Identification of Epigenetic Regulators of a Transcriptionally Silenced Transgene in Maize

G3: Genes, Genomes, Genetics

Jack M. Gardiner¹  Karen M. McGinnis¹  Thelma F. Madzima¹  E. Shannon Mills¹ 

[1] Department of Biological Science, Florida State University, 319 Stadium Drive, Tallahassee, Florida 32306-4295Department of Biological Science, Florida State University, 319 Stadium Drive, Tallahassee, Florida 32306-4295Department of Biological Science, Florida State University, 319 Stadium Drive, Tallahassee, Florida 32306-4295

关键词: epigenetics;    transgene;    gene silencing;    genetic screen;   

DOI  :  10.1534/g3.111.000232

学科分类：生物科学（综合）

来源: Genetics Society of America

【 摘 要 】

Transcriptional gene silencing is a gene regulatory mechanism essential to all organisms. Many transcriptional regulatory mechanisms are associated with epigenetic modifications such as changes in chromatin structure, acetylation and methylation of core histone proteins, and DNA methylation within regulatory regions of endogenous genes and transgenes. Although several maize mutants have been identified from prior forward genetic screens for epigenetic transcriptional silencing, these screens have been far from saturated. Herein, the transcriptionally silent b1 genomic transgene (BTG-silent), a stable, epigenetically silenced transgene in Zea mays (maize), is demonstrated to be an effective phenotype for a forward genetic screen. When the transgene is reactivated, a dark purple plant phenotype is evident because the B1 transcription factor activates anthocyanin biosynthesis, making loss of silencing mutants easy to identify. Using BTG-silent, ten new putative mutants were identified and named transgene reactivated1 through 11 (tgr1-6 and tgr8-11). Three of these mutants have been examined in more detail, and molecular and genetic assays demonstrated that these mutants have both distinct and overlapping phenotypes with previously identified maize mutants that relieve epigenetic transcriptional silencing. Linkage analysis suggests that tgr2 and tgr3 do not correspond to a mutation at previously identified maize loci resulting from other forward genetic screens, while tgr1 shows linkage to a characterized gene. These results suggest that the mutants are a valuable resource for future studies because some of the mutants are likely to reveal genes that encode products required for epigenetic gene regulation in maize but are not currently represented by sequenced mutations.

【 授权许可】

Unknown