Y RNA

Last updated
Y RNA
RF00019.jpg
Identifiers
SymbolY_RNA
Alt. SymbolsY1; Y3; Y4; Y5
Rfam RF00019
Other data
RNA type Gene
Domain(s) Eukaryota
SO SO:0000405
PDB structures PDBe

Y RNAs are small non-coding RNAs. They are components of the Ro60 ribonucleoprotein particle [1] which is a target of autoimmune antibodies in patients with systemic lupus erythematosus. [2] They are also reported to be necessary for DNA replication through interactions with chromatin and initiation proteins. [3] [4] However, mouse embryonic stem cells lacking Y RNAs are viable and have normal cell cycles. [5]

Contents

Structure

These small RNAs are predicted to fold into a conserved stem formed by the RNA's 3′ and 5′ ends and characterized by a single bulged cytosine, which are the known requirements for Ro binding. [6] [7] [8]

Function

Two functions have been described for Y RNAs in the literature: As a repressor of Ro60, and as an initiation factor for DNA replication. Mutant human Y RNAs lacking the conserved binding site for Ro60 protein still support DNA replication, [3] indicating that binding to Ro protein and promoting DNA replication are two separable functions of Y RNAs. Although Y RNA-derived small RNAs are similar in size to microRNAs, it has been shown that these Y RNA fragments are not involved in the microRNA pathway. [9]

The Ro autoantigen protein (white) binds the end of a double-stranded Y RNA (red) and a single stranded RNA (blue). (PDB: 1YVP ). YRNA-Ro60.png
The Ro autoantigen protein (white) binds the end of a double-stranded Y RNA (red) and a single stranded RNA (blue). ( PDB: 1YVP ).

Ro60 Inhibition

In its free state, Ro binds to a variety of misfolded RNAs including misfolded 5S rRNAs, and is thought to act as some sort of quality control mechanism. [10] Crystal structures of Ro complexed either with Y RNA or another RNA showed that Ro binds single-stranded 3′ ends of RNAs relatively nonspecifically, whereas Y RNA binds specifically at a second site that regulates access of other RNAs. [6] In Deinococcus , free Ro has also been shown to function in 23S rRNA maturation. [11] In Deinococcus, mutants lacking Y RNA are viable, and Y RNA appears to be unstable except when complexed with Ro. [11]

DNA replication initiation

Human Y RNAs are functionally required for DNA replication. [3] Biochemical fractionation and reconstitution experiments have established a functional requirement of human Y RNAs for chromosomal DNA replication in isolated vertebrate cell nuclei in vitro [3] and specific degradation of human Y RNAs inhibits DNA replication in vitro, and in intact cells in vivo . [3] Y RNA function is thought to be mediated via interactions with chromatin and initiation proteins (including the origin recognition complex) [4]

In human pathology

Y RNAs are overexpressed in some human tumours and are required for cell proliferation [12] and small, microRNA-sized breakdown products may be involved in autoimmunity and other pathological conditions. [13] Recent work has demonstrated that Y RNAs are modified at their 3′ end by the non-canonical poly(A) polymerase PAPD5, and the short oligo(A) tail added by PAPD5 is a marker for 3′ end processing by the ribonuclease PARN/EXOSC10 or for degradation by the exonuclease DIS3L. [14] Since PARN deficiency causes a severe form of the bone marrow disease Dyskeratosis Congenita as well as pulmonary fibrosis, [15] [16] it is possible that defects in Y RNA processing contribute to the severe pathology observed in these patients.

Species distribution

Presumptive Y RNA and Ro protein homologs have been found in eukaryotes and bacteria. [7] [17]

Humans

Humans appear to have four Y RNAs, named hY1, hY3, hY4 and hY5 [17] and also a large number of pseudogenes.

C. elegans

Caenorhabditis elegans has one, named CeY RNA and a large number of sbRNAs that are postulated to also be Y RNA homologues. [18] [19]

D. radiodurans

The radiation-resistant bacterium Deinococcus radiodurans encodes a homolog of Ro called rsr ("Ro sixty related"), and at least four small RNAs accumulate in Deinococcus under conditions where rsr expression is induced (UV irradiation); one of these RNAs appears to be a Y RNA homolog. [20] In Deinococcus radiodurans Rsr is tethered via Y RNA to the exoribonuclease PNPase and channels single-stranded RNA into the PNPase cavity. Rsr and Y RNA enhance degradation of structured RNAs by PNPase. This role could be conserved, as Rsr and ncRNAs called YrlA and YrlB (Y RNA like) also associate with PNPase in an evolutionary distant bacterium Salmonella Typhimurium. [21]

Related Research Articles

<span class="mw-page-title-main">Non-coding DNA</span> DNA not coding for protein

Non-coding DNA (ncDNA) sequences are components of an organism's DNA that do not encode protein sequences. Some non-coding DNA is transcribed into functional non-coding RNA molecules. Other functional regions of the non-coding DNA fraction include regulatory sequences that control gene expression; scaffold attachment regions; origins of DNA replication; centromeres; and telomeres. Some non-coding regions appear to be mostly nonfunctional such as introns, pseudogenes, intergenic DNA, and fragments of transposons and viruses.

<span class="mw-page-title-main">Non-coding RNA</span> Class of ribonucleic acid that is not translated into proteins

A non-coding RNA (ncRNA) is a functional RNA molecule that is not translated into a protein. The DNA sequence from which a functional non-coding RNA is transcribed is often called an RNA gene. Abundant and functionally important types of non-coding RNAs include transfer RNAs (tRNAs) and ribosomal RNAs (rRNAs), as well as small RNAs such as microRNAs, siRNAs, piRNAs, snoRNAs, snRNAs, exRNAs, scaRNAs and the long ncRNAs such as Xist and HOTAIR.

<span class="mw-page-title-main">Gene</span> Sequence of DNA or RNA that codes for an RNA or protein product

In biology, the word gene can have several different meanings. The Mendelian gene is a basic unit of heredity and the molecular gene is a sequence of nucleotides in DNA that is transcribed to produce a functional RNA. There are two types of molecular genes: protein-coding genes and noncoding genes.

<span class="mw-page-title-main">ILF3</span> Protein-coding gene in the species Homo sapiens

Interleukin enhancer-binding factor 3 is a protein that in humans is encoded by the ILF3 gene.

The perinucleolar compartment (PNC) is a subnuclear body characterized by its location at the periphery of the nucleolus. The PNC participates in the patterned compartmentalization inside the nucleus to organize the specialized functions. It is almost exclusively found in oncogenic cells and enriched with RNA binding proteins as well as RNA polymerase III transcripts.

<span class="mw-page-title-main">Sjögren syndrome antigen B</span>

Sjögren syndrome type B antigen (SS-B) also known as Lupus La protein is a protein that in humans is encoded by the SSB gene.

<span class="mw-page-title-main">TRIM21</span>

Tripartite motif-containing protein 21, also known as E3 ubiquitin-protein ligase TRIM21, is a protein that in humans is encoded by the TRIM21 gene. Alternatively spliced transcript variants for this gene have been described but the full-length nature of only one has been determined. It is expressed in most human tissues.

<span class="mw-page-title-main">CHAF1B</span> Protein-coding gene in the species Homo sapiens

Chromatin assembly factor 1 subunit B is a protein that in humans is encoded by the CHAF1B gene.

<span class="mw-page-title-main">ILF2</span> Protein-coding gene in the species Homo sapiens

Interleukin enhancer-binding factor 2 is a protein that in humans is encoded by the ILF2 gene.

<span class="mw-page-title-main">TROVE2</span> Protein-coding gene in the species Homo sapiens

60 kDa SS-A/Ro ribonucleoprotein is a protein that in humans is encoded by the TROVE2 gene.

<span class="mw-page-title-main">Exosome component 4</span> Protein-coding gene in the species Homo sapiens

Exosome component 4, also known as EXOSC4, is a human gene, which is part of the exosome complex.

<span class="mw-page-title-main">Exosome component 1</span> Protein-coding gene in the species Homo sapiens

3'-5' exoribonuclease CSL4 homolog is an enzyme that in humans is encoded by the EXOSC1 gene.

<span class="mw-page-title-main">REXO2</span>

REX2, RNA exonuclease 2 homolog , also known as REXO2, is an enzyme which in humans is encoded by the REXO2 gene.

<span class="mw-page-title-main">ZNF330</span> Protein-coding gene in the species Homo sapiens

Zinc finger protein 330 is a protein that in humans is encoded by the ZNF330 gene.

<span class="mw-page-title-main">Long non-coding RNA</span> Non-protein coding transcripts longer than 200 nucleotides

Long non-coding RNAs are a type of RNA, generally defined as transcripts more than 200 nucleotides that are not translated into protein. This arbitrary limit distinguishes long ncRNAs from small non-coding RNAs, such as microRNAs (miRNAs), small interfering RNAs (siRNAs), Piwi-interacting RNAs (piRNAs), small nucleolar RNAs (snoRNAs), and other short RNAs. Long intervening/intergenic noncoding RNAs (lincRNAs) are sequences of lncRNA which do not overlap protein-coding genes.

<span class="mw-page-title-main">HOTAIR</span> Gene found in humans

HOTAIR is a human gene located between HOXC11 and HOXC12 on chromosome 12. It is the first example of an RNA expressed on one chromosome that has been found to influence transcription of HOXD cluster posterior genes located on chromosome 2. The sequence and function of HOTAIR is different in human and mouse. Sequence analysis of HOTAIR revealed that it exists in mammals, has poorly conserved sequences and considerably conserved structures, and has evolved faster than nearby HoxC genes. A subsequent study identified HOTAIR has 32 nucleotide long conserved noncoding element (CNE) that has a paralogous copy in HOXD cluster region, suggesting that the HOTAIR conserved sequences predates whole genome duplication events at the root of vertebrate. While the conserved sequence paralogous with HOXD cluster is 32 nucleotide long, the HOTAIR sequence conserved from human to fish is about 200 nucleotide long and is marked by active enhancer features.

<i>Deinococcus radiodurans</i> Radioresistant extremophile species of bacterium

Deinococcus radiodurans is an extremophilic bacterium and one of the most radiation-resistant organisms known. It can survive cold, dehydration, vacuum, and acid, and therefore is known as a polyextremophile. It has been listed as the world's toughest known bacterium in The Guinness Book Of World Records.

sbRNA

sbRNA is a family of non-coding RNA first discovered in Caenorhabditis elegans. It was identified during a full transcriptome screen of the C. elegans cDNA library. Subsequent experimentation characterised sbRNA as having conserved 5' and 3' internal motifs which form a long paired stem which is interrupted with a bulge.

Deinococcus deserti is a Gram-negative, rod-shaped bacterium that belongs to the Deinococcaceae, a group of extremely radiotolerant bacteria. D. deserti and other Deinococcaceae exhibit an extraordinary ability to withstand ionizing radiation.

<span class="mw-page-title-main">Sandra Wolin</span> American microbiologist and physician-scientist

Sandra Lynn Wolin is an American microbiologist and physician-scientist specialized in biogenesis, function, and turnover of non-coding RNA. She is chief of the RNA Biology Laboratory at the National Cancer Institute.

References

  1. Hall AE, Turnbull C, Dalmay T (April 2013). "Y RNAs: recent developments". Biomolecular Concepts. 4 (2): 103–110. doi: 10.1515/bmc-2012-0050 . PMID   25436569. S2CID   12575326.
  2. Lerner MR, Boyle JA, Hardin JA, Steitz JA (January 1981). "Two novel classes of small ribonucleoproteins detected by antibodies associated with lupus erythematosus". Science. 211 (4480): 400–402. Bibcode:1981Sci...211..400L. doi:10.1126/science.6164096. PMID   6164096.
  3. 1 2 3 4 5 Christov CP, Gardiner TJ, Szüts D, Krude T (September 2006). "Functional requirement of noncoding Y RNAs for human chromosomal DNA replication". Molecular and Cellular Biology. 26 (18): 6993–7004. doi:10.1128/MCB.01060-06. PMC   1592862 . PMID   16943439.
  4. 1 2 Zhang AT, Langley AR, Christov CP, Kheir E, Shafee T, Gardiner TJ, Krude T (June 2011). "Dynamic interaction of Y RNAs with chromatin and initiation proteins during human DNA replication". Journal of Cell Science. 124 (Pt 12): 2058–2069. doi:10.1242/jcs.086561. PMC   3104036 . PMID   21610089.
  5. Leng Y, Sim S, Magidson V, Wolin SL (July 2020). "Noncoding Y RNAs regulate the levels,subcellular distribution and protein interactions of their Ro60 autoantigen partner". Nucleic Acids Research. 48 (12): 6919–6930. doi:10.1093/nar/gkaa414. PMC   7337961 . PMID   32469055.
  6. 1 2 3 Stein AJ, Fuchs G, Fu C, Wolin SL, Reinisch KM (May 2005). "Structural insights into RNA quality control: the Ro autoantigen binds misfolded RNAs via its central cavity". Cell. 121 (4): 529–539. doi:10.1016/j.cell.2005.03.009. PMC   1769319 . PMID   15907467.
  7. 1 2 Teunissen SW, Kruithof MJ, Farris AD, Harley JB, Venrooij WJ, Pruijn GJ (January 2000). "Conserved features of Y RNAs: a comparison of experimentally derived secondary structures". Nucleic Acids Research. 28 (2): 610–619. doi:10.1093/nar/28.2.610. PMC   102524 . PMID   10606662.
  8. Green CD, Long KS, Shi H, Wolin SL (July 1998). "Binding of the 60-kDa Ro autoantigen to Y RNAs: evidence for recognition in the major groove of a conserved helix". RNA. 4 (7): 750–765. doi:10.1017/S1355838298971667. PMC   1369656 . PMID   9671049.
  9. Nicolas FE, Hall AE, Csorba T, Turnbull C, Dalmay T (April 2012). "Biogenesis of Y RNA-derived small RNAs is independent of the microRNA pathway". FEBS Letters. 586 (8): 1226–1230. doi: 10.1016/j.febslet.2012.03.026 . PMID   22575660. S2CID   7805517.
  10. Reinisch KM, Wolin SL (April 2007). "Emerging themes in non-coding RNA quality control". Current Opinion in Structural Biology. 17 (2): 209–214. doi:10.1016/j.sbi.2007.03.012. PMID   17395456.
  11. 1 2 Chen X, Wurtmann EJ, Van Batavia J, Zybailov B, Washburn MP, Wolin SL (June 2007). "An ortholog of the Ro autoantigen functions in 23S rRNA maturation in D. radiodurans". Genes & Development. 21 (11): 1328–1339. doi:10.1101/gad.1548207. PMC   1877746 . PMID   17510283.
  12. Christov CP, Trivier E, Krude T (March 2008). "Noncoding human Y RNAs are overexpressed in tumours and required for cell proliferation". British Journal of Cancer. 98 (5): 981–988. doi:10.1038/sj.bjc.6604254. PMC   2266855 . PMID   18283318.
  13. Verhagen AP, Pruijn GJ (September 2011). "Are the Ro RNP-associated Y RNAs concealing microRNAs? Y RNA-derived miRNAs may be involved in autoimmunity". BioEssays. 33 (9): 674–682. doi:10.1002/bies.201100048. PMID   21735459. S2CID   26501077.
  14. Shukla S, Parker R (October 2017). "PARN Modulates Y RNA Stability and Its 3′-End Formation". Molecular and Cellular Biology. 37 (20). doi:10.1128/MCB.00264-17. PMC   5615183 . PMID   28760775.
  15. Stuart BD, Choi J, Zaidi S, Xing C, Holohan B, Chen R, Choi M, Dharwadkar P, Torres F, Girod CE, Weissler J, Fitzgerald J, Kershaw C, Klesney-Tait J, Mageto Y, Shay JW, Ji W, Bilguvar K, Mane S, Lifton RP, Garcia CK (May 2015). "Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening". Nature Genetics. 47 (5): 512–517. doi:10.1038/ng.3278. PMC   4414891 . PMID   25848748.
  16. Tummala H, Walne A, Collopy L, Cardoso S, de la Fuente J, Lawson S, Powell J, Cooper N, Foster A, Mohammed S, Plagnol V, Vulliamy T, Dokal I (May 2015). "Poly(A)-specific ribonuclease deficiency impacts telomere biology and causes dyskeratosis congenita". The Journal of Clinical Investigation. 125 (5): 2151–2160. doi:10.1172/JCI78963. PMC   4463202 . PMID   25893599.
  17. 1 2 Perreault J, Perreault JP, Boire G (August 2007). "Ro-associated Y RNAs in metazoans: evolution and diversification". Molecular Biology and Evolution. 24 (8): 1678–1689. doi: 10.1093/molbev/msm084 . PMID   17470436.
  18. Van Horn DJ, Eisenberg D, O'Brien CA, Wolin SL (May 1995). "Caenorhabditis elegans embryos contain only one major species of Ro RNP". RNA. 1 (3): 293–303. PMC   1369082 . PMID   7489501.
  19. Boria I, Gruber AR, Tanzer A, Bernhart SH, Lorenz R, Mueller MM, Hofacker IL, Stadler PF (April 2010). "Nematode sbRNAs: homologs of vertebrate Y RNAs". Journal of Molecular Evolution. 70 (4): 346–358. Bibcode:2010JMolE..70..346B. doi:10.1007/s00239-010-9332-4. PMID   20349053. S2CID   876486.
  20. Chen X, Quinn AM, Wolin SL (April 2000). "Ro ribonucleoproteins contribute to the resistance of Deinococcus radiodurans to ultraviolet irradiation". Genes & Development. 14 (7): 777–782. doi:10.1101/gad.14.7.777. PMC   316496 . PMID   10766734.
  21. Chen X, Taylor DW, Fowler CC, Galan JE, Wang HW, Wolin SL (March 2013). "An RNA degradation machine sculpted by Ro autoantigen and noncoding RNA". Cell. 153 (1): 166–177. doi:10.1016/j.cell.2013.02.037. PMC   3646564 . PMID   23540697.