PSMC3 explained

26S protease regulatory subunit 6A, also known as 26S proteasome AAA-ATPase subunit Rpt5, is an enzyme that in humans is encoded by the PSMC3 gene.[1] [2] This protein is one of the 19 essential subunits of a complete assembled 19S proteasome complex[3] Six 26S proteasome AAA-ATPase subunits (Rpt1, Rpt2, Rpt3, Rpt4, Rpt5 (this protein), and Rpt6) together with four non-ATPase subunits (Rpn1, Rpn2, Rpn10, and Rpn13) form the base sub complex of 19S regulatory particle for proteasome complex.[3]

Gene

The gene PSMC3 encodes one of the ATPase subunits, a member of the triple-A family of ATPases that have chaperone-like activity. This subunit may compete with PSMC2 for binding to the HIV tat protein to regulate the interaction between the viral protein and the transcription complex. A pseudogene has been identified on chromosome 9.[4] The human PSMC3 gene has 12 exons and locates at chromosome band 11p11.2.

Protein

The human protein 26S protease regulatory subunit 6A is 49kDa in size and composed of 439 amino acids. The calculated theoretical pI of this protein is 5.68.[5]

Complex assembly

26S proteasome complex is usually consisted of a 20S core particle (CP, or 20S proteasome) and one or two 19S regulatory particles (RP, or 19S proteasome) on either one side or both side of the barrel-shaped 20S. The CP and RPs pertain distinct structural characteristics and biological functions. In brief, 20S sub complex presents three types proteolytic activities, including caspase-like, trypsin-like, and chymotrypsin-like activities. These proteolytic active sites located in the inner side of a chamber formed by 4 stacked rings of 20S subunits, preventing random protein-enzyme encounter and uncontrolled protein degradation. The 19S regulatory particles can recognize ubiquitin-labeled protein as degradation substrate, unfold the protein to linear, open the gate of 20S core particle, and guide the substrate into the proteolytic chamber. To meet such functional complexity, 19S regulatory particle contains at least 18 constitutive subunits. These subunits can be categorized into two classes based on the ATP dependence of subunits, ATP-dependent subunits and ATP-independent subunits. According to the protein interaction and topological characteristics of this multisubunit complex, the 19S regulatory particle is composed of a base and a lid subcomplex. The base consists of a ring of six AAA ATPases (Subunit Rpt1-6, systematic nomenclature) and four non-ATPase subunits (Rpn1, Rpn2, Rpn10, and Rpn13). Thus, 26S protease regulatory subunit 4 (Rpt2) is an essential component of forming the base subcomplex of 19S regulatory particle. For the assembly of 19S base sub complex, four sets of pivotal assembly chaperons (Hsm3/S5b, Nas2/P27, Nas6/P28, and Rpn14/PAAF1, nomenclature in yeast/mammals) were identified by four groups independently.[6] [7] [8] [9] [10] [11] These 19S regulatory particle base-dedicated chaperons all binds to individual ATPase subunits through the C-terminal regions. For example, Hsm3/S5b binds to the subunit Rpt1 and Rpt2 (this protein), Nas2/p27 to Rpt5 (this protein), Nas6/p28 to Rpt3, and Rpn14/PAAAF1 to Rpt6, respectively. Subsequently, three intermediate assembly modules are formed as following, the Nas6/p28-Rpt3-Rpt6-Rpn14/PAAF1 module, the Nas2/p27-Rpt4-Rpt5 module, and the Hsm3/S5b-Rpt1-Rpt2-Rpn2 module. Eventually, these three modules assemble together to form the heterohexameric ring of 6 Atlases with Rpn1. The final addition of Rpn13 indicates the completion of 19S base sub complex assembly.[3]

Function

As the degradation machinery that is responsible for ~70% of intracellular proteolysis,[12] proteasome complex (26S proteasome) plays a critical roles in maintaining the homeostasis of cellular proteome. Accordingly, misfolded proteins and damaged protein need to be continuously removed to recycle amino acids for new synthesis; in parallel, some key regulatory proteins fulfill their biological functions via selective degradation; furthermore, proteins are digested into peptides for MHC class I antigen presentation. To meet such complicated demands in biological process via spatial and temporal proteolysis, protein substrates have to be recognized, recruited, and eventually hydrolyzed in a well controlled fashion. Thus, 19S regulatory particle pertains a series of important capabilities to address these functional challenges. To recognize protein as designated substrate, 19S complex has subunits that are capable to recognize proteins with a special degradative tag, the ubiquitinylation. It also have subunits that can bind with nucleotides (e.g., ATPs) in order to facilitate the association between 19S and 20S particles, as well as to cause confirmation changes of alpha subunit C-terminals that form the substrate entrance of 20S complex.

The ATPases subunits assemble into a six-membered ring with a sequence of Rpt1–Rpt5–Rpt4–Rpt3–Rpt6–Rpt2, which interacts with the seven-membered alpha ring of 20S core particle and establishes an asymmetric interface between the 19S RP and the 20S CP.[13] [14] Three C-terminal tails with HbYX motifs of distinct Rpt ATPases insert into pockets between two defined alpha subunits of the CP and regulate the gate opening of the central channels in the CP alpha ring.[15] [16] Evidence showed that ATPase subunit Rpt5, along with other ubuiqintinated 19S proteasome subunits (Rpn13, Rpn10) and the deubiquitinating enzyme Uch37, can be ubiquitinated in situ by proteasome-associating ubiquitination enzymes. Ubiquitination of proteasome subunits can regulates proteasomal activity in response to the alteration of cellular ubiquitination levels.[17]

Interactions

PSMC3 has been shown to interact with PSMC5[18] and Von Hippel-Lindau tumor suppressor.[19]

Further reading

Notes and References

  1. Hoyle J, Tan KH, Fisher EM . Localization of genes encoding two human one-domain members of the AAA family: PSMC5 (the thyroid hormone receptor-interacting protein, TRIP1) and PSMC3 (the Tat-binding protein, TBP1) . Hum Genet . 99 . 2 . 285–8 . Mar 1997 . 9048938 . 10.1007/s004390050356 . 29818936 .
  2. Tanahashi N, Suzuki M, Fujiwara T, Takahashi E, Shimbara N, Chung CH, Tanaka K . Chromosomal localization and immunological analysis of a family of human 26S proteasomal ATPases . Biochem Biophys Res Commun . 243 . 1 . 229–32 . Mar 1998 . 9473509 . 10.1006/bbrc.1997.7892 .
  3. Gu ZC, Enenkel C . Proteasome assembly . Cellular and Molecular Life Sciences . 71 . 24 . 4729–45 . Dec 2014 . 25107634 . 10.1007/s00018-014-1699-8 . 15661805 . 11113775 .
  4. Web site: Entrez Gene: PSMC3 proteasome (prosome, macropain) 26S subunit, ATPase, 3.
  5. Web site: Uniprot: P17980 - PRS6A_HUMAN.
  6. Le Tallec B, Barrault MB, Guérois R, Carré T, Peyroche A . Hsm3/S5b participates in the assembly pathway of the 19S regulatory particle of the proteasome . Molecular Cell . 33 . 3 . 389–99 . Feb 2009 . 19217412 . 10.1016/j.molcel.2009.01.010 . free .
  7. Funakoshi M, Tomko RJ, Kobayashi H, Hochstrasser M . Multiple assembly chaperones govern biogenesis of the proteasome regulatory particle base . Cell . 137 . 5 . 887–99 . May 2009 . 19446322 . 2718848 . 10.1016/j.cell.2009.04.061 .
  8. Park S, Roelofs J, Kim W, Robert J, Schmidt M, Gygi SP, Finley D . Hexameric assembly of the proteasomal ATPases is templated through their C termini . Nature . 459 . 7248 . 866–70 . Jun 2009 . 19412160 . 2722381 . 10.1038/nature08065 . 2009Natur.459..866P .
  9. Roelofs J, Park S, Haas W, Tian G, McAllister FE, Huo Y, Lee BH, Zhang F, Shi Y, Gygi SP, Finley D . Chaperone-mediated pathway of proteasome regulatory particle assembly . Nature . 459 . 7248 . 861–5 . Jun 2009 . 19412159 . 2727592 . 10.1038/nature08063 . 2009Natur.459..861R .
  10. Saeki Y, Toh-E A, Kudo T, Kawamura H, Tanaka K . Multiple proteasome-interacting proteins assist the assembly of the yeast 19S regulatory particle . Cell . 137 . 5 . 900–13 . May 2009 . 19446323 . 10.1016/j.cell.2009.05.005 . 14151131 . free .
  11. Kaneko T, Hamazaki J, Iemura S, Sasaki K, Furuyama K, Natsume T, Tanaka K, Murata S . Assembly pathway of the Mammalian proteasome base subcomplex is mediated by multiple specific chaperones . Cell . 137 . 5 . 914–25 . May 2009 . 19490896 . 10.1016/j.cell.2009.05.008 . 18551885 . free .
  12. Rock KL, Gramm C, Rothstein L, Clark K, Stein R, Dick L, Hwang D, Goldberg AL . Inhibitors of the proteasome block the degradation of most cell proteins and the generation of peptides presented on MHC class I molecules . Cell . 78 . 5 . 761–71 . Sep 1994 . 8087844 . 10.1016/s0092-8674(94)90462-6. 22262916 .
  13. Tian G, Park S, Lee MJ, Huck B, McAllister F, Hill CP, Gygi SP, Finley D . An asymmetric interface between the regulatory and core particles of the proteasome . Nature Structural & Molecular Biology . 18 . 11 . 1259–67 . Nov 2011 . 22037170 . 3210322 . 10.1038/nsmb.2147 .
  14. Lander GC, Estrin E, Matyskiela ME, Bashore C, Nogales E, Martin A . Complete subunit architecture of the proteasome regulatory particle . Nature . 482 . 7384 . 186–91 . Feb 2012 . 22237024 . 3285539 . 10.1038/nature10774 . 2012Natur.482..186L .
  15. Gillette TG, Kumar B, Thompson D, Slaughter CA, DeMartino GN . Differential roles of the COOH termini of AAA subunits of PA700 (19 S regulator) in asymmetric assembly and activation of the 26 S proteasome . The Journal of Biological Chemistry . 283 . 46 . 31813–31822 . Nov 2008 . 18796432 . 2581596 . 10.1074/jbc.M805935200 . free .
  16. Smith DM, Chang SC, Park S, Finley D, Cheng Y, Goldberg AL . Docking of the proteasomal ATPases' carboxyl termini in the 20S proteasome's alpha ring opens the gate for substrate entry . Molecular Cell . 27 . 5 . 731–744 . Sep 2007 . 17803938 . 2083707 . 10.1016/j.molcel.2007.06.033 .
  17. Jacobson AD, MacFadden A, Wu Z, Peng J, Liu CW . Autoregulation of the 26S proteasome by in situ ubiquitination . Molecular Biology of the Cell . 25 . 12 . 1824–35 . Jun 2014 . 24743594 . 4055262 . 10.1091/mbc.E13-10-0585 .
  18. Ishizuka T, Satoh T, Monden T, Shibusawa N, Hashida T, Yamada M, Mori M . Human immunodeficiency virus type 1 Tat binding protein-1 is a transcriptional coactivator specific for TR . Mol. Endocrinol. . 15 . 8 . 1329–43 . Aug 2001 . 11463857 . 10.1210/mend.15.8.0680 . free .
  19. Corn PG, McDonald ER, Herman JG, El-Deiry WS . Tat-binding protein-1, a component of the 26S proteasome, contributes to the E3 ubiquitin ligase function of the von Hippel-Lindau protein . Nat. Genet. . 35 . 3 . 229–37 . Nov 2003 . 14556007 . 10.1038/ng1254 . 22798700 .

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