Impact of stainless-steel welding fumes on proteins and non-coding RNAs regulating DNA damage response in the respiratory tract of Sprague-Dawley rats

2018 ◽  
Vol 81 (24) ◽  
pp. 1231-1245 ◽  
Author(s):  
Jayaraman Krishnaraj ◽  
Abdul Basit Baba ◽  
Periasamy Viswanathan ◽  
Veeran Veeravarmal ◽  
Viswalingam Balasubramanian ◽  
...  
2017 ◽  
Vol 274 ◽  
pp. 8-19 ◽  
Author(s):  
Jayaraman Krishnaraj ◽  
Jaganathan Kowshik ◽  
Robin Sebastian ◽  
Sathees C. Raghavan ◽  
Siddavaram Nagini

2003 ◽  
Vol 24 (6) ◽  
pp. 777-785 ◽  
Author(s):  
Il Je Yu ◽  
Jung Duck Park ◽  
Eon Sub Park ◽  
Kyung Seuk Song ◽  
Kuy Tae Han ◽  
...  

PLoS ONE ◽  
2012 ◽  
Vol 7 (11) ◽  
pp. e48066 ◽  
Author(s):  
Aqian Li ◽  
Guifeng Wei ◽  
Yunfei Wang ◽  
Ying Zhou ◽  
Xian-en Zhang ◽  
...  

2003 ◽  
Vol 143 (3) ◽  
pp. 247-259 ◽  
Author(s):  
Il Je Yu ◽  
Kyung Seuk Song ◽  
Hee Kyung Chang ◽  
Jeong Hee Han ◽  
Yong Hyun Chung ◽  
...  

2017 ◽  
Vol 8 (1) ◽  
Author(s):  
Francesca Rossiello ◽  
Julio Aguado ◽  
Sara Sepe ◽  
Fabio Iannelli ◽  
Quan Nguyen ◽  
...  

Abstract The DNA damage response (DDR) is a set of cellular events that follows the generation of DNA damage. Recently, site-specific small non-coding RNAs, also termed DNA damage response RNAs (DDRNAs), have been shown to play a role in DDR signalling and DNA repair. Dysfunctional telomeres activate DDR in ageing, cancer and an increasing number of identified pathological conditions. Here we show that, in mammals, telomere dysfunction induces the transcription of telomeric DDRNAs (tDDRNAs) and their longer precursors from both DNA strands. DDR activation and maintenance at telomeres depend on the biogenesis and functions of tDDRNAs. Their functional inhibition by sequence-specific antisense oligonucleotides allows the unprecedented telomere-specific DDR inactivation in cultured cells and in vivo in mouse tissues. In summary, these results demonstrate that tDDRNAs are induced at dysfunctional telomeres and are necessary for DDR activation and they validate the viability of locus-specific DDR inhibition by targeting DDRNAs.


2009 ◽  
Vol 21 (4) ◽  
pp. 347-373 ◽  
Author(s):  
Jung-Hwa Oh ◽  
Mi-jin Yang ◽  
Young-Su Yang ◽  
Han-Jin Park ◽  
Sun Hee Heo ◽  
...  

Author(s):  
Dong Li ◽  
Ying Ge ◽  
Ze Zhao ◽  
Rui Zhu ◽  
Xiang Wang ◽  
...  

Small non-coding RNAs (ncRNAs), including microRNAs (miRNAs) and PIWI-interacting RNAs (piRNAs), play a pivotal role in biological processes. A comprehensive quantitative reference of small ncRNAs expression during development and in DNA damage response (DDR) would significantly advance our understanding of their roles. In this study, we systemically analyzed the expression profile of miRNAs and piRNAs in wild-type flies, e2f1 mutant, p53 mutant and e2f1 p53 double mutant during development and after X-ray irradiation. By using small RNA sequencing and bioinformatic analysis, we found that both miRNAs and piRNAs were expressed in a dynamic mode and formed 4 distinct clusters during development. Notably, the expression pattern of miRNAs and piRNAs was changed in e2f1 mutant at multiple developmental stages, while retained in p53 mutant, indicating a critical role of E2f1 played in mediating small ncRNAs expression. Moreover, we identified differentially expressed (DE) small ncRNAs in e2f1 mutant and p53 mutant after X-ray irradiation. Furthermore, we mapped the binding motif of E2f1 and p53 around the small ncRNAs. Our data suggested that E2f1 and p53 work differently yet coordinately to regulate small ncRNAs expression, and E2f1 may play a major role to regulate miRNAs during development and after X-ray irradiation. Collectively, our results provide comprehensive characterization of small ncRNAs, as well as the regulatory roles of E2f1 and p53 in small ncRNAs expression, during development and in DNA damage response, which reveal new insights into the small ncRNAs biology.


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