Ending the message: poly(A) signals then and now.

Polyadenylation [poly(A)] signals (PAS) are a defining feature of eukaryotic protein-coding genes. The central sequence motif AAUAAA was identified in the mid-1970s and subsequently shown to require flanking, auxiliary elements for both 3'-end cleavage and polyadenylation of premessenger RNA (pre-mRNA) as well as to promote downstream transcriptional termination. More recent genomic analysis has established the generality of the PAS for eukaryotic mRNA. Evidence for the mechanism of mRNA 3'-end formation is outlined, as is the way this RNA processing reaction communicates with RNA polymerase II to terminate transcription. The widespread phenomenon of alternative poly(A) site usage and how this interrelates with pre-mRNA splicing is then reviewed. This shows that gene expression can be drastically affected by how the message is ended. A central theme of this review is that while genomic analysis provides generality for the importance of PAS selection, detailed mechanistic understanding still requires the direct analysis of specific genes by genetic and biochemical approaches.

[1]  J. Manley,et al.  Transcriptional activators enhance polyadenylation of mRNA precursors , 2011, RNA biology.

[2]  Konstantina Skourti-Stathaki,et al.  Human Senataxin Resolves RNA/DNA Hybrids Formed at Transcriptional Pause Sites to Promote Xrn2-Dependent Termination , 2011, Molecular cell.

[3]  C. Sunkel,et al.  RNA polymerase II kinetics in polo polyadenylation signal selection , 2011, The EMBO journal.

[4]  C. Moore,et al.  Unravelling the means to an end: RNA polymerase II transcription termination , 2011, Nature Reviews Molecular Cell Biology.

[5]  Chong-Jian Chen,et al.  Differential genome-wide profiling of tandem 3' UTRs among human breast cancer and normal cells by high-throughput sequencing. , 2011, Genome research.

[6]  L. Steinmetz,et al.  Yeast Sen1 Helicase Protects the Genome from Transcription-Associated Instability , 2011, Molecular cell.

[7]  D. Bartel,et al.  Formation, Regulation and Evolution of Caenorhabditis elegans 3′UTRs , 2010, Nature.

[8]  C. Lutz,et al.  Alternative mRNA polyadenylation in eukaryotes: an effective regulator of gene expression , 2011, Wiley interdisciplinary reviews. RNA.

[9]  P. Kapranov,et al.  Comprehensive Polyadenylation Site Maps in Yeast and Human Reveal Pervasive Alternative Polyadenylation , 2010, Cell.

[10]  Jørgen Kjems,et al.  Crosstalk between mRNA 3' end processing and transcription initiation. , 2010, Molecular cell.

[11]  Larry N. Singh,et al.  U1 snRNP protects pre-mRNAs from premature cleavage and polyadenylation , 2010, Nature.

[12]  Shimyn Slomovic,et al.  Addition of poly(A) and poly(A)-rich tails during RNA degradation in the cytoplasm of human cells , 2010, Proceedings of the National Academy of Sciences.

[13]  Bin Tian,et al.  A functional human Poly(A) site requires only a potent DSE and an A-rich upstream sequence , 2010, The EMBO journal.

[14]  David Tollervey,et al.  Apparent Non-Canonical Trans-Splicing Is Generated by Reverse Transcriptase In Vitro , 2010, PloS one.

[15]  S. Vagner,et al.  Molecular mechanisms of eukaryotic pre-mRNA 3′ end processing regulation , 2009, Nucleic acids research.

[16]  J. Manley,et al.  Mechanisms of alternative splicing regulation: insights from molecular and genomics approaches , 2009, Nature Reviews Molecular Cell Biology.

[17]  Jeffrey G. Reifenberger,et al.  Direct RNA sequencing , 2009, Nature.

[18]  Manuel de la Mata,et al.  DNA Damage Regulates Alternative Splicing through Inhibition of RNA Polymerase II Elongation , 2009, Cell.

[19]  A. Furger,et al.  Regulation of transcription termination in the nematode Caenorhabditis elegans , 2009, Nucleic acids research.

[20]  C. Milcarek,et al.  Transcription elongation factor ELL2 directs immunoglobulin secretion in plasma cells by stimulating altered RNA processing , 2009, Nature Immunology.

[21]  C. Mayr,et al.  Widespread Shortening of 3′UTRs by Alternative Cleavage and Polyadenylation Activates Oncogenes in Cancer Cells , 2009, Cell.

[22]  Patricia Richard,et al.  Transcription termination by nuclear RNA polymerases. , 2009, Genes & development.

[23]  W. Marzluff,et al.  A core complex of CPSF73, CPSF100, and Symplekin may form two different cleavage factors for processing of poly(A) and histone mRNAs. , 2009, Molecular cell.

[24]  B. Tian,et al.  Progressive lengthening of 3′ untranslated regions of mRNAs by alternative polyadenylation during mouse embryonic development , 2009, Proceedings of the National Academy of Sciences.

[25]  N. Proudfoot,et al.  Transcriptional Termination Enhances Protein Expression in Human Cells , 2009, Molecular cell.

[26]  D. Bartel MicroRNAs: Target Recognition and Regulatory Functions , 2009, Cell.

[27]  E. Wagner,et al.  Metabolism and regulation of canonical histone mRNAs: life without a poly(A) tail , 2008, Nature Reviews Genetics.

[28]  Eric T. Wang,et al.  Alternative Isoform Regulation in Human Tissue Transcriptomes , 2008, Nature.

[29]  T. Jensen,et al.  The exosome: a multipurpose RNA-decay machine. , 2008, Trends in biochemical sciences.

[30]  J. Steitz,et al.  Conserved motifs in both CPSF73 and CPSF100 are required to assemble the active endonuclease for histone mRNA 3′‐end maturation , 2008, EMBO reports.

[31]  P. Sharp,et al.  Proliferating Cells Express mRNAs with Shortened 3' Untranslated Regions and Fewer MicroRNA Target Sites , 2008, Science.

[32]  N. Proudfoot,et al.  Molecular Dissection of Mammalian RNA Polymerase II Transcriptional Termination , 2008, Molecular cell.

[33]  M. Hentze,et al.  3′ end mRNA processing: molecular mechanisms and implications for health and disease , 2008, The EMBO journal.

[34]  M. Giacca,et al.  Transcription-Dependent Gene Looping of the HIV-1 Provirus Is Dictated by Recognition of Pre-mRNA Processing Signals , 2008, Molecular cell.

[35]  D. Bentley,et al.  RNA polymerase II pauses and associates with pre-mRNA processing factors at both ends of genes , 2008, Nature Structural &Molecular Biology.

[36]  L. Tong,et al.  Protein factors in pre-mRNA 3′-end processing , 2008, Cellular and Molecular Life Sciences.

[37]  P. Bork,et al.  Splicing factors stimulate polyadenylation via USEs at non‐canonical 3′ end formation signals , 2007, The EMBO journal.

[38]  Z. Dominski Nucleases of the Metallo-β-lactamase Family and Their Role in DNA and RNA Metabolism , 2007, Critical reviews in biochemistry and molecular biology.

[39]  A. Furger,et al.  Two G-Rich Regulatory Elements Located Adjacent to and 440 Nucleotides Downstream of the Core Poly(A) Site of the Intronless Melanocortin Receptor 1 Gene Are Critical for Efficient 3′ End Processing , 2006, Molecular and Cellular Biology.

[40]  L. Tong,et al.  Polyadenylation factor CPSF-73 is the pre-mRNA 3'-end-processing endonuclease , 2006, Nature.

[41]  Hanno Langen,et al.  Direct interactions between subunits of CPSF and the U2 snRNP contribute to the coupling of pre-mRNA 3' end processing and splicing. , 2006, Molecular cell.

[42]  N. Proudfoot,et al.  Pause Sites Promote Transcriptional Termination of Mammalian RNA Polymerase II , 2006, Molecular and Cellular Biology.

[43]  N. Proudfoot,et al.  Adenylation and exosome-mediated degradation of cotranscriptionally cleaved pre-messenger RNA in human cells. , 2006, Molecular cell.

[44]  J. Steitz,et al.  Symplekin and multiple other polyadenylation factors participate in 3'-end maturation of histone mRNAs. , 2005, Genes & development.

[45]  Z. Dominski,et al.  The Polyadenylation Factor CPSF-73 Is Involved in Histone-Pre-mRNA Processing , 2005, Cell.

[46]  Donglin Liu,et al.  BIOINFORMATICS APPLICATIONS NOTE Databases and ontologies PACdb: PolyA Cleavage Site and 3 ′-UTR Database , 2022 .

[47]  M. Moore From Birth to Death: The Complex Lives of Eukaryotic mRNAs , 2005, Science.

[48]  T. Blumenthal Trans-splicing and operons. , 2005, WormBook : the online review of C. elegans biology.

[49]  K. Venkataraman,et al.  Analysis of a noncanonical poly(A) site reveals a tripartite mechanism for vertebrate poly(A) site recognition. , 2005, Genes & development.

[50]  Daniel St Johnston,et al.  Moving messages: the intracellular localization of mRNAs , 2005, Nature Reviews Molecular Cell Biology.

[51]  N. Proudfoot,et al.  Strong Polyadenylation and Weak Pausing Combine To Cause Efficient Termination of Transcription in the Human Gγ-Globin Gene , 2005, Molecular and Cellular Biology.

[52]  Bin Tian,et al.  A large-scale analysis of mRNA polyadenylation of human and mouse genes , 2005, Nucleic acids research.

[53]  N. Proudfoot,et al.  Human 5′ → 3′ exonuclease Xrn2 promotes transcription termination at co-transcriptional cleavage sites , 2004, Nature.

[54]  N. Krogan,et al.  The yeast Rat1 exonuclease promotes transcription termination by RNA polymerase II , 2004, Nature.

[55]  Antonin Morillon,et al.  Gene loops juxtapose promoters and terminators in yeast , 2004, Nature Genetics.

[56]  Anton Meinhart,et al.  Recognition of RNA polymerase II carboxy-terminal domain by 3′-RNA-processing factors , 2004, Nature.

[57]  Nick Proudfoot,et al.  New perspectives on connecting messenger RNA 3' end formation to transcription. , 2004, Current opinion in cell biology.

[58]  K. Ryan,et al.  Evidence that polyadenylation factor CPSF-73 is the mRNA 3' processing endonuclease. , 2004, RNA.

[59]  J. Castle,et al.  Genome-Wide Survey of Human Alternative Pre-mRNA Splicing with Exon Junction Microarrays , 2003, Science.

[60]  D. Black Mechanisms of alternative pre-messenger RNA splicing. , 2003, Annual review of biochemistry.

[61]  C. Denis,et al.  In Vivo Evidence that Defects in the Transcriptional Elongation Factors RPB2, TFIIS, and SPT5 Enhance Upstream Poly(A) Site Utilization , 2003, Molecular and Cellular Biology.

[62]  A. Kornblihtt,et al.  A slow RNA polymerase II affects alternative splicing in vivo. , 2003, Molecular cell.

[63]  J. Prieto,et al.  Inhibiting expression of specific genes in mammalian cells with 5′ end-mutated U1 small nuclear RNAs targeted to terminal exons of pre-mRNA , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[64]  D. Gautheret,et al.  Sequence determinants in human polyadenylation site selection , 2003, BMC Genomics.

[65]  D. Licatalosi,et al.  Functional interaction of yeast pre-mRNA 3' end processing factors with RNA polymerase II. , 2002, Molecular cell.

[66]  J. Rowley,et al.  Oligo(dT) primer generates a high frequency of truncated cDNAs through internal poly(A) priming during reverse transcription , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[67]  A. Furger,et al.  Integrating mRNA Processing with Transcription , 2002, Cell.

[68]  M. Edmonds,et al.  A history of poly A sequences: from formation to factors to function. , 2002, Progress in nucleic acid research and molecular biology.

[69]  Matthias W. Hentze,et al.  Increased efficiency of mRNA 3′ end formation: a new genetic mechanism contributing to hereditary thrombophilia , 2001, Nature Genetics.

[70]  N. Proudfoot,et al.  Multiple Transcript Cleavage Precedes Polymerase Release in Termination by RNA Polymerase II , 2001, Cell.

[71]  N. Proudfoot,et al.  Recruitment of a Basal Polyadenylation Factor by the Upstream Sequence Element of the Human Lamin B2 Polyadenylation Signal , 2000, Molecular and Cellular Biology.

[72]  I. Mattaj,et al.  The carboxyl terminus of vertebrate poly(A) polymerase interacts with U2AF 65 to couple 3'-end processing and splicing. , 2000, Genes & development.

[73]  A. Kornblihtt,et al.  Coupling of transcription with alternative splicing: RNA pol II promoters modulate SF2/ASF and 9G8 effects on an exonic splicing enhancer. , 1999, Molecular cell.

[74]  Jing Zhao,et al.  Formation of mRNA 3′ Ends in Eukaryotes: Mechanism, Regulation, and Interrelationships with Other Steps in mRNA Synthesis , 1999, Microbiology and Molecular Biology Reviews.

[75]  N. Proudfoot,et al.  Terminal exon definition occurs cotranscriptionally and promotes termination of RNA polymerase II. , 1999, Molecular cell.

[76]  C R Cantor,et al.  Genomic detection of new yeast pre-mRNA 3'-end-processing signals. , 1999, Nucleic acids research.

[77]  J. Manley,et al.  Levels of polyadenylation factor CstF-64 control IgM heavy chain mRNA accumulation and other events associated with B cell differentiation. , 1998, Molecular cell.

[78]  G. C. Roberts,et al.  Co-transcriptional commitment to alternative splice site selection. , 1998, Nucleic acids research.

[79]  J. Manley,et al.  RNA polymerase II is an essential mRNA polyadenylation factor , 1998, Nature.

[80]  L. Minvielle-Sebastia,et al.  Coupling termination of transcription to messenger RNA maturation in yeast. , 1998, Science.

[81]  I. Mattaj,et al.  U1 snRNP inhibits pre-mRNA polyadenylation through a direct interaction between U1 70K and poly(A) polymerase. , 1998, Molecular cell.

[82]  J. Manley,et al.  Mechanism and regulation of mRNA polyadenylation. , 1997, Genes & development.

[83]  J. Dantonel,et al.  Transcription factor TFIID recruits factor CPSF for formation of 3′ end of mRNA , 1997, Nature.

[84]  N. Proudfoot,et al.  The HIV‐1 5′ LTR poly(A) site is inactivated by U1 snRNP interaction with the downstream major splice donor site , 1997, The EMBO journal.

[85]  G. Edwalds-Gilbert,et al.  Alternative poly(A) site selection in complex transcription units: means to an end? , 1997, Nucleic acids research.

[86]  M. Wickens,et al.  The C-terminal domain of RNA polymerase II couples mRNA processing to transcription , 1997, Nature.

[87]  J. Manley,et al.  The Polyadenylation Factor CstF-64 Regulates Alternative Processing of IgM Heavy Chain Pre-mRNA during B Cell Differentiation , 1996, Cell.

[88]  N. Proudfoot,et al.  Poly(A) site selection in the HIV-1 provirus: inhibition of promoter-proximal polyadenylation by the downstream major splice donor site. , 1995, Genes & development.

[89]  M. Wollerton,et al.  Upstream sequence elements enhance poly(A) site efficiency of the C2 complement gene and are phylogenetically conserved. , 1995, The EMBO journal.

[90]  J. Wilusz,et al.  Cleavage site determinants in the mammalian polyadenylation signal. , 1995, Nucleic acids research.

[91]  C. Baker,et al.  Sequences homologous to 5' splice sites are required for the inhibitory activity of papillomavirus late 3' untranslated regions , 1994, Molecular and cellular biology.

[92]  Susan M. Berget,et al.  Are vertebrate exons scanned during splice-site selection? , 1992, Nature.

[93]  N. Proudfoot,et al.  Transcriptional termination between the closely linked human complement genes C2 and factor B: common termination factor for C2 and c‐myc? , 1991, The EMBO journal.

[94]  S. Berget,et al.  Mutation of the AAUAAA polyadenylation signal depresses in vitro splicing of proximal but not distal introns. , 1991, Genes & development.

[95]  J. Alwine,et al.  The human immunodeficiency virus type 1 polyadenylylation signal: a 3' long terminal repeat element upstream of the AAUAAA necessary for efficient polyadenylylation. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[96]  M. Imperiale,et al.  Involvement of long terminal repeat U3 sequences overlapping the transcription control region in human immunodeficiency virus type 1 mRNA 3' end formation , 1991, Molecular and cellular biology.

[97]  M. Wickens,et al.  Point mutations in AAUAAA and the poly (A) addition site: effects on the accuracy and efficiency of cleavage and polyadenylation in vitro. , 1990, Nucleic acids research.

[98]  J. Alwine,et al.  Efficiency of utilization of the simian virus 40 late polyadenylation site: effects of upstream sequences , 1989, Molecular and cellular biology.

[99]  N. Proudfoot,et al.  Definition of an efficient synthetic poly(A) site. , 1989, Genes & development.

[100]  N. Proudfoot How RNA polymerase II terminates transcription in higher eukaryotes. , 1989, Trends in biochemical sciences.

[101]  J. Butler,et al.  RNA processing generates the mature 3' end of yeast CYC1 messenger RNA in vitro. , 1988, Science.

[102]  C. Cole,et al.  Patterns of polyadenylation site selection in gene constructs containing multiple polyadenylation signals , 1988, Molecular and cellular biology.

[103]  D. Schümperli Multilevel regulation of replication-dependent histone genes. , 1988, Trends in genetics : TIG.

[104]  J. Manley,et al.  A functional mRNA polyadenylation signal is required for transcription termination by RNA polymerase II. , 1988, Genes & development.

[105]  J E Darnell,et al.  A poly(A) addition site and a downstream termination region are required for efficient cessation of transcription by RNA polymerase II in the mouse beta maj-globin gene. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[106]  N. Proudfoot,et al.  Position-dependent sequence elements downstream of AAUAAA are required for efficient rabbit β-globin mRNA 3′ end formation , 1987, Cell.

[107]  C. Cole,et al.  Fine-structure analysis of the processing and polyadenylation region of the herpes simplex virus type 1 thymidine kinase gene by using linker scanning, internal deletion, and insertion mutations , 1986, Molecular and cellular biology.

[108]  N. Proudfoot,et al.  Alpha‐thalassaemia caused by a poly(A) site mutation reveals that transcriptional termination is linked to 3′ end processing in the human alpha 2 globin gene. , 1986, The EMBO journal.

[109]  A. Krämer,et al.  Generation of histone mRNA 3′ ends by endonucleolytic cleavage of the pre‐mRNA in a snRNP‐dependent in vitro reaction. , 1986, The EMBO journal.

[110]  M. Birnstiel,et al.  Compensatory mutations suggest that base-pairing with a small nuclear RNA is required to form the 3′ end of H3 messenger RNA , 1986, Nature.

[111]  P. Sharp,et al.  Accurate cleavage and polyadenylation of exogenous RNA substrate , 1985, Cell.

[112]  J. McLauchlan,et al.  The consensus sequence YGTGTTYY located downstream from the AATAAA signal is required for efficient formation of mRNA 3' termini. , 1985, Nucleic acids research.

[113]  S. Orkin,et al.  Thalassemia due to a mutation in the cleavage‐polyadenylation signal of the human beta‐globin gene. , 1985, The EMBO journal.

[114]  M. Wickens,et al.  Role of the conserved AAUAAA sequence: four AAUAAA point mutants prevent messenger RNA 3' end formation. , 1984, Science.

[115]  N. Proudfoot,et al.  A sequence downstream of AAUAAA is required for rabbit β-globin mRNA 3′-end formation , 1984, Nature.

[116]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[117]  S. Goodbourn,et al.  α-Thalassaemia caused by a polyadenylation signal mutation , 1983, Nature.

[118]  Michael G. Rosenfeld,et al.  Alternative RNA processing in calcitonin gene expression generates mRNAs encoding different polypeptide products , 1982, Nature.

[119]  T. Shenk,et al.  The sequence 5′-AAUAAA-3′ forms part of the recognition site for polyadenylation of late SV40 mRNAs , 1981, Cell.

[120]  F. Sanger,et al.  DNA sequencing with chain-terminating inhibitors. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[121]  N. Proudfoot,et al.  The 3′ terminal sequences of human α and β globin messenger RNAs: Comparison with rabbit globin messenger RNA , 1976, Cell.

[122]  N. Proudfoot Sequence analysis of the 3′ non-coding regions of rabbit α- and β-globin messenger RNAs , 1976 .

[123]  N. Proudfoot,et al.  3′ Non-coding region sequences in eukaryotic messenger RNA , 1976, Nature.

[124]  T. Maniatis,et al.  Amplification and characterization of a β-globin gene synthesized in vitro , 1976, Cell.

[125]  A. Means,et al.  Preparation and preliminary characterization of purified ovalbumin messenger RNA from the hen oviduct. , 1975, Biochemistry.

[126]  F Galibert,et al.  Direct determination of DNA nucleotide sequences: structure of a fragment of bacteriophage phiX172 DNA. , 1974, Journal of molecular biology.

[127]  C. Milstein,et al.  Purification and sequence of messenger RNA for immunoglobulin light chains. , 1973, Nature: New biology.

[128]  H. Birnboim,et al.  Analysis of long pyrimidine polynucleotides in HeLa cell nuclear DNA: absence of polydeoxythymidylate. , 1973, Proceedings of the National Academy of Sciences of the United States of America.

[129]  M. Edmonds,et al.  A poly(A) polymerase from calf thymus. Purification and properities of the enzyme. , 1973, The Journal of biological chemistry.

[130]  M. Edmonds,et al.  A poly(A) polymerase from calf thymus. Characterization of the reaction product and the primer requirement. , 1973, The Journal of biological chemistry.

[131]  W. Jelinek,et al.  Further evidence on the nuclear origin and transfer to the cytoplasm of polyadenylic acid sequences in mammalian cell RNA. , 1973, Journal of molecular biology.

[132]  F. Sanger,et al.  Use of DNA polymerase I primed by a synthetic oligonucleotide to determine a nucleotide sequence in phage fl DNA. , 1973, Proceedings of the National Academy of Sciences of the United States of America.

[133]  J. Darnell,et al.  Evidence that all messenger RNA molecules (except histone messenger RNA) contain Poly (A) sequences and that the Poly(A) has a nuclear function. , 1972, Journal of molecular biology.

[134]  P. Leder,et al.  Purification of biologically active globin messenger RNA by chromatography on oligothymidylic acid-cellulose. , 1972, Proceedings of the National Academy of Sciences of the United States of America.

[135]  G. Brawerman,et al.  Characteristics of the polyadenylic acid segment associated with messenger ribonucleic acid in mouse sarcoma 180 ascites cells. , 1972, Biochemistry.

[136]  M. Mathews,et al.  Translation of globin messenger RNA in a heterologous cell-free system. , 1971, Nature.

[137]  H. Nakazato,et al.  Polyadenylic acid sequences in the heterogeneous nuclear RNA and rapidly-labeled polyribosomal RNA of HeLa cells: possible evidence for a precursor relationship. , 1971, Proceedings of the National Academy of Sciences of the United States of America.

[138]  E. Canellakis,et al.  Adenine-rich Polymer associated with Rabbit Reticulocyte Messenger RNA , 1970, Nature.

[139]  F. Sanger,et al.  Chromatography of 32P-labelled oligonucleotides on thin layers of DEAE-cellulose. , 1969, European journal of biochemistry.