TASP1

Threonine aspartase 1 is an enzyme that in humans is encoded by the TASP1 gene.[5][6]

TASP1
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 2A8I, 2A8J, 2A8L, 2A8M
Identifiers
Aliases	TASP1, C20orf13, dJ585I14.2, taspase 1
External IDs	OMIM: 608270 MGI: 1923062 HomoloGene: 9795 GeneCards: TASP1
Gene location (Human) Chr. Chromosome 20 (human)[1] Band 20p12.1 Start 13,389,392 bp[1] End 13,638,932 bp[1]
Gene location (Mouse) Chr. Chromosome 2 (mouse)[2] Band 2|2 F3 Start 139,833,480 bp[2] End 140,066,805 bp[2]
RNA expression pattern More reference expression data
Gene ontology Molecular function • peptidase activity • hydrolase activity • threonine-type endopeptidase activity • identical protein binding Cellular component • cytoplasm Biological process • positive regulation of transcription, DNA-templated • proteolysis • protein maturation Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	55617	75812
Ensembl	ENSG00000089123	ENSMUSG00000039033
UniProt	Q9H6P5	Q8R1G1
RefSeq (mRNA)	NM_017714 NM_001323602 NM_001323603 NM_001323604	NM_001159640 NM_001159641 NM_001289611 NM_175225
RefSeq (protein)	NP_001310531 NP_001310532 NP_001310533 NP_060184	NP_001153112 NP_001153113 NP_001276540 NP_780434
Location (UCSC)	Chr 20: 13.39 – 13.64 Mb	Chr 2: 139.83 – 140.07 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

Function

This gene encodes an endopeptidase that cleaves specific substrates following aspartate residues. The encoded protein undergoes posttranslational autoproteolytic processing to generate alpha and beta subunits, which reassemble into the active alpha2-beta2 heterotetramer. It is required to cleave MLL, a protein required for the maintenance of HOX gene expression, and TFIIA, a basal transcription factor. Cleavage of TFIIA has been found to drive spermatogenesis.[7]

Alternatively spliced transcript variants have been described, but their biological validity has not been determined.[6]

Clinical significance

Taspase1 is overexpressed in primary human cancers and functions as a non-oncogene addiction protease that coordinates cancer cell proliferation and apoptosis. Therefore, Taspase1 may serve as a novel anti-cancer therapeutic target.[8]

References

1. GRCh38: Ensembl release 89: ENSG00000089123 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000039033 - 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. Hsieh JJ, Cheng EH, Korsmeyer SJ (Nov 2003). "Taspase1: a threonine aspartase required for cleavage of MLL and proper HOX gene expression". Cell. 115 (3): 293–303. doi:10.1016/S0092-8674(03)00816-X. PMID 14636557. S2CID 18952302.
6. "Entrez Gene: TASP1 taspase, threonine aspartase, 1".
7. Oyama, T; Sasagawa, S; Takeda, S; Hess, R. A.; Lieberman, P. M.; Cheng, E. H.; Hsieh, J. J. (2013). "Cleavage of TFIIA by Taspase1 activates TRF2-specified mammalian male germ cell programs". Developmental Cell. 27 (2): 188–200. doi:10.1016/j.devcel.2013.09.025. PMC 3947863. PMID 24176642.
8. Chen DY, Liu H, Takeda S, Tu HC, Sasagawa S, Van Tine BA, Lu D, Cheng EH, Hsieh JJ (July 2010). "Taspase1 functions as a non-oncogene addiction protease that coordinates cancer cell proliferation and apoptosis". Cancer Res. 70 (13): 5358–67. doi:10.1158/0008-5472.CAN-10-0027. PMC 2909739. PMID 20516119.

Further reading

• Zhou H, Spicuglia S, Hsieh JJ, et al. (2006). "Uncleaved TFIIA is a substrate for taspase 1 and active in transcription". Mol. Cell. Biol. 26 (7): 2728–35. doi:10.1128/MCB.26.7.2728-2735.2006. PMC 1430320. PMID 16537915.
• Khan JA, Dunn BM, Tong L (2006). "Crystal structure of human Taspase1, a crucial protease regulating the function of MLL". Structure. 13 (10): 1443–52. doi:10.1016/j.str.2005.07.006. PMID 16216576.
• Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
• Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
• Hsieh JJ, Ernst P, Erdjument-Bromage H, et al. (2003). "Proteolytic cleavage of MLL generates a complex of N- and C-terminal fragments that confers protein stability and subnuclear localization". Mol. Cell. Biol. 23 (1): 186–94. doi:10.1128/MCB.23.1.186-194.2003. PMC 140678. PMID 12482972.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Deloukas P, Matthews LH, Ashurst J, et al. (2002). "The DNA sequence and comparative analysis of human chromosome 20". Nature. 414 (6866): 865–71. doi:10.1038/414865a. PMID 11780052.