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
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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
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