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Electron tomography of mouse LINC complexes at meiotic telomere attachment sites with and without microtubules.


ABSTRACT: Telomere movements during meiotic prophase I facilitate synapsis and recombination of homologous chromosomes. Hereby, chromosome movements depend on the dynamic attachment of meiotic telomeres to the nuclear envelope and generation of forces that actively move the telomeres. In most eukaryotes, forces that move telomeres are generated in the cytoplasm by microtubule-associated motor proteins and transduced into the nucleus through the LINC complexes of the nuclear envelope. Meiotic LINC complexes, in mouse comprised of SUN1/2 and KASH5, selectively localize to the attachment sites of meiotic telomeres. For a better understanding of meiotic telomere dynamics, here we provide quantitative information of telomere attachment sites that we have generated with the aid of electron microscope tomography (EM tomography). Our data on the number, length, width, distribution and relation with microtubules of the reconstructed structures indicate that an average number of 76 LINC complexes would be required to move a telomere attachment site.

SUBMITTER: Spindler MC 

PROVIDER: S-EPMC6791847 | biostudies-other | 2019

REPOSITORIES: biostudies-other

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Electron tomography of mouse LINC complexes at meiotic telomere attachment sites with and without microtubules.

Spindler Marie-Christin MC   Redolfi Josef J   Helmprobst Frederik F   Kollmannsberger Philip P   Stigloher Christian C   Benavente Ricardo R  

Communications biology 20191014


Telomere movements during meiotic prophase I facilitate synapsis and recombination of homologous chromosomes. Hereby, chromosome movements depend on the dynamic attachment of meiotic telomeres to the nuclear envelope and generation of forces that actively move the telomeres. In most eukaryotes, forces that move telomeres are generated in the cytoplasm by microtubule-associated motor proteins and transduced into the nucleus through the LINC complexes of the nuclear envelope. Meiotic LINC complexe  ...[more]