Abstract
Background: Meiosis is a critical process in the reproduction and life cycle of flowering plants in which homologous chromosomes pair, synapse, recombine and segregate. Understanding meiosis will not only advance our knowledge of the mechanisms of genetic recombination, but also has substantial applications in crop improvement. Despite the tremendous progress in the past decade in other model organisms (e.g., Saccharomyces cerevisiae and Drosophila melanogaster), the global identification of meiotic genes in flowering plants has remained a challenge due to the lack of efficient methods to collect pure meiocytes for analyzing the temporal and spatial gene expression patterns during meiosis, and for the sensitive identification and quantitation of novel genes.Results: A high-throughput approach to identify meiosis-specific genes by combining isolated meiocytes, RNA-Seq, bioinformatic and statistical analysis pipelines was developed. By analyzing the studied genes that have a meiosis function, a pipeline for identifying meiosis-specific genes has been defined. More than 1,000 genes that are specifically or preferentially expressed in meiocytes have been identified as candidate meiosis-specific genes. A group of 55 genes that have mitochondrial genome origins and a significant number of transposable element (TE) genes (1,036) were also found to have up-regulated expression levels in meiocytes.Conclusion: These findings advance our understanding of meiotic genes, gene expression and regulation, especially the transcript profiles of MGI genes and TE genes, and provide a framework for functional analysis of genes in meiosis.
Original language | English (US) |
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Article number | 280 |
Journal | BMC plant biology |
Volume | 10 |
DOIs | |
State | Published - Dec 17 2010 |
Bibliographical note
Funding Information:We sincerely thank Dr. Blake C. Meyers, and two anonymous reviewers for comments on the manuscript, especially on TEs; Ross Peterson, Tao Li, and Duane McDowell for plant care; Dr. Gary Gardner for help installing the fluorescence microscope with digital imaging system. This project is currently sponsored by the Biotechnology Research and Development Corporation (BRDC) with the partnership of Dow AgroSciences, LLC. We also greatly appreciated the support from the Academic Health Center at the University of Minnesota and the Genome Sequencing Center at National Center for Genome Resources.