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Christian S Eichinger


christian.eichinger@bioch.ox.ac.uk

Journal articles

2011
2010
C S Eichinger, S Jentsch (2010)  Synaptonemal complex formation and meiotic checkpoint signaling are linked to the lateral element protein Red1   Proc Natl Acad Sci U S A 107: 25. 11370-5  
Abstract: Meiosis generates four haploid daughters from a diploid parental cell. Central steps of meiosis are the pairing and recombination of homologous chromosomes followed by their segregation in two rounds of cell division. Meiotic recombination is monitored by a specialized DNA damage checkpoint pathway and is guided by a unique chromosomal structure called synaptonemal complex (SC), but how these events are coordinated is unclear. Here, we identify the SC protein Red1 as a crucial regulator of early meiosis. Red1 interacts with two subunits of the 9-1-1 checkpoint complex via two distinct 9-1-1 subunit-specific motifs. Association of 9-1-1 with Red1 is essential not only for meiotic checkpoint activation but for SC formation. Moreover, Red1 becomes SUMO-modified, which fosters interaction of Red1 with the central SC element Zip1, thereby securing timely SC formation. Thus, Red1, in addition to its structural role in the SC, is a crucial coordinator of meiosis by coupling checkpoint signaling to SC formation.
Notes: Eichinger, Christian S xD;Jentsch, Stefan xD;Research Support, Non-U.S. Gov't xD;United States xD;Proceedings of the National Academy of Sciences of the United States of America xD;Proc Natl Acad Sci U S A. 2010 Jun 22;107(25):11370-5. Epub 2010 Jun 3.
2009
C S Eichinger, T Mizuno, K Mizuno, Y Miyake, K Yanagi, N Imamoto, F Hanaoka (2009)  Aberrant DNA polymerase alpha is excluded from the nucleus by defective import and degradation in the nucleus   J Biol Chem 284: 44. 30604-14  
Abstract: DNA polymerase alpha is essential for the onset of eukaryotic DNA replication. Its correct folding and assembly within the nuclear replication pre-initiation complex is crucial for normal cell cycle progression and genome maintenance. Due to a single point mutation in the largest DNA polymerase alpha subunit, p180, the temperature-sensitive mouse cell line tsFT20 exhibits heat-labile DNA polymerase alpha activity and S phase arrest at restrictive temperature. In this study, we show that an aberrant form of endogenous p180 in tsFT20 cells (p180(tsFT20)) is strictly localized in the cytoplasm while its wild-type counterpart enters the nucleus. Time-lapse fluorescence microscopy with enhanced green fluorescent protein-tagged or photoactivatable green fluorescent protein-tagged p180(tsFT20) variants and inhibitor analysis revealed that the exclusion of aberrant p180(tsFT20) from the nucleus is due to two distinct mechanisms: first, the inability of newly synthesized (cytoplasmic) p180(tsFT20) to enter the nucleus and second, proteasome-dependent degradation of nuclear-localized protein. The nuclear import defect seems to result from an impaired association of aberrant de novo synthesized p180(tsFT20) with the second subunit of DNA polymerase alpha, p68. In accordance, we show that RNA interference of p68 results in a decrease of the overall p180 protein level and in a specific increase of cytoplasmic localized p180 in NIH3T3 cells. Taken together, our data suggest two mechanisms that prevent the nuclear expression of aberrant DNA polymerase alpha.
Notes: Eichinger, Christian S xD;Mizuno, Takeshi xD;Mizuno, Keiko xD;Miyake, Yasuyuki xD;Yanagi, Ken-ichiro xD;Imamoto, Naoko xD;Hanaoka, Fumio xD;Research Support, Non-U.S. Gov't xD;United States xD;The Journal of biological chemistry xD;J Biol Chem. 2009 Oct 30;284(44):30604-14. Epub 2009 Sep 2.

Book chapters

2011

Masters theses

2003

PhD theses

2009

Research Fellowships

2010
2006
2004
2003
2001
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