change of gene structure and function by non-homologous end-joining, homologous recombination, and transposition of dna改变基因结构和功能的异源end-joining,同源重组和换位的dna.pdfVIP

  • 2
  • 0
  • 约10.71万字
  • 约 15页
  • 2017-08-31 发布于上海
  • 举报

change of gene structure and function by non-homologous end-joining, homologous recombination, and transposition of dna改变基因结构和功能的异源end-joining,同源重组和换位的dna.pdf

change of gene structure and function by non-homologous end-joining, homologous recombination, and transposition of dna改变基因结构和功能的异源end-joining,同源重组和换位的dna

Change of Gene Structure and Function by Non- Homologous End-Joining, Homologous Recombination, and Transposition of DNA Wolfgang Goettel, Joachim Messing* Waksman Institute of Microbiology, Rutgers University, Piscataway, New Jersey, United States of America Abstract An important objective in genome research is to relate genome structure to gene function. Sequence comparisons among orthologous and paralogous genes and their allelic variants can reveal sequences of functional significance. Here, we describe a 379-kb region on chromosome 1 of maize that enables us to reconstruct chromosome breakage, transposition, non-homologous end-joining, and homologous recombination events. Such a high-density composition of various mechanisms in a small chromosomal interval exemplifies the evolution of gene regulation and allelic diversity in general. It also illustrates the evolutionary pace of changes in plants, where many of the above mechanisms are of somatic origin. In contrast to animals, somatic alterations can easily be transmitted through meiosis because the germline in plants is contiguous to somatic tissue, permitting the recovery of such chromosomal rearrangements. The analyzed region contains the P1-wr allele, a variant of the genetically well-defined p1 gene, which encodes a Myb-like transcriptional activator in maize. The P1-wr allele consists of eleven nearly perfect P1-wr 12-kb repeats that are arranged in a tandem head-to-tail array. Although a technical challenge to sequence such a structure by shotgun sequencing, we overcame this problem by subcloning each repeat and ordering them based on nucleotide variations. These polymorphisms were also critical for recombination and expression analysis in presence and absence of the trans-acting epigenetic factor Uf

您可能关注的文档

文档评论(0)

1亿VIP精品文档

相关文档