학술논문

Molecular organization of mammalian meiotic chromosome axis revealed by expansion STORM microscopy
Document Type
article
Source
Proceedings of the National Academy of Sciences of the United States of America. 116(37)
Subject
Genetics
Underpinning research
1.1 Normal biological development and functioning
Generic health relevance
Animals
Cell Cycle Proteins
Chromosomes
Mammalian
DNA-Binding Proteins
Male
Mammals
Meiosis
Mice
Microscopy
Spermatocytes
Staining and Labeling
Synaptonemal Complex
synaptonemal complex
meiosis
chromosome axis
expansion microscopy
STORM
Language
Abstract
During prophase I of meiosis, chromosomes become organized as loop arrays around the proteinaceous chromosome axis. As homologous chromosomes physically pair and recombine, the chromosome axis is integrated into the tripartite synaptonemal complex (SC) as this structure's lateral elements (LEs). While the components of the mammalian chromosome axis/LE-including meiosis-specific cohesin complexes, the axial element proteins SYCP3 and SYCP2, and the HORMA domain proteins HORMAD1 and HORMAD2-are known, the molecular organization of these components within the axis is poorly understood. Here, using expansion microscopy coupled with 2-color stochastic optical reconstruction microscopy (STORM) imaging (ExSTORM), we address these issues in mouse spermatocytes at a resolution of 10 to 20 nm. Our data show that SYCP3 and the SYCP2 C terminus, which are known to form filaments in vitro, form a compact core around which cohesin complexes, HORMADs, and the N terminus of SYCP2 are arrayed. Overall, our study provides a detailed structural view of the meiotic chromosome axis, a key organizational and regulatory component of meiotic chromosomes.