Rye (Secale cereale) supernumerary (B) chromosomes associated with heat tolerance during early stages of male sporogenesis

Ann Bot. 2017 Feb;119(3):325-337. doi: 10.1093/aob/mcw206. Epub 2016 Nov 5.

Abstract

Background and aims: Rye supernumerary (B) chromosomes have an accumulation mechanism involving the B subtelomeric domain highly enriched in D1100- and E3900-related sequences. In this work, the effects of heat stress during the early stages of male meiosis in 0B and +B plants were studied.

Methods: In-depth cytological analyses of chromatin structure and behaviour were performed on staged rye meiocytes utilizing DAPI, fluorescence in situ hybridization and 5-methylcytosine immune labelling. Quantitative real-time PCR was used to measure heat effects on the expression of the Hsp101 gene as well as the 3·9- and 2·7-kb E3900 forms in various tissues and meiotic stages.

Key results and conclusions: Quantitative real-time PCR established that heat induced equal up-regulation of the Hsp101 gene in 0B and 2B plants, with a marked peak in anthers with meiocytes staged at pachytene. Heat also resulted in significant up-regulation of E3900-related transcripts, especially at pachytene and for the truncated 2·7-kb form of E3900. Cytological heat-induced anomalies in prophase I, measured as the frequency of anomalous meiocytes, were significantly greater in 0B plants. Whereas telomeric sequences were widely distributed in a manner close to normal in the majority of 2B pachytene cells, most 0B meiocytes displayed abnormally clustered telomeres after chromosome pairing had occurred. Relevantly, bioinformatic analysis revealed a significantly high-density heat responsive cis regulatory sequence on E3900, clearly supporting stress-induced response of transcription for the truncated variant. Taken together, these results are the first indication that rye B chromosomes have implications on heat tolerance and may protect meiocytes against heat stress-induced damage.

Keywords: E3900 sequence family; Rye B chromosomes; heat responsive cis-regulatory elements; heat stress; meiotic chromosome dynamics; prophase I; transcription regulation.

MeSH terms

  • Chromosomes, Plant / genetics*
  • Chromosomes, Plant / physiology
  • Genes, Plant / genetics
  • Genes, Plant / physiology
  • In Situ Hybridization, Fluorescence
  • Meiosis / physiology
  • Real-Time Polymerase Chain Reaction
  • Reproduction / genetics
  • Reproduction / physiology
  • Secale / genetics*
  • Secale / physiology
  • Thermotolerance / genetics*
  • Thermotolerance / physiology
  • Transcription Factors / genetics
  • Transcription Factors / physiology

Substances

  • Transcription Factors