MALT1

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MALT1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesMALT1, IMD12, MLT, MLT1, PCASP1, MALT1 paracaspase
External IDsOMIM: 604860 MGI: 2445027 HomoloGene: 4938 GeneCards: MALT1
Orthologs
SpeciesHumanMouse
Entrez

10892

240354

Ensembl

ENSG00000172175

ENSMUSG00000032688

UniProt

Q9UDY8

Q2TBA3

RefSeq (mRNA)

NM_006785
NM_173844

NM_172833
NM_001365019

RefSeq (protein)

NP_006776
NP_776216

NP_766421
NP_001351948

Location (UCSC)Chr 18: 58.67 – 58.75 MbChr 18: 65.56 – 65.61 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Mucosa-associated lymphoid tissue lymphoma translocation protein 1 is a protein that in humans is encoded by the MALT1 gene.[5][6][7] It's the human paracaspase.

Function

Genetic ablation of the paracaspase gene in mice and biochemical studies have shown that paracaspase is a crucial protein for T and B lymphocytes activation. It has an important role in the activation of the transcription factor NF-κB, in the production of interleukin-2 (IL-2) and in T and B lymphocytes proliferation[8][9] Two alternatively spliced transcript variants encoding different isoforms have been described for this gene.[10]

In addition, a role for paracaspase has been shown in the innate immune response mediated by the zymosan receptor Dectin-1 in macrophages and dendritic cells, and in response to the stimulation of certain G protein-coupled receptors.[11]

Sequence analysis proposes that paracaspase has an N-terminal death domain, two central immunoglobulin-like domains involved in the binding to the B-cell lymphoma 10 (Bcl10) protein and a caspase-like domain. The death domain and immunoglobulin-like domains participate in binding to BCL10. Activation of MALT1 downstream NF-κB signaling and protease activity occurs when BCL10/MALT1 gets recruited to an activated CARD-CC family protein (CARD9, -10, -11 or -14) in a so-called CBM (CARD-CC/BCL10/MALT1) signaling complex.

Paracaspase has been shown to have proteolytic activity through its caspase-like domain in T lymphocytes. Cysteine 464 and histidine 414 are crucial for this activity. Like metacaspases, the paracaspase cleaves substrates after an arginine residue. To date, several paracaspase substrates have been described (see below). Bcl10 is cut after arginine 228. This removes the last five amino acids at the C-terminus and is crucial for T cell adhesion to fibronectin, but not for NF-κB activation and IL-2 production. However, using a peptide-based inhibitor (z-VRPR-fmk) of the paracaspase proteolytic activity, it has been shown that this activity is required for a sustain NF-κB activation and IL-2 production, suggesting that paracaspase may have others substrates involved in T cell-mediated NF-κB activation.[12] A20, a deubiquitinase, has been shown to be cut by paracaspase in Human and in mouse. Cells expressing an uncleavable A20 mutant is however still capable to activate NF-κB, but cells expressing the C-terminal or the N-terminal A20 cleavage products activates more NF-κB than cells expressing wild-type A20, indicating that cleavage of A20 leads to its inactivation. Since A20 has been described has an inhibitor of NF-κB, this suggests that paracaspase-mediated A20 cleavage in T lymphocytes is necessary for a proper NF-κB activation.[13]

By targeting paracaspase proteolytic activity, it might be possible to develop new drugs that might be useful for the treatment of certain lymphomas or autoimmune disorders.

Interactions

MALT1 has been shown to interact with BCL10,[14] TRAF6 and SQSTM1/p62.

Protease substrates

MALT1 (PCASP1) is part of the paracaspase family and shows proteolytic activity. Since many of the substrates are involved in regulation of inflammatory responses, the protease activity of MALT1 has emerged as an interesting therapeutic target. Currently known protease substrates are (in order of reported discovery):

MALT1 protease substrates
Substrate Reference Cleavage sequence
A20 (TNFAIP3) [13] LGASR/G
BCL10 [12] LRSR/T
CYLD [15] FMSR/G
RELB [16] LVSR/G
regnase-1/MCPIP1 (ZC3H12A) [17] LVPR/G
Roquin-1 (RC3H1) [18] LIPR/G
Roquin-2 (RC3H2) [18] LISR/S
MALT1 auto-proteolysis [19] LCCR/A
MALT1 auto-proteolysis [20] HCSR/T
HOIL1 (RBCK1) [21][22][23] LQPR/G
N4BP1 [24] FVSR/G
CARD10 [25] LRCR/G
ZC3H12D [26] LVPR/G
ZC3H12B [26] LVPR/G
TAB3 [26] LQSR/G
CASP10 [26] LVSR/G
CILK1 [26] LISR/S
ILDR2 [26] GASR/G LVSR/T GASR/G
TANK [26] HIPR/V
Tensin-3 [27] R614, R645


Specifically by the oncogenic IAP2-MALT1 fusion:

Protease inhibitors

Since MALT1 protease activity is a promising therapeutic target, several different screenings have been performed which have resulted in different types of protease inhibitors.[30] There is active competition between multiple pharma companies and independent research groups in drug development against the MALT1 protease activity.[31]

See also

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000172175 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000032688 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Dierlamm J, Baens M, Wlodarska I, Stefanova-Ouzounova M, Hernandez JM, Hossfeld DK, et al. (June 1999). "The apoptosis inhibitor gene API2 and a novel 18q gene, MLT, are recurrently rearranged in the t(11;18)(q21;q21) associated with mucosa-associated lymphoid tissue lymphomas". Blood. 93 (11): 3601–9. doi:10.1182/blood.V93.11.3601. PMID 10339464.
  6. ^ Hosaka S, Akamatsu T, Nakamura S, Kaneko T, Kitano K, Kiyosawa K, et al. (July 1999). "Mucosa-associated lymphoid tissue (MALT) lymphoma of the rectum with chromosomal translocation of the t(11;18)(q21;q21) and an additional aberration of trisomy 3". Am J Gastroenterol. 94 (7): 1951–4. doi:10.1111/j.1572-0241.1999.01237.x. PMID 10406266. S2CID 188457.
  7. ^ Akagi T, Motegi M, Tamura A, Suzuki R, Hosokawa Y, Suzuki H, et al. (November 1999). "A novel gene, MALT1 at 18q21, is involved in t(11;18) (q21;q21) found in low-grade B-cell lymphoma of mucosa-associated lymphoid tissue". Oncogene. 18 (42): 5785–94. doi:10.1038/sj.onc.1203018. PMID 10523859.
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  18. ^ a b Jeltsch KM, Hu D, Brenner S, Zöller J, Heinz GA, Nagel D, et al. (2014). "Cleavage of roquin and regnase-1 by the paracaspase MALT1 releases their cooperatively repressed targets to promote T(H)17 differentiation". Nat Immunol. 15 (11): 1079–89. doi:10.1038/ni.3008. PMID 25282160. S2CID 8140814.
  19. ^ Baens M, Bonsignore L, Somers R, Vanderheydt C, Weeks SD, Gunnarsson J, Nilsson E, Roth RG, Thome M, Marynen P (2014). "MALT1 auto-proteolysis is essential for NF-κB-dependent gene transcription in activated lymphocytes". PLOS ONE. 9 (8): e103774. Bibcode:2014PLoSO...9j3774B. doi:10.1371/journal.pone.0103774. PMC 4126661. PMID 25105596.
  20. ^ Ginster S, Bardet M, Unterreiner A, Malinverni C, Renner F, Lam S, et al. (2017). "Two Antagonistic MALT1 Auto-Cleavage Mechanisms Reveal a Role for TRAF6 to Unleash MALT1 Activation". PLOS ONE. 12 (1): e0169026. Bibcode:2017PLoSO..1269026G. doi:10.1371/journal.pone.0169026. PMC 5214165. PMID 28052131.
  21. ^ Klein T, Fung SY, Renner F, Blank MA, Dufour A, Kang S, Bolger-Munro M, Scurll JM, Priatel JJ, Schweigler P, Melkko S, Gold MR, Viner RI, Régnier CH, Turvey SE, Overall CM (2015). "The paracaspase MALT1 cleaves HOIL1 reducing linear ubiquitination by LUBAC to dampen lymphocyte NF-κB signalling". Nat. Commun. 6: 8777. Bibcode:2015NatCo...6.8777K. doi:10.1038/ncomms9777. PMC 4659944. PMID 26525107.
  22. ^ Elton L, Carpentier I, Staal J, Driege Y, Haegman M, Beyaert R (2015). "MALT1 cleaves the E3 ubiquitin ligase HOIL-1 in activated T cells, generating a dominant negative inhibitor of LUBAC-induced NF-κB signaling". FEBS J. 283 (3): 403–12. doi:10.1111/febs.13597. PMID 26573773.
  23. ^ Douanne T, Gavard J, Bidère N (May 2016). "The paracaspase MALT1 cleaves the LUBAC subunit HOIL1 during antigen receptor signaling" (PDF). Journal of Cell Science. 129 (9): 1775–80. doi:10.1242/jcs.185025. PMID 27006117. S2CID 31415485.
  24. ^ Yamasoba D, Sato K, Ichinose T, Imamura T, Koepke L, Joas S, et al. (May 2019). "N4BP1 restricts HIV-1 and its inactivation by MALT1 promotes viral reactivation". Nature Microbiology. 4 (9): 1532–1544. doi:10.1038/s41564-019-0460-3. hdl:2433/244207. PMID 31133753. S2CID 167207661.
  25. ^ Israël L, Glück A, Berger M, Coral M, Ceci M, Unterreiner A, et al. (2021). "CARD10 cleavage by MALT1 restricts lung carcinoma growth in vivo". Oncogenesis. 10 (4): 32. doi:10.1038/s41389-021-00321-2. PMC 8024357. PMID 33824280.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  26. ^ a b c d e f g Bell PA, Scheuermann S, Renner F, Pan CL, Lu HY, Turvey SE, Bornancin F, Régnier CH, Overall CM (2022-08-19). "Integrating knowledge of protein sequence with protein function for the prediction and validation of new MALT1 substrates". Computational and Structural Biotechnology Journal. 20: 4717–4732. doi:10.1016/j.csbj.2022.08.021. ISSN 2001-0370. PMC 9463181. PMID 36147669.
  27. ^ Juilland M, Alouche N, Ubezzi I, Gonzalez M, Rashid HO, Scarpellino L, Erdmann T, Grau M, Lenz G, Luther SA, Thome M (2023-12-26). "Identification of Tensin-3 as a MALT1 substrate that controls B cell adhesion and lymphoma dissemination". Proceedings of the National Academy of Sciences. 120 (52): –2301155120. Bibcode:2023PNAS..12001155J. doi:10.1073/pnas.2301155120. PMC 10756297. PMID 38109544.
  28. ^ Rosebeck S, Madden L, Jin X, Gu S, Apel IJ, Appert A, Hamoudi RA, Noels H, Sagaert X, Van Loo P, Baens M, Du MQ, Lucas PC, McAllister-Lucas LM (2011). "Cleavage of NIK by the API2-MALT1 fusion oncoprotein leads to noncanonical NF-kappaB activation". Science. 331 (6016): 468–72. Bibcode:2011Sci...331..468R. doi:10.1126/science.1198946. PMC 3124150. PMID 21273489.
  29. ^ Nie Z, Du MQ, McAllister-Lucas LM, Lucas PC, Bailey NG, Hogaboam CM, Lim MS, Elenitoba-Johnson KS (2015). "Conversion of the LIMA1 tumour suppressor into an oncogenic LMO-like protein by API2-MALT1 in MALT lymphoma". Nat. Commun. 6 (5908): 5908. Bibcode:2015NatCo...6.5908N. doi:10.1038/ncomms6908. PMID 25569716.
  30. ^ Demeyer A, Staal J, Beyaert R (February 2016). "Targeting MALT1 Proteolytic Activity in Immunity, Inflammation and Disease: Good or Bad?". Trends in Molecular Medicine. 22 (2): 135–150. doi:10.1016/j.molmed.2015.12.004. PMID 26787500.
  31. ^ Hamp I, O'Neill TJ, Plettenburg O, Krappmann D (2021). "A patent review of MALT1 inhibitors (2013-present)". Expert Opin Ther Pat. 31 (12): 1079–1096. doi:10.1080/13543776.2021.1951703. PMID 34214002. S2CID 235723498.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  32. ^ Clinical trial number NCT03900598 for "A Study of JNJ-67856633 in Participants With Non-Hodgkin's Lymphoma (NHL) and Chronic Lymphocytic Leukemia (CLL)" at ClinicalTrials.gov
  33. ^ Nagel D, Spranger S, Vincendeau M, Grau M, Raffegerst S, Kloo B, et al. (December 2012). "Pharmacologic inhibition of MALT1 protease by phenothiazines as a therapeutic approach for the treatment of aggressive ABC-DLBCL". Cancer Cell. 22 (6): 825–37. doi:10.1016/j.ccr.2012.11.002. PMID 23238017.
  34. ^ Jacobs KA, André-Grégoire G, Maghe C, Li Y, Thys A, Harford-Wright E, et al. (2019-01-01). "Control of the Endo-Lysosome Homeostasis by the Paracaspase MALT1 regulates Glioma Cell Survival". bioRxiv: 582221. doi:10.1101/582221.
  35. ^ Konczalla L, Perez DR, Wenzel N, Wolters-Eisfeld G, Klemp C, Lüddeke J, Wolski A, Landschulze D, Meier C, Buchholz A, Yao D, Hofmann BT, Graß JK, Spriestersbach SL, Grupp K, Schumacher U, Betzel C, Kapis S, Nuguid T, Steinberg P, Püschel K, Sauter G, Bockhorn M, Uzunoglu FG, Izbicki JR, Güngör C, El Gammal AT (2019-07-10). "Biperiden and Mepazine effectively inhibit MALT1 activity and tumor growth in pancreatic cancer". International Journal of Cancer. 146 (6): 1618–1630. doi:10.1002/ijc.32567. ISSN 1097-0215. PMID 31291468.
  36. ^ Fontan L, Yang C, Kabaleeswaran V, Volpon L, Osborne MJ, Beltran E, et al. (December 2012). "MALT1 small molecule inhibitors specifically suppress ABC-DLBCL in vitro and in vivo". Cancer Cell. 22 (6): 812–24. doi:10.1016/j.ccr.2012.11.003. PMC 3984478. PMID 23238016.
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  41. ^ Quancard J, Klein T, Fung SY, Renatus M, Hughes N, Israël L, et al. (March 2019). "An allosteric MALT1 inhibitor is a molecular corrector rescuing function in an immunodeficient patient". Nature Chemical Biology. 15 (3): 304–313. doi:10.1038/s41589-018-0222-1. PMID 30692685. S2CID 59340695.
  42. ^ a b Cain C (2014-02-06). "Germinating MALT1". SciBX: Science-Business EXchange. 7 (5): 133. doi:10.1038/scibx.2014.133.
  43. ^ "VIB, CD3 and Galapagos NV enter license deal for the development of MALT1 inhibitors". Science|Business. Retrieved 2019-05-31.
  44. ^ Schiesser S, Hajek P, Pople HE, Käck H, Öster L, Cox RJ (October 2021). "Discovery and optimization of cyclohexane-1,4-diamines as allosteric MALT1 inhibitors" (PDF). European Journal of Medicinal Chemistry. 227: 113925. doi:10.1016/j.ejmech.2021.113925. PMID 34742013. S2CID 239486242.
  45. ^ "India's first-in-class MALT1 blocker deal". Nature Biotechnology. 37 (2): 112. 2019-02-04. doi:10.1038/s41587-019-0026-1. PMID 30718871. S2CID 59603303.
  46. ^ "Chordia Therapeutics Raises Approximately 27 million USD in Series B Financing" (PDF). 2019-03-29. Retrieved 2019-05-31.
  47. ^ "Hit to development candidate in 10 months: Rapid discovery of a novel, potent MALT1 inhibitor". 2024-03-20. Retrieved 2024-03-20.
  48. ^ "Schrödinger Highlights Discovery of SGR-1505, Clinical-Stage MALT1 Inhibitor, at American Chemical Society National Meeting" (Press release). 2024-03-20. Retrieved 2024-03-20.

Further reading

  • Bertoni F, Cavalli F, Cotter FE, Zucca E (2003). "Genetic alterations underlying the pathogenesis of MALT lymphoma". Hematol. J. 3 (1): 10–3. doi:10.1038/sj.thj.6200146. PMID 11960389.

External links

  • Overview of all the structural information available in the PDB for UniProt: Q9UDY8 (Mucosa-associated lymphoid tissue lymphoma translocation protein 1) at the PDBe-KB.
Retrieved from "https://mdwiki.org/wiki/MALT1"