Sororin is enriched at the central region of synapsed meiotic chromosomes

Philip W. Jordan, Craig Eyster, Jingrong Chen, Roberto J. Pezza, Susannah Rankin

Research output: Contribution to journalArticlepeer-review

5 Scopus citations


During meiotic prophase, cohesin complexes mediate cohesion between sister chromatids and promote pairing and synapsis of homologous chromosomes. Precisely how the activity of cohesin is controlled to promote these events is not fully understood. In metazoans, cohesion establishment between sister chromatids during mitotic divisions is accompanied by recruitment of the cohesion-stabilizing protein Sororin. During somatic cell division cycles, Sororin is recruited in response to DNA replication-dependent modification of the cohesin complex by ESCO acetyltransferases. How Sororin is recruited and acts in meiosis is less clear. Here, we have surveyed the chromosomal localization of Sororin and its relationship to the meiotic cohesins and other chromatin modifiers with the objective of determining how Sororin contributes to meiotic chromosome dynamics. We show that Sororin localizes to the cores of meiotic chromosomes in a manner that is dependent on synapsis and the synaptonemal complex protein SYCP1. In contrast, cohesin, with which Sororin interacts in mitotic cells, shows axial enrichment on meiotic chromosomes even in the absence of synapsis between homologs. Using high-resolution microscopy, we show that Sororin is localized to the central region of the synaptonemal complex. These results indicate that Sororin regulation during meiosis is distinct from its regulation in mitotic cells and may suggest that it interacts with a distinctly different partner to ensure proper chromosome dynamics in meiosis.

Original languageEnglish (US)
Pages (from-to)115-128
Number of pages14
JournalChromosome Research
Issue number2
StatePublished - Jun 1 2017


  • Chromosome synapsis
  • Cohesin
  • Meiosis
  • Meiotic prophase
  • Sororin

ASJC Scopus subject areas

  • Genetics


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