Science Current Events | Science News | Brightsurf.com
 
Email a Friend Send to a friend
Printer Friendly Print Researchers discover RNA repair system in bacteria

Researchers discover RNA repair system in bacteria

October 13, 2009

In new papers appearing this month in Science and the Proceedings of the National Academy of Sciences, University of Illinois biochemistry professor Raven H. Huang and his colleagues describe the first RNA repair system to be discovered in bacteria. This is only the second RNA repair system discovered to date (with two proteins from T4 phage, a virus that attacks bacteria, as the first).

The novelty of the newly discovered bacterial RNA repair system is that, before the damaged RNA is sealed, a methyl group is added to the two-prime hydroxyl group at the cleavage site of the damaged RNA, making it impossible to cleave the site again. Thus, the repaired RNA is "better than new."




This discovery has implications for protecting cells against ribotoxins, a class of toxins that kills cells by cleaving essential RNAs involved in protein translation. Because the enzyme responsible for methylation in the newly-discovered RNA repair system is the Hen1 homolog in bacteria, the finding has also implications for the understanding of RNA interference and gene expression in plants, animals, and other eukaryotes. The eukaryotic Hen1 is one of three enzymes (along with Dicer and Argonaute) essential for the generation of small noncoding RNAs of 19-30 nucleotides in RNA interference.

While the Science paper describes the mechanism of the entire RNA repair process, the article in PNAS focuses on the chemistry of the methylation reaction, specifically the crystal structure of the methyltransferase domain of bacterial Hen1. Because the eukaryotic Hen1 carries out the same chemical reaction, the study should further understanding of RNA interference in eukaryotic organisms.

"Hen1 is one of three essential enzymes in generating small noncoding RNAs for RNA interference in eukaryotes," Huang said. "We found out that Hen1 homologs exist in bacteria, but bacteria have no RNA interference. Therefore, we were very curious to find out what bacterial Hen1 is used for."

"Our studies demonstrated that bacterial Hen1 carries out the same chemical reaction as its counterpart in eukaryotes, which was not surprising," he said. "What surprised us was that, instead of involvement in RNA interference, the bacterial Hen1 is part of a RNA repair and modification system. And Hen1 is responsible for producing the repaired RNA that is 'better than new.'"

University of Illinois at Urbana-Champaign




More RNA Repair Current Events and RNA Repair News Articles
Alkylation damage in DNA and RNA-repair mechanisms and medical significance [An article from: DNA Repair]

Alkylation damage in DNA and RNA-repair mechanisms and medical significance [An article from: DNA Repair]
by F. Drablos (Author), E. Feyzi (Author), P.A. Aas (Author), C.B. Vaagbo (Author), Kavli (Author)

This digital document is a journal article from DNA Repair, published by Elsevier in 2004. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

Description:
Alkylation lesions in DNA and RNA result from endogenous compounds, environmental agents and alkylating drugs. Simple methylating agents, e.g. methylnitrosourea, tobacco-specific nitrosamines and drugs like temozolomide or streptozotocin, form adducts at N- and O-atoms in DNA bases. These lesions are mainly repaired by direct base repair, base excision repair, and to some extent by nucleotide excision repair (NER). The identified carcinogenicity of O^6-methylguanine (O^6-meG) is largely caused by its miscoding properties....

Lumina Health Cellfood RNA DNA Cell Regneration Formula

Lumina Health Cellfood RNA DNA Cell Regneration Formula
by Lumina Health

Cellfood DNARNA Cell Regeneration Formula is one of the most rejuvenating, immunity- enhancing, and tissue-supporting formulas ever developed. It is a proprietary blend of nucleic acid bases (the essential building blocks of DNA and RNA), methyl groups (which are considered by many scientific researchers to be the prime regulators and programmers of the aging process), ATP (the fundamental energy'currency' of the human body) and the original Cellfood formula. In Cellfood DNARNA, the life- and longevity-enhancing effects of these four special components have been combined for the very first time. And, it's been formulated in a spray, boosted with the remarkable Cellfood delivery system, and laser enhanced all combining for optimal absorption and assimilation. Advantages of Oral Spray...

Effect of 8-oxoguanine on transcription elongation by T7 RNA polymerase and mammalian RNA polymerase II [An article from: DNA Repair]

Effect of 8-oxoguanine on transcription elongation by T7 RNA polymerase and mammalian RNA polymerase II [An article from: DNA Repair]
by S. Tornaletti (Author), L.S. Maeda (Author), R.D. Kolodner (Author), Hanawalt (Author)

This digital document is a journal article from DNA Repair, published by Elsevier in 2004. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

Description:
8-Oxoguanine (8-oxoG) is a major oxidative lesion produced in DNA by normal cellular metabolism or after exposure to exogenous sources such as ionizing radiation. Persistence of this lesion in DNA causes G to T transversions, with deleterious consequences for the cell. As a result, several repair processes have evolved to remove this lesion from the genome. It has been reported that 8-oxoG is subject to transcription-coupled repair (TCR), a process dedicated to removal of lesions from transcribed strands of expressed...

Comparative TFIIS-mediated transcript cleavage by mammalian RNA polymerase II arrested at a lesion in different transcription systems [An article from: DNA Repair]

Comparative TFIIS-mediated transcript cleavage by mammalian RNA polymerase II arrested at a lesion in different transcription systems [An article from: DNA Repair]
by V.S. Kalogeraki (Author), S. Tornaletti (Author), P.K. Cooper (Author), Hanaw (Author)

This digital document is a journal article from DNA Repair, published by Elsevier in . The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

Description:
Upon prolonged arrest at a cyclobutane pyrimidine dimer (CPD), RNAPII can reverse-translocate, misaligning the 3'-end of the RNA from its active site. Transcription factor SII (TFIIS) is required for cleavage of the disengaged 3'-end and restoration of its correct positioning. We have previously shown in vitro that when RNAPII is arrested at a CPD, TFIIS-induced cleavage results in shortened transcripts. Here, we hypothesized that the pattern of transcript cleavage does not depend solely upon TFIIS itself, but also on some...

The Enzymes. Volume X Protein Synthesis DNA Synthesis and Repair RNA Synthesis Energy-Linked At Pases Synthetases. Third Edition

The Enzymes. Volume X Protein Synthesis DNA Synthesis and Repair RNA Synthesis Energy-Linked At Pases Synthetases. Third Edition
by Paul D. Boyer (Editor)



'Knock down' of DNA polymerase @b by RNA interference: recapitulation of null phenotype [An article from: DNA Repair]

'Knock down' of DNA polymerase @b by RNA interference: recapitulation of null phenotype [An article from: DNA Repair]
by Y.Y. Polosina (Author), T.A. Rosenquist (Author), A.P. Grollman (Author), Mil (Author)

This digital document is a journal article from DNA Repair, published by Elsevier in 2004. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

Description:
DNA polymerase @b (pol @b) is the major DNA polymerase involved in the base excision repair (BER) pathway in mammalian cells and, as a consequence, BER is severely compromised in cells lacking pol @b. Pol @b null (-/-) mouse embryos are not viable and pol @b null cells are hypersensitive to alkylating agents. Using RNA interference (RNAi) technology in mouse cells, we have reduced the pol @b protein and mRNA to undetectable levels. Pol @b knockdown cell lines display a pattern of hypersensitivity to DNA damaging agents...

The ATM-related kinase, hSMG-1, bridges genome and RNA surveillance pathways [An article from: DNA Repair]

The ATM-related kinase, hSMG-1, bridges genome and RNA surveillance pathways [An article from: DNA Repair]
by R.T. Abraham (Author)

This digital document is a journal article from DNA Repair, published by Elsevier in 2004. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

Description:
Recent studies have identified, hSMG-1 as the newest member of the phosphoinositide 3-kinase(PI3-kinase)-related kinase (PIKK) family. The protein kinase activity of hSMG-1 resembles that of the related PIKK, ATM, both in terms of substrate specificity and its sensitivity to inhibition by the fungal metabolite wortmannin. hSMG-1 is the ortholog of a Caenorhabditis elegans protein, CeSMG-1, which has been genetically linked to a critical mRNA surveillance pathway termed nonsense-mediated decay (NMD). The function of NMD is...

New insights for understanding the transcription-coupled repair pathway [An article from: DNA Repair]

New insights for understanding the transcription-coupled repair pathway [An article from: DNA Repair]
by A. Sarasin (Author), A. Stary (Author)

This digital document is a journal article from DNA Repair, published by Elsevier in 2007. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

Description:
Transcription-coupled repair (TCR) is a sub-pathway of nucleotide excision repair (NER) able to remove bulky DNA lesions located on the transcribed strands of active genes more rapidly than those located on the non-transcribed genomic DNA. Two recently published reports try to dissect the molecular mechanisms of TCR using simplified in vitro assays. A third report shows in vivo data that confirmed the in vitro ones and extends them to the role of other TCR factors such as those involved in chromatin remodeling. These...

The irresistible resistance of nonsense: Evolutionary adaptation of termination codons to minimize the effects of common DNA damage [An article from: DNA Repair]

The irresistible resistance of nonsense: Evolutionary adaptation of termination codons to minimize the effects of common DNA damage [An article from: DNA Repair]
by D.K. Orren (Author)

This digital document is a journal article from DNA Repair, published by Elsevier in . The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

Description:


Computational analyses show A-to-G mutations correlate with nascent mRNA hairpins at somatic hypermutation hotspots [An article from: DNA Repair]

Computational analyses show A-to-G mutations correlate with nascent mRNA hairpins at somatic hypermutation hotspots [An article from: DNA Repair]
by E.J. Steele (Author), R.A. Lindley (Author), J. Wen (Author), G.F. Weiller (Author)

This digital document is a journal article from DNA Repair, published by Elsevier in 2006. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

Description:
Activation-induced cytidine deaminase (AID) initiates Phase I somatic hypermutation (SHM) of antibody genes by deaminating deoxy-cytosine to deoxy-uracil (C-to-U). These lesions trigger Phase II, a poorly understood process of error-prone repair targeting A-T pairs by DNA polymerase @h (Pol @h). Since Pol @h is also a reverse transcriptase, Phase II could involve copying off RNA as well as DNA templates. We explore this idea further since in an RNA-based pathway it is conceivable that adenosine-to-inosine (A-to-I) RNA...

© 2009 BrightSurf.com