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2.
Exp Hematol ; 72: 1-8, 2019 04.
Artigo em Inglês | MEDLINE | ID: mdl-30639577

RESUMO

Ubiquitin-specific protease 44 (USP44) is a nuclear protein with deubiquitinase (DUB) catalytic activity that has been implicated as an important regulator of cell cycle progression, gene expression, and genomic stability. Dysregulation in the molecular machinery controlling cell proliferation, gene expression, and genomic stability in human or mouse is commonly linked to hematopoietic dysfunction, immunodeficiency, and cancer. We therefore set out to explore the role of USP44 in hematopoietic and immune systems through characterization of a Usp44-deficient mouse model. We report that USP44 is dispensable for the maintenance of hematopoietic stem cell numbers and function under homeostatic conditions, and also after irradiation or serial transplantation. USP44 is also not required for normal lymphocyte development. Usp44-deficient B cells show normal activation, proliferation, and immunoglobulin class switching in response to in vitro stimulation, and Usp44-deficient mice mount normal antibody response to immunization. We also tested the effects of USP44 deficiency on disease progression and survival in the Emu-myc model of mouse B-cell lymphoma and observed a trend toward earlier lethality of Usp44-/- Emu-myc mice; however, this did not reach statistical significance. Overall, we conclude that USP44 is dispensable for the normal physiology of hematopoietic and immune systems, and its functions in these systems are likely redundant with other USP family proteins.


Assuntos
Linfócitos B/imunologia , Hematopoese/imunologia , Células-Tronco Hematopoéticas/imunologia , Imunidade Celular , Linfoma de Células B/imunologia , Neoplasias Experimentais/imunologia , Ubiquitina Tiolesterase/imunologia , Animais , Formação de Anticorpos/genética , Linfócitos B/patologia , Linhagem Celular , Proliferação de Células , Hematopoese/genética , Células-Tronco Hematopoéticas/patologia , Linfoma de Células B/genética , Linfoma de Células B/patologia , Camundongos , Camundongos Knockout , Neoplasias Experimentais/genética , Neoplasias Experimentais/patologia , Ubiquitina Tiolesterase/genética
3.
J Biol Chem ; 293(23): 8861-8873, 2018 06 08.
Artigo em Inglês | MEDLINE | ID: mdl-29669809

RESUMO

Integral membrane proteins are prone to aggregation and misfolding in aqueous environments and therefore require binding by molecular chaperones during their biogenesis. Chloroplast signal recognition particle 43 (cpSRP43) is an ATP-independent chaperone required for the biogenesis of the most abundant class of membrane proteins, the light-harvesting chlorophyll a/b-binding proteins (LHCPs). Previous work has shown that cpSRP43 specifically recognizes an L18 loop sequence conserved among LHCP paralogs. However, how cpSRP43 protects the transmembrane domains (TMDs) of LHCP from aggregation was unclear. In this work, alkylation-protection and site-specific cross-linking experiments found that cpSRP43 makes extensive contacts with all the TMDs in LHCP. Site-directed mutagenesis identified a class of cpSRP43 mutants that bind tightly to the L18 sequence but are defective in chaperoning full-length LHCP. These mutations mapped to hydrophobic surfaces on or near the bridging helix and the ß-hairpins lining the ankyrin repeat motifs of cpSRP43, suggesting that these regions are potential sites for interaction with the client TMDs. Our results suggest a working model for client protein interactions in this membrane protein chaperone.


Assuntos
Proteínas de Arabidopsis/metabolismo , Arabidopsis/metabolismo , Proteínas de Ligação à Clorofila/metabolismo , Complexo de Proteína do Fotossistema II/metabolismo , Mapas de Interação de Proteínas , Partícula de Reconhecimento de Sinal/metabolismo , Arabidopsis/química , Arabidopsis/genética , Proteínas de Arabidopsis/química , Proteínas de Arabidopsis/genética , Proteínas de Ligação à Clorofila/química , Modelos Moleculares , Complexo de Proteína do Fotossistema II/química , Mutação Puntual , Agregados Proteicos , Conformação Proteica , Domínios e Motivos de Interação entre Proteínas , Partícula de Reconhecimento de Sinal/química , Partícula de Reconhecimento de Sinal/genética
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