Literature DB >> 11868988

The 3' end formation in small RNAs.

Karthika Perumal1, Ram Reddy.   

Abstract

Small RNAs are a major class of RNAs along with transfer RNAs, ribosomal RNAs, and messenger RNAs. They vary in size from less than 100 nucleotides to several thousand nucleotides and have been identified and characterized both in prokaryotes and eukaryotes. Small RNAs participate in a variety of cellular functions including regulating RNA synthesis, RNA processing, guiding modifications in RNA, and in transport of proteins. Small RNAs are generated by a series of posttranscriptional processing steps following transcription. While RNA 5' end structure, 5' cap formation, and RNA processing mechanisms have been fairly well characterized, the 3' end processing is poorly understood. Recent data point to an emerging theme in small RNAs metabolism in which the 3' end processing is mediated by the exosome, a large multienzyme complex. In addition to removal of nucleotides by the exosome, there is simultaneous rebuilding of the 3' end of some small RNA by adenylation and/or uridylation. This review presents a picture of both degradative and rebuilding reactions operative on the 3' end of some small RNA molecules in prokaryotes and eukaryotes.

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Substances:

Year:  2002        PMID: 11868988      PMCID: PMC5977532     

Source DB:  PubMed          Journal:  Gene Expr        ISSN: 1052-2166


  146 in total

1.  Effect of 3' terminal adenylic acid residue on the uridylation of human small RNAs in vitro and in frog oocytes.

Authors:  Y Chen; K Sinha; K Perumal; R Reddy
Journal:  RNA       Date:  2000-09       Impact factor: 4.942

Review 2.  The biochemistry of 3'-end cleavage and polyadenylation of messenger RNA precursors.

Authors:  E Wahle; W Keller
Journal:  Annu Rev Biochem       Date:  1992       Impact factor: 23.643

3.  Sequences required for 3' end formation of human U2 small nuclear RNA.

Authors:  C Y Yuo; M Ares; A M Weiner
Journal:  Cell       Date:  1985-08       Impact factor: 41.582

4.  Polyadenylation of stable RNA precursors in vivo.

Authors:  Z Li; S Pandit; M P Deutscher
Journal:  Proc Natl Acad Sci U S A       Date:  1998-10-13       Impact factor: 11.205

5.  Ribosomal 5 S rRNA maturation in Saccharomyces cerevisiae.

Authors:  Y Lee; R N Nazar
Journal:  J Biol Chem       Date:  1997-06-13       Impact factor: 5.157

6.  Dob1p (Mtr4p) is a putative ATP-dependent RNA helicase required for the 3' end formation of 5.8S rRNA in Saccharomyces cerevisiae.

Authors:  J de la Cruz; D Kressler; D Tollervey; P Linder
Journal:  EMBO J       Date:  1998-02-16       Impact factor: 11.598

7.  Formation of the 3' end of U1 snRNA requires compatible snRNA promoter elements.

Authors:  N Hernandez; A M Weiner
Journal:  Cell       Date:  1986-10-24       Impact factor: 41.582

8.  RNase E is required for the maturation of ssrA RNA and normal ssrA RNA peptide-tagging activity.

Authors:  S Lin-Chao; C L Wei; Y T Lin
Journal:  Proc Natl Acad Sci U S A       Date:  1999-10-26       Impact factor: 11.205

9.  Precise excision of intervening sequences from precursor tRNAs by a membrane-associated yeast endonuclease.

Authors:  C L Peebles; P Gegenheimer; J Abelson
Journal:  Cell       Date:  1983-02       Impact factor: 41.582

10.  The 3' end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism.

Authors:  P Mitchell; E Petfalski; D Tollervey
Journal:  Genes Dev       Date:  1996-02-15       Impact factor: 11.361

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  15 in total

1.  Pti1p and Ref2p found in association with the mRNA 3' end formation complex direct snoRNA maturation.

Authors:  Sonia Dheur; Le Thuy Anh Vo; Florence Voisinet-Hakil; Michèle Minet; Jean-Marie Schmitter; François Lacroute; Françoise Wyers; Lionel Minvielle-Sebastia
Journal:  EMBO J       Date:  2003-06-02       Impact factor: 11.598

Review 2.  trans and cis splicing in trypanosomatids: mechanism, factors, and regulation.

Authors:  Xue-hai Liang; Asaf Haritan; Shai Uliel; Shulamit Michaeli
Journal:  Eukaryot Cell       Date:  2003-10

3.  3'-End polishing of the kinetoplastid spliced leader RNA is performed by SNIP, a 3'-->5' exonuclease with a Motley assortment of small RNA substrates.

Authors:  Gusti M Zeiner; Robert A Hitchcock; Nancy R Sturm; David A Campbell
Journal:  Mol Cell Biol       Date:  2004-12       Impact factor: 4.272

Review 4.  The exozyme model: a continuum of functionally distinct complexes.

Authors:  Daniel L Kiss; Erik D Andrulis
Journal:  RNA       Date:  2010-11-10       Impact factor: 4.942

5.  Sequence-specific RNA binding mediated by the RNase PH domain of components of the exosome.

Authors:  John R Anderson; Devi Mukherjee; Karthika Muthukumaraswamy; Karen C M Moraes; Carol J Wilusz; Jeffrey Wilusz
Journal:  RNA       Date:  2006-08-15       Impact factor: 4.942

Review 6.  Transcription termination by the eukaryotic RNA polymerase III.

Authors:  Aneeshkumar G Arimbasseri; Keshab Rijal; Richard J Maraia
Journal:  Biochim Biophys Acta       Date:  2012-10-23

7.  A novel class of developmentally regulated noncoding RNAs in Leishmania.

Authors:  Carole Dumas; Conan Chow; Michaela Müller; Barbara Papadopoulou
Journal:  Eukaryot Cell       Date:  2006-10-27

8.  Selective stabilization of mammalian microRNAs by 3' adenylation mediated by the cytoplasmic poly(A) polymerase GLD-2.

Authors:  Takayuki Katoh; Yuriko Sakaguchi; Kenjyo Miyauchi; Takeo Suzuki; Shin-Ichi Kashiwabara; Tadashi Baba; Tsutomu Suzuki
Journal:  Genes Dev       Date:  2009-02-15       Impact factor: 11.361

9.  The SNORD115 (H/MBII-52) and SNORD116 (H/MBII-85) gene clusters at the imprinted Prader-Willi locus generate canonical box C/D snoRNAs.

Authors:  Marie-Line Bortolin-Cavaillé; Jérôme Cavaillé
Journal:  Nucleic Acids Res       Date:  2012-04-11       Impact factor: 16.971

10.  Certain adenylated non-coding RNAs, including 5' leader sequences of primary microRNA transcripts, accumulate in mouse cells following depletion of the RNA helicase MTR4.

Authors:  Jane E Dorweiler; Ting Ni; Jun Zhu; Stephen H Munroe; James T Anderson
Journal:  PLoS One       Date:  2014-06-13       Impact factor: 3.240

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