Protein phosphatase 4 interacts with the Survival of Motor Neurons complex and enhances the temporal localisation of snRNPs (Publication with Expression of Concern. See vol. 135, 2022)

被引:50
作者
Carnegie, GK
Sleeman, JE
Morrice, N
Hastie, CJ
Peggie, MW
Philp, A
Lamond, AI
Cohen, PTW [1 ]
机构
[1] Univ Dundee, MRC, Prot Phosphorylat Unit, Div Cell Signalling, Dundee DD1 5EH, Scotland
[2] Univ Dundee, Sch Life Sci, Div Gene Regulat & Express, Dundee DD1 5EH, Scotland
关键词
Gemin4; Gemin3; spinal muscular atrophy; spliceosome; Cajal bodies (coiled bodies); snRNP;
D O I
10.1242/jcs.00409
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Protein phosphatase 4 (PPP4) is a ubiquitous essential protein serine/threonine phosphatase found in higher eukaryotes. Coordinate variation of the levels of the catalytic subunit (PPP4c) and the regulatory subunit (112) suggests that PPP4c and R2 form a heterodimeric core to which other regulatory subunits bind. Two proteins that specifically co-purify with Flag-epitope-tagged R2 expressed in HEK-293 cells were identified as Gemin3 and Gemin4. These two proteins have been identified previously as components of the Survival of Motor Neurons (SMN) protein complex, which is functionally defective in the hereditary disorder spinal muscular atrophy. Immunosedimentation of the epitope-tagged SMN protein complex from HeLa cells expressing CFP-SMN showed that the SMN protein interacts, as previously reported, with Gemin2 (SIP1), Gemin3 and Gemin4 and in addition associates with PPP4c. The SMN complex has been implicated in the assembly and maturation of small nuclear ribonucleoproteins (snRNPs). Expression of GFP-R2-PPP4c in HeLa cells enhances the temporal localisation of newly formed snRNPs, which is consistent with an association of R2-PPP4c with the SMN protein complex.
引用
收藏
页码:1905 / 1913
页数:9
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