subterranean termites (Isoptera, Rhinotermitidae).

Authors:  Andrea Luchetti; Barbara Mantovani
Journal:  J Mol Evol       Date:  2009-11-11       Impact factor: 2.395

10.  Cytogenetic diversity of SSR motifs within and between Hordeum species carrying the H genome: H. vulgare L. and H. bulbosum L.

Authors:  Alejandro Carmona; Eva Friero; Alfredo de Bustos; Nicolás Jouve; Angeles Cuadrado
Journal:  Theor Appl Genet       Date:  2012-12-15       Impact factor: 5.699

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