Population dynamics of miniature inverted-repeat transposable elements (MITEs) in Medicago truncatula.

Miniature inverted-repeat transposable elements (MITEs) are small and high copy number transposons, related to and mobilized by some class II autonomous elements. New MITE families can be identified by computer-based mining of sequenced genomes. We describe four MITE families related to MtPH transposons mined de novo in the genome of Medicago truncatula, together with one previously described family MITRAV. Different levels of their intra-family sequence diversity and insertion polymorphism indicate that they were active at different evolutionary periods. MetMIT1 and MITRAV families were uniform in sequence and produced highly polymorphic insertion sites in 26 ecotypes representing a M. truncatula core collection. A subset of insertions was present only in the reference genome of A17 'Jemalong', suggesting that the two families might have been active in the course of domestication. In contrast, all investigated insertions of the MetMIT2 family were fixed, showing that it was not active after M. truncatula speciation. MetMIT1 elements were divided into three clusters, i.e. (I) relatively heterogenous copies fixed in the genome of M. truncatula, (II) uniform but also mostly fixed, and (III) uniform and polymorphic among the investigated accessions. It might reflect the evolutionary history of the MetMIT1 family, showing multiple bursts of activity. A number of MetMIT1 and MITRAV insertions were present within 1 kb upstream or downstream the ORF. A high proportion of insertions proximal to coding regions was unique to A17 'Jemalong'.

[1]  C Brouwer,et al.  The MITE family heartbreaker (Hbr): molecular markers in maize. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[2]  Yutaka Okumoto,et al.  Mobilization of a transposon in the rice genome , 2003, Nature.

[3]  A. Flavell,et al.  Insertional Polymorphism and Antiquity of PDR1 Retrotransposon Insertions in Pisum Species , 2005, Genetics.

[4]  Bao Liu,et al.  Mobilization of the active MITE transposons mPing and Pong in rice by introgression from wild rice (Zizania latifolia Griseb.). , 2005, Molecular biology and evolution.

[5]  J. Jurka Repbase update: a database and an electronic journal of repetitive elements. , 2000, Trends in genetics : TIG.

[6]  R. Mason-Gamer Multiple homoplasious insertions and deletions of a Triticeae (Poaceae) DNA transposon: a phylogenetic perspective , 2007, BMC Evolutionary Biology.

[7]  Bao Liu,et al.  In planta mobilization of mPing and its putative autonomous element Pong in rice by hydrostatic pressurization. , 2006, Journal of experimental botany.

[8]  T. A. Hall,et al.  BIOEDIT: A USER-FRIENDLY BIOLOGICAL SEQUENCE ALIGNMENT EDITOR AND ANALYSIS PROGRAM FOR WINDOWS 95/98/ NT , 1999 .

[9]  Sean R. Eddy,et al.  An active DNA transposon family in rice , 2003, Nature.

[10]  Slawomir Lasota,et al.  Diversity and structure of PIF/Harbinger-like elements in the genome of Medicago truncatula , 2007, BMC Genomics.

[11]  P. Simon,et al.  Diversity of DcMaster-like elements of the PIF/Harbinger superfamily in the carrot genome , 2009, Genetica.

[12]  J. Casacuberta,et al.  Plant LTR-retrotransposons and MITEs: control of transposition and impact on the evolution of plant genes and genomes. , 2003, Gene.

[13]  Guojun Yang,et al.  MAK, a computational tool kit for automated MITE analysis , 2003, Nucleic Acids Res..

[14]  Cédric Feschotte,et al.  Plant transposable elements: where genetics meets genomics , 2002, Nature Reviews Genetics.

[15]  L. Caporale The implicit genome , 2006 .

[16]  J. Thompson,et al.  The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. , 1997, Nucleic acids research.

[17]  S. Wessler,et al.  Tourist: a large family of small inverted repeat elements frequently associated with maize genes. , 1992, The Plant cell.

[18]  S. Wessler,et al.  P instability factor: An active maize transposon system associated with the amplification of Tourist-like MITEs and a new superfamily of transposases , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[19]  Cédric Feschotte,et al.  Genome-wide analysis of mariner-like transposable elements in rice reveals complex relationships with stowaway miniature inverted repeat transposable elements (MITEs). , 2003, Genetics.

[20]  C. Feschotte,et al.  DNA transposons and the evolution of eukaryotic genomes. , 2007, Annual review of genetics.

[21]  S. Wessler,et al.  Stowaway: a new family of inverted repeat elements associated with the genes of both monocotyledonous and dicotyledonous plants. , 1994, The Plant cell.

[22]  D. Grzebelus,et al.  DcMaster transposon display markers as a tool for diversity evaluation of carrot breeding materials and for hybrid seed purity testing , 2010, Journal of Applied Genetics.

[23]  S. Wessler,et al.  Evaluation of Hbr (MITE) markers for assessment of genetic relationships among maize (Zea mays L.) inbred lines , 2002, Theoretical and Applied Genetics.

[24]  D. Grzebelus Transposon insertion polymorphism as a new source of molecular markers , 2006 .

[25]  Kazuhiro Kikuchi,et al.  The plant MITE mPing is mobilized in anther culture , 2003, Nature.

[26]  S. Wessler,et al.  Recent, extensive, and preferential insertion of members of the miniature inverted-repeat transposable element family Heartbreaker into genic regions of maize. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[27]  Lukas Wagner,et al.  A Greedy Algorithm for Aligning DNA Sequences , 2000, J. Comput. Biol..

[28]  J. David,et al.  Microsatellite diversity and broad scale geographic structure in a model legume: building a set of nested core collection for studying naturally occurring variation in Medicago truncatula , 2006, BMC Plant Biology.