Essential molecular functions associated with the circular code evolution

2010 ◽  
Vol 264 (2) ◽  
pp. 613-622 ◽  
Author(s):  
Ahmed Ahmed ◽  
Gabriel Frey ◽  
Christian J. Michel
Biosystems ◽  
2021 ◽  
pp. 104431
Author(s):  
Christian J. Michel
Keyword(s):  

2011 ◽  
Vol 46 (2) ◽  
pp. 123-126
Author(s):  
Thomas Würthinger ◽  
Walter Binder ◽  
Danilo Ansaloni ◽  
Philippe Moret ◽  
Hanspeter Mössenböck

Author(s):  
M.C. Wang ◽  
H.F. Tu ◽  
K.W. Chang ◽  
S.C. Lin ◽  
L.Y. Yeh ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
H. Busra Cagirici ◽  
Hikmet Budak ◽  
Taner Z. Sen

AbstractG-quadruplexes (G4s) are four-stranded nucleic acid structures with closely spaced guanine bases forming square planar G-quartets. Aberrant formation of G4 structures has been associated with genomic instability. However, most plant species are lacking comprehensive studies of G4 motifs. In this study, genome-wide identification of G4 motifs in barley was performed, followed by a comparison of genomic distribution and molecular functions to other monocot species, such as wheat, maize, and rice. Similar to the reports on human and some plants like wheat, G4 motifs peaked around the 5′ untranslated region (5′ UTR), the first coding domain sequence, and the first intron start sites on antisense strands. Our comparative analyses in human, Arabidopsis, maize, rice, and sorghum demonstrated that the peak points could be erroneously merged into a single peak when large window sizes are used. We also showed that the G4 distributions around genic regions are relatively similar in the species studied, except in the case of Arabidopsis. G4 containing genes in monocots showed conserved molecular functions for transcription initiation and hydrolase activity. Additionally, we provided examples of imperfect G4 motifs.


Author(s):  
Kazuki Kojima ◽  
Hidenori Ichijo ◽  
Isao Naguro

Summary VCells are constantly exposed to various types of stress, and disruption of the proper response lead to a variety of diseases. Among them, inflammation and apoptosis are important examples of critical responses and should be tightly regulated, as inappropriate control of these responses is detrimental to the organism. In several disease states, these responses are abnormally regulated, with adverse effects. Apoptosis signal-regulating kinase (ASK) family members are stress-responsive kinases that regulate inflammation and apoptosis after a variety of stimuli, such as oxidative stress and endoplasmic reticulum (ER) stress. In this review, we summarize recent reports on the ASK family in terms of their involvement in inflammatory diseases, focusing on upstream stimuli that regulate ASK family members.


Author(s):  
Shaohui Chen ◽  
Xiangyang Deng ◽  
Hansong Sheng ◽  
Yuxi Rong ◽  
Yanhao Zheng ◽  
...  

2011 ◽  
Vol 19 (21) ◽  
pp. 20580 ◽  
Author(s):  
Xihua Zou ◽  
Wei Pan ◽  
Bin Luo ◽  
Lianshan Yan ◽  
Yushi Jiang

2002 ◽  
Vol 13 (9) ◽  
pp. 3029-3041 ◽  
Author(s):  
Cheryl D. Warren ◽  
D. Michelle Brady ◽  
Raymond C. Johnston ◽  
Joseph S. Hanna ◽  
Kevin G. Hardwick ◽  
...  

The spindle checkpoint plays a central role in the fidelity of chromosome transmission by ensuring that anaphase is initiated only after kinetochore-microtubule associations of all sister chromatid pairs are complete. In this study, we find that known spindle checkpoint proteins do not contribute equally to chromosome segregation fidelity in Saccharomyces cerevisiae. Loss of Bub1 or Bub3 protein elicits the largest effect. Analysis of Bub1p reveals the presence of two molecular functions. An N-terminal 608-amino acid (nonkinase) portion of the protein supports robust checkpoint activity, and, as expected, contributes to chromosome segregation. A C-terminal kinase-encoding segment independently contributes to chromosome segregation through an unknown mechanism. Both molecular functions depend on association with Bub3p. A 156-amino acid fragment of Bub1p functions in Bub3p binding and in kinetochore localization by one-hybrid assay. An adjacent segment is required for Mad1p binding, detected by deletion analysis and coimmunoprecipitation. Finally, overexpression of wild-type BUB1 or MAD3 genes leads to chromosome instability. Analysis of this activity indicates that the Bub3p-binding domain of Bub1p contributes to this phenotype through disruption of checkpoint activity as well as through introduction of kinetochore or spindle damage.


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