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Sequential Loading of Cohesin Subunits during the First Meiotic Prophase of Grasshoppers

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dc.creator Valdeolmillos, Ana M.
dc.creator Viera, Alberto
dc.creator Page, Jesús
dc.creator Prieto, Ignacio
dc.creator Santos, Juan L.
dc.creator Parra, María Teresa
dc.creator Heck, Margarete M. S.
dc.creator Martínez-Alonso, Carlos
dc.creator Barbero, José Luis
dc.creator Suja, José A.
dc.creator Rufas, Julio S.
dc.date 2008-02-06T23:57:00Z
dc.date 2008-02-06T23:57:00Z
dc.date 2007-02-23
dc.date.accessioned 2017-01-31T01:00:00Z
dc.date.available 2017-01-31T01:00:00Z
dc.identifier PLoS Genet.; 3(2): e28 (February 2007).
dc.identifier 1553-7404
dc.identifier http://hdl.handle.net/10261/2888
dc.identifier 10.1371/journal.pgen.0030028
dc.identifier.uri http://dspace.mediu.edu.my:8181/xmlui/handle/10261/2888
dc.description A previous version of this article appeared as an Early Online Release on January 2, 2007 (doi:10.1371/journal.pgen.0030028.eor).
dc.description The cohesin complexes play a key role in chromosome segregation during both mitosis and meiosis. They establish sister chromatid cohesion between duplicating DNA molecules during S-phase, but they also have an important role during postreplicative double-strand break repair in mitosis, as well as during recombination between homologous chromosomes in meiosis. An additional function in meiosis is related to the sister kinetochore cohesion, so they can be pulled by microtubules to the same pole at anaphase I. Data about the dynamics of cohesin subunits during meiosis are scarce; therefore, it is of great interest to characterize how the formation of the cohesin complexes is achieved in order to understand the roles of the different subunits within them. We have investigated the spatio-temporal distribution of three different cohesin subunits in prophase I grasshopper spermatocytes. We found that structural maintenance of chromosome protein 3 (SMC3) appears as early as preleptotene, and its localization resembles the location of the unsynapsed axial elements, whereas radiation-sensitive mutant 21 (RAD21) (sister chromatid cohesion protein 1, SCC1) and stromal antigen protein 1 (SA1) (sister chromatid cohesion protein 3, SCC3) are not visualized until zygotene, since they are located in the synapsed regions of the bivalents. During pachytene, the distribution of the three cohesin subunits is very similar and all appear along the trajectories of the lateral elements of the autosomal synaptonemal complexes. However, whereas SMC3 also appears over the single and unsynapsed X chromosome, RAD21 and SA1 do not. We conclude that the loading of SMC3 and the non-SMC subunits, RAD21 and SA1, occurs in different steps throughout prophase I grasshopper meiosis. These results strongly suggest the participation of SMC3 in the initial cohesin axis formation as early as preleptotene, thus contributing to sister chromatid cohesion, with a later association of both RAD21 and SA1 subunits at zygotene to reinforce and stabilize the bivalent structure. Therefore, we speculate that more than one cohesin complex participates in the sister chromatid cohesion at prophase I.
dc.description This work was supported by grants BFU2005–05668-C03–01, BFU2006–06655, BFU2005–01266, BFU2005–02431, and BFU2006–04406 from Ministerio de Educación y Ciencia, España, and grants 1001160016 and 11/BCB/013 from Universidad Autónoma de Madrid and Comunidad de Madrid. The Department of Immunology and Oncology was founded and is supported by the Spanish Council for Scientific Research (CSIC).
dc.description Peer reviewed
dc.format 796561 bytes
dc.format application/pdf
dc.language eng
dc.publisher Public Library of Science
dc.relation Publisher’s version
dc.rights openAccess
dc.title Sequential Loading of Cohesin Subunits during the First Meiotic Prophase of Grasshoppers
dc.type Artículo


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