Eukaryotic small ribosomal subunit (40S) explained

The eukaryotic small ribosomal subunit (40S) is the smaller subunit of the eukaryotic 80S ribosomes, with the other major component being the large ribosomal subunit (60S). The "40S" and "60S" names originate from the convention that ribosomal particles are denoted according to their sedimentation coefficients in Svedberg units. It is structurally and functionally related to the 30S subunit of 70S prokaryotic ribosomes.[1] [2] [3] [4] However, the 40S subunit is much larger than the prokaryotic 30S subunit and contains many additional protein segments, as well as rRNA expansion segments.

Function

The 40S subunit contains the decoding center which monitors the complementarity of tRNA and mRNA in protein translation. It is the largest component of several translation initiation complexes, including the 43S and 48S preinitiation complexes (PICs), being bound by several eukaryotic initiation factors, including eIF1, eIF1A, and eIF3.[5] The 40S ribosomal subunit is also tightly bound by the HCV IRES to form a binary complex mediate by protein-mRNA and rRNA-mRNA interactions.[6] More information can be found in the articles on the ribosome, the eukaryotic ribosome (80S), and the article on protein translation.

Overall structure

The shape of the small subunit can be subdivided into two large segments, the head and the body. Characteristic features of the body include the left and right feet, the shoulder and the platform. The head features a pointed protrusion reminiscent of a bird's beak. The mRNA binds in the cleft between the head and the body, and there are three binding sites for tRNA, the A-site, P-site and E-site (see article on protein translation for details).The core of the 40S subunit is formed by the 18S ribosomal RNA (abbreviated 18S rRNA), which is homologous to the prokaryotic 16S rRNA. This rRNA core is decorated with dozens of proteins. In the figure "Crystal Structure of the Eukaryotic 40S Ribosomal Subunit from T. thermophila", the ribosomal RNA core is represented as a grey tube and expansion segments are shown in red. Proteins which have homologs in eukaryotes, archaea and bacteria are shown as blue ribbons. Proteins shared only between eukaryotes and archaea are shown as orange ribbons and proteins specific to eukaryotes are shown as red ribbons.

40S ribosomal proteins

The table "40S ribosomal proteins" shows the individual protein folds of the 40S subunit colored by conservation. Proteins which have homologs in eukaryotes, archaea and bacteria (EAB) are shown as blue ribbons. Proteins shared only between eukaryotes and archaea (EA) are shown as orange ribbons and proteins specific to eukaryotes (E) are shown as red ribbons. Eukaryote-specific extensions of conserved proteins, ranging from a few residues or loops to very long alpha helices and additional domains, are highlighted in red.[1] For a details, refer to the article on the eukaryotic ribosome. Historically, different nomenclatures have been used for ribosomal proteins. For instance, proteins have been numbered according to their migration properties in gel electrophoresis experiments. Therefore, different names may refer to homologous proteins from different organism, while identical names not necessarily denote homologous proteins. The table "40S ribosomal proteins" crossreferences the human ribosomal protein names with yeast, bacterial and archaeal homologs. Further information can be found in the ribosomal protein gene database (RPG).

40S ribosomal proteins
Structure (Eukaryotic)[7] H. sapiens[8] [9] Universal name [10] Conservation[11] S. cerevisiae[12] Bacterial homolog (E. coli) Archaeal homolog
uS2 EABS0S2pS2
uS5 EABS2S5pS5p
uS3 EABS3S3pS3p
eS1 EAS1 n/aS3Ae
RPS4 (RPS4X, RPS4Y1, RPS4Y2) eS4 EAS4 n/aS4e
uS7 EABS5S7p S5p
eS6 EAS6n/aS6e
eS7 ES7 n/an/a
eS8 EAS8 n/a S8e
uS4 EABS9S4p S4p
eS10 ES10 n/a n/a
uS17 EABS11S17pS17p
eS12 ES12n/a n/a
uS15 EABS13S15pS15p
uS11 EABS14S11pS11p
uS19 EABS15S19pS19p
uS8 EABS22S8p S8p
uS9 EABS16S9p S9p
eS17 EAS17n/aS17e
uS13 EABS18S13pS13p
eS19 EAS19n/aS19e
uS10 EABS20S10pS10p
eS21 ES21n/an/a
uS12 EABS23S12pS12p
eS24 EAS24n/aS24e
eS25 EAS25n/aS25e
eS26 EAS26n/aS26e
eS27 EAS27n/aS27e
eS31 EAS31n/aS27ae
eS28 EAS28n/aS28e
uS14 EABS29S14pS14p
eS30 EAS30n/aS30e
RACK1 EAsc1n/an/a

See also

External links

Notes and References

  1. Rabl . J . Leibundgut . M . Ataide . SF . Haag . A . Ban . N . Feb 2011 . Crystal structure of the eukaryotic 40S ribosomal subunit in complex with initiation factor 1 . Science . 331 . 6018. 730–736 . 10.1126/science.1198308 . 21205638 . 2011Sci...331..730R . 20.500.11850/153130 . 24771575 . free .
  2. Ben-Shem . A . Garreau . de Loubresse . N . Melnikov . S . Jenner . L . Yusupova . G . Yusupov . M . Dec 2011 . The structure of the eukaryotic ribosome at 3.0 Å resolution . Science . 334 . 6062. 1524–1529 . 10.1126/science.1212642 . 22096102 . 2011Sci...334.1524B . 9099683 . free .
  3. Wimberly . BT . Brodersen . DE . Clemons . WM Jr . Morgan-Warren . RJ . Carter . AP . Vonrhein . C . Hartsch . T . Ramakrishnan . V . Sep 2000 . Structure of the 30S ribosomal subunit . Nature . 407 . 6802. 327–339 . 10.1038/35030006 . 11014182 . 2000Natur.407..327W . 4419944 .
  4. Schmeing . TM . Ramakrishnan . V . Oct 2009 . What recent ribosome structures have revealed about the mechanism of translation . Nature . 461 . 7268. 1234–1242 . 10.1038/nature08403 . 19838167 . 2009Natur.461.1234S . 4398636 .
  5. Aitken. Colin E.. Lorsch. Jon R.. A mechanistic overview of translation initiation in eukaryotes. Nat. Struct. Mol. Biol.. 2012. 19. 6. 568–576. 10.1038/nsmb.2303. 22664984. 9201095.
  6. Lytle JR, Wu L, Robertson HD . Domains on the hepatitis C virus internal ribosome entry site for 40s subunit binding . RNA . 8 . 8 . 1045–1055 . August 2002 . 12212848 . 10.1017/S1355838202029965. 1370315.
  7. Structure of the 'T. thermophila,' proteins from the structures of the large subunit PDBS 417, 4A19 and small subunit PDB 2XZM
  8. Nakao . A . Yoshihama . M . Kenmochi . N . 2004 . RPG: the Ribosomal Protein Gene database . Nucleic Acids Res. . 32 . Database issue. D168–70 . 10.1093/nar/gkh004 . 14681386 . 308739.
  9. Nomenclature according to the ribosomal protein gene database, applies to H. sapiens and T. thermophila
  10. Ban . Nenad . Beckmann . Roland . Cate . Jamie HD . Dinman . Jonathan D . Dragon . François . Ellis . Steven R . Lafontaine . Denis LJ . Lindahl . Lasse . Liljas . Anders . Lipton . Jeffrey M . McAlear . Michael A . Moore . Peter B . Noller . Harry F . Ortega . Joaquin . Panse . Vikram Govind . Ramakrishnan . V . Spahn . Christian MT . Steitz . Thomas A . Tchorzewski . Marek . Tollervey . David . Warren . Alan J . Williamson . James R . Wilson . Daniel . Yonath . Ada . Yusupov . Marat . A new system for naming ribosomal proteins . Current Opinion in Structural Biology . Elsevier BV . 24 . 2014 . 0959-440X . 10.1016/j.sbi.2014.01.002 . 165–169. 11603/14279 . free . 24524803 . 4358319 .
  11. EAB means conserved in eukaryotes, archaea and bacteria, EA means conserved in eukaryotes and archaea and E means eukaryote-specific protein
  12. Traditionally, ribosomal proteins were named according to their apparent molecular weight in gel electrophoresis, leading to different names for homologous proteins from different organisms. The RPG offers a unified nomenclature for ribosomal protein genes based on homology.