The Synaptonemal Complex Protein SCP3 Can Form Multistranded, Cross-striated Fibers In Vivo |
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| Authors: | Li Yuan, Jeanette Pelttari, Eva Brundell, Birgitta Bj rkroth, Jian Zhao, Jian-Guo Liu, Hjalmar Brismar, Bertil Daneholt, Christer H g |
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| Affiliation: | Li Yuan, Jeanette Pelttari, Eva Brundell, Birgitta Björkroth, Jian Zhao, Jian-Guo Liu, Hjalmar Brismar, Bertil Daneholt, and Christer Höög |
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| Abstract: | The synaptonemal complex protein SCP3 is part of the lateral element of the synaptonemal complex, a meiosis-specific protein structure essential for synapsis of homologous chromosomes. We have investigated the fiber-forming properties of SCP3 to elucidate its role in the synaptonemal complex. By synthesis of SCP3 in cultured somatic cells, it has been shown that SCP3 can self-assemble into thick fibers and that this process requires the COOH-terminal coiled coil domain of SCP3, as well as the NH2-terminal nonhelical domain. We have further analyzed the thick SCP3 fibers by transmission electron microscopy and immunoelectron microscopy. We found that the fibers display a transversal striation with a periodicity of ~20 nm and consist of a large number of closely associated, thin fibers, 5–10 nm in diameter. These features suggest that the SCP3 fibers are structurally related to intermediate filaments. It is known that in some species the lateral elements of the synaptonemal complex show a highly ordered striated structure resembling that of the SCP3 fibers. We propose that SCP3 fibers constitute the core of the lateral elements of the synaptonemal complex and function as a molecular framework to which other proteins attach, regulating DNA binding to the chromatid axis, sister chromatid cohesion, synapsis, and recombination. |
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| Keywords: | meiosis cohesion lateral element chromosomes recombination |
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