排序方式: 共有104条查询结果,搜索用时 62 毫秒
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Grou CP Carvalho AF Pinto MP Alencastre IS Rodrigues TA Freitas MO Francisco T Sá-Miranda C Azevedo JE 《Cellular and molecular life sciences : CMLS》2009,66(2):254-262
The peroxisomal protein import machinery displays remarkable properties. Be it its capacity to accept already folded proteins
as substrates, its complex architecture or its energetics, almost every aspect of this machinery seems unique. The list of
unusual properties is still growing as shown by the recent finding that one of its central components, Pex5p, is transiently
monoubiquitinated at a cysteine residue. However, the data gathered in recent years also suggest that the peroxisomal import
machinery is not that exclusive and similarities with p97/Cdc48-mediated processes and with multisubunit RING-E3 ligases are
starting to emerge. Here, we discuss these data trying to distill the principles by which this complex machinery operates.
Received 16 July 2008; received after revision 25 August 2008; accepted 29 August 2008 相似文献
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Comino-Méndez I Gracia-Aznárez FJ Schiavi F Landa I Leandro-García LJ Letón R Honrado E Ramos-Medina R Caronia D Pita G Gómez-Graña A de Cubas AA Inglada-Pérez L Maliszewska A Taschin E Bobisse S Pica G Loli P Hernández-Lavado R Díaz JA Gómez-Morales M González-Neira A Roncador G Rodríguez-Antona C Benítez J Mannelli M Opocher G Robledo M Cascón A 《Nature genetics》2011,43(7):663-667
Hereditary pheochromocytoma (PCC) is often caused by germline mutations in one of nine susceptibility genes described to date, but there are familial cases without mutations in these known genes. We sequenced the exomes of three unrelated individuals with hereditary PCC (cases) and identified mutations in MAX, the MYC associated factor X gene. Absence of MAX protein in the tumors and loss of heterozygosity caused by uniparental disomy supported the involvement of MAX alterations in the disease. A follow-up study of a selected series of 59 cases with PCC identified five additional MAX mutations and suggested an association with malignant outcome and preferential paternal transmission of MAX mutations. The involvement of the MYC-MAX-MXD1 network in the development and progression of neural crest cell tumors is further supported by the lack of functional MAX in rat PCC (PC12) cells and by the amplification of MYCN in neuroblastoma and suggests that loss of MAX function is correlated with metastatic potential. 相似文献
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Unger S Böhm D Kaiser FJ Kaulfuss S Borozdin W Buiting K Burfeind P Böhm J Barrionuevo F Craig A Borowski K Keppler-Noreuil K Schmitt-Mechelke T Steiner B Bartholdi D Lemke J Mortier G Sandford R Zabel B Superti-Furga A Kohlhase J 《Nature genetics》2008,40(3):287-289
We identified four girls with a consistent constellation of facial dysmorphism and malformations previously reported in a single mother-daughter pair. Toe syndactyly, telecanthus and anogenital and renal malformations were present in all affected individuals; thus, we propose the name 'STAR syndrome' for this disorder. Using array CGH, qPCR and sequence analysis, we found causative mutations in FAM58A on Xq28 in all affected individuals, suggesting an X-linked dominant inheritance pattern for this recognizable syndrome. 相似文献
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Juan Francisco Araya 《Journal of Natural History》2015,49(29-30):1731-1761
A new introduced species, Otala punctata (Müller, 1774) and new records in Chile for Cornu aspersum (Müller, 1774) and Deroceras laeve (Müller, 1774) are documented based on surveys carried out in northern and central areas of the country. The presence and distribution of these alien species are complemented with a comprehensive compilation of all 34 non-indigenous species of marine, freshwater and terrestrial Mollusca in Chile; until 1999, only 16 alien species were known in Chile. Most of these alien species are found exclusively in transformed habitats, few exist in natural environments. The mechanism of introduction for the majority of these non-indigenous species is unknown; however, horticultural development, urban and suburban transformation of original natural habitats, and the aquarium trade are the most likely pathways of introduction. The highest threat of alien species is direct competition and predation of native molluscs, especially the small native land gastropods. Education and continuous field surveys are vital to detect and prevent their propagation as well as to avoid introduction of additional alien taxa. 相似文献
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Olga Moreno-Gonzalo Irene Fernandez-Delgado Francisco Sanchez-Madrid 《Cellular and molecular life sciences : CMLS》2018,75(1):1-19
Extracellular vesicles (EVs) are released by cells to the extracellular environment to mediate inter-cellular communication. Proteins, lipids, nucleic acids and metabolites shuttled in these vesicles modulate specific functions in recipient cells. The enrichment of selected sets of proteins in EVs compared with global cellular levels suggests the existence of specific sorting mechanisms to specify EV loading. Diverse post-translational modifications (PTMs) of proteins participate in the loading of specific elements into EVs. In this review, we offer a perspective on PTMs found in EVs and discuss the specific role of some PTMs, specifically Ubiquitin and Ubiquitin-like modifiers, in exosomal sorting of protein components. The understanding of these mechanisms will provide new strategies for biomedical applications. Examples include the presence of defined PTM marks on EVs as novel biomarkers for the diagnosis and prognosis of certain diseases, or the specific import of immunogenic components into EVs for vaccine generation. 相似文献
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Elisa Rossi Christilla Bachelot-Loza Dominique Pidard Pascale Gaussem Sonia Poirault-Chassac Francisco J. Blanco Carmen Langa Consuelo González-Manchón Jose M. Lopez Novoa David M. Smadja Carmelo Bernabeu 《Cellular and molecular life sciences : CMLS》2018,75(7):1269-1284
Complex interactions between platelets and activated endothelium occur during the thrombo-inflammatory reaction at sites of vascular injuries and during vascular hemostasis. The endothelial receptor endoglin is involved in inflammation through integrin-mediated leukocyte adhesion and transmigration; and heterozygous mutations in the endoglin gene cause hereditary hemorrhagic telangiectasia type 1. This vascular disease is characterized by a bleeding tendency that is postulated to be a consequence of telangiectasia fragility rather than a platelet defect, since platelets display normal functions in vitro in this condition. Here, we hypothesize that endoglin may act as an adhesion molecule involved in the interaction between endothelial cells and platelets through integrin recognition. We find that the extracellular domain of human endoglin promotes specific platelet adhesion under static conditions and confers resistance of adherent platelets to detachment upon exposure to flow. Also, platelets adhere to confluent endothelial cells in an endoglin-mediated process. Remarkably, Chinese hamster ovary cells ectopically expressing the human αIIbβ3 integrin acquire the capacity to adhere to myoblast transfectants expressing human endoglin, whereas platelets from Glanzmann’s thrombasthenia patients lacking the αIIbβ3 integrin are defective for endoglin-dependent adhesion to endothelial cells. Furthermore, the bleeding time, but not the prothrombin time, is significantly prolonged in endoglin-haplodeficient (Eng +/?) mice compared to Eng +/+ animals. These results suggest a new role for endoglin in αIIbβ3 integrin-mediated adhesion of platelets to the endothelium, and may provide a better understanding on the basic cellular mechanisms involved in hemostasis and thrombo-inflammatory events. 相似文献
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Groesser L Herschberger E Ruetten A Ruivenkamp C Lopriore E Zutt M Langmann T Singer S Klingseisen L Schneider-Brachert W Toll A Real FX Landthaler M Hafner C 《Nature genetics》2012,44(7):783-787
Nevus sebaceous is a common congenital cutaneous malformation. Affected individuals may develop benign and malignant secondary tumors in the nevi during life. Schimmelpenning syndrome is characterized by the association of nevus sebaceous with extracutaneous abnormalities. We report that of 65 sebaceous nevi studied, 62 (95%) had mutations in the HRAS gene and 3 (5%) had mutations in the KRAS gene. The HRAS c.37G>C mutation, which results in a p.Gly13Arg substitution, was present in 91% of lesions. Nonlesional tissues from 18 individuals had a wild-type sequence, confirming genetic mosaicism. The HRAS c.37G>C mutation was also found in 8 of 8 associated secondary tumors. Mosaicism for HRAS c.37G>C and KRAS c.35G>A mutations was found in two individuals with Schimmelpenning syndrome. Functional analysis of HRAS c.37G>C mutant cells showed constitutive activation of the MAPK and PI3K-Akt signaling pathways. Our results indicate that nevus sebaceous and Schimmelpenning syndrome are caused by postzygotic HRAS and KRAS mutations. These mutations may predispose individuals to the development of secondary tumors in nevus sebaceous. 相似文献
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