scholarly journals Faculty Opinions recommendation of Genomic stability through time despite decades of exploitation in cod on both sides of the Atlantic.

Author(s):  
Joe Hoffman
Keyword(s):  
10.2741/s379 ◽  
2013 ◽  
Vol S5 (2) ◽  
pp. 396-411 ◽  
Author(s):  
Nicolas Carlos Hoch

2010 ◽  
Vol 32 (5) ◽  
pp. 467-472
Author(s):  
Yu SUI ◽  
Yuan-Jie LI ◽  
Cai-Xia JIN ◽  
Fang XU
Keyword(s):  

1999 ◽  
Vol 5 (S2) ◽  
pp. 1286-1287
Author(s):  
Heide Schatten ◽  
Christopher N. Hueser ◽  
Amitabha Chakrabarti

The formation of abnormal mitosis associated with cancer has been intriguing for many decades. While microtubules had been the focus of previous studies, recent research has focused on centrosomes, microtubule organizing centers which organize the mitotic apparatus during cell division. During normal mitosis centrosomes form two poles but in cancer, centrosomes can form three, four, or more poles, and organize tripolar, quadripolar, and multipolar mitoses, respectively. This has severe consequences for genomic stability because chromosomes are separated unequally to three, four, or more poles. This can result in aneuploidy and gene amplifications with multiple defects in cellular regulation. It can result in malignancy that is accompanied by cell cycle imbalances and abnormal cell proliferation. While radiation and chemical agents are known to damage DNA and can lead to cell cycle abnormalities, the damage of centrosome structure leading to abnormal mitosis deserves also consideration.


PLoS Genetics ◽  
2013 ◽  
Vol 9 (2) ◽  
pp. e1003298 ◽  
Author(s):  
Wei Shi ◽  
Amanda L. Bain ◽  
Bjoern Schwer ◽  
Fares Al-Ejeh ◽  
Corey Smith ◽  
...  

Cytotherapy ◽  
2021 ◽  
Vol 23 (5) ◽  
pp. S125
Author(s):  
A. Ntai ◽  
A. La Spada ◽  
M. Valle ◽  
A. Sconda ◽  
H. Carlus-Charles ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Xiaoping Xu ◽  
Kai Ni ◽  
Yafeng He ◽  
Jianke Ren ◽  
Chongkui Sun ◽  
...  

AbstractThe Immunodeficiency Centromeric Instability Facial Anomalies (ICF) 4 syndrome is caused by mutations in LSH/HELLS, a chromatin remodeler promoting incorporation of histone variant macroH2A. Here, we demonstrate that LSH depletion results in degradation of nascent DNA at stalled replication forks and the generation of genomic instability. The protection of stalled forks is mediated by macroH2A, whose knockdown mimics LSH depletion and whose overexpression rescues nascent DNA degradation. LSH or macroH2A deficiency leads to an impairment of RAD51 loading, a factor that prevents MRE11 and EXO1 mediated nascent DNA degradation. The defect in RAD51 loading is linked to a disbalance of BRCA1 and 53BP1 accumulation at stalled forks. This is associated with perturbed histone modifications, including abnormal H4K20 methylation that is critical for BRCA1 enrichment and 53BP1 exclusion. Altogether, our results illuminate the mechanism underlying a human syndrome and reveal a critical role of LSH mediated chromatin remodeling in genomic stability.


PLoS Genetics ◽  
2010 ◽  
Vol 6 (1) ◽  
pp. e1000826 ◽  
Author(s):  
Yulong Liang ◽  
Hong Gao ◽  
Shiaw-Yih Lin ◽  
Guang Peng ◽  
Xingxu Huang ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Wendan Ren ◽  
Huitao Fan ◽  
Sara A. Grimm ◽  
Jae Jin Kim ◽  
Linhui Li ◽  
...  

AbstractDNA methylation and trimethylated histone H4 Lysine 20 (H4K20me3) constitute two important heterochromatin-enriched marks that frequently cooperate in silencing repetitive elements of the mammalian genome. However, it remains elusive how these two chromatin modifications crosstalk. Here, we report that DNA methyltransferase 1 (DNMT1) specifically ‘recognizes’ H4K20me3 via its first bromo-adjacent-homology domain (DNMT1BAH1). Engagement of DNMT1BAH1-H4K20me3 ensures heterochromatin targeting of DNMT1 and DNA methylation at LINE-1 retrotransposons, and cooperates with the previously reported readout of histone H3 tail modifications (i.e., H3K9me3 and H3 ubiquitylation) by the RFTS domain to allosterically regulate DNMT1’s activity. Interplay between RFTS and BAH1 domains of DNMT1 profoundly impacts DNA methylation at both global and focal levels and genomic resistance to radiation-induced damage. Together, our study establishes a direct link between H4K20me3 and DNA methylation, providing a mechanism in which multivalent recognition of repressive histone modifications by DNMT1 ensures appropriate DNA methylation patterning and genomic stability.


2015 ◽  
Vol 60 (1) ◽  
pp. 21-34 ◽  
Author(s):  
Seung Baek Lee ◽  
Jung Jin Kim ◽  
Hyun-Ja Nam ◽  
Bowen Gao ◽  
Ping Yin ◽  
...  
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document