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https://www.readbyqxmd.com/read/30300710/two-siblings-with-a-novel-nonsense-variant-provide-further-delineation-of-the-spectrum-of-recessive-klhl7-diseases
#1
Lauren Jeffries, Jordan E Olivieri, Weizhen Ji, Michele Spencer-Manzon, Allen Bale, Monica Konstantino, Saquib A Lakhani
Mutations in Kelch-like family member 7 (KLHL7) have recently been described as a cause of a constellation of clinical findings with descriptions of both a Crisponi syndrome (CS)/cold-induced sweating syndrome type 1 (CISS1)-like, as well as a Bohring-Opitz syndrome (BOS)-like presentation. Here we report two siblings of Guatelmalan descent with a novel homozygous nonsense mutation (p.Arg326*) in KLHL7. These children have multiple dysmorphic features and developmental delay. Interestingly, their clinical traits inconsistently overlap both the CS/CISS1-like and BOS-like phenotypes, and the siblings also have subtle differences from each other, suggesting that clinicians need to be aware of the degree of variability in the presentations of these patients...
October 6, 2018: European Journal of Medical Genetics
https://www.readbyqxmd.com/read/30142437/bi-allelic-c-181_183deltgt-in-btb-domain-of-klhl7-is-associated-with-overlapping-phenotypes-of-crisponi-ciss1-like-and-bohring-opitz-like-syndrome
#2
Anil Kanthi, Malavika Hebbar, Stephanie L Bielas, Katta M Girisha, Anju Shukla
Biallelic pathogenic variants in KLHL7 are known to result in Crisponi syndrome (CS)/cold-induced sweating syndrome type 1 (CISS1) like phenotype and Bohring-Opitz-like syndrome. In this report, a trio whole-exome sequencing (WES) was performed in proband with cold-induced sweating, microcephaly, facial dysmorphism, spasticity, failure to thrive, pigmentary abnormalities of the retina, hypoplasia of corpus callosum and periventricular nodular heterotopia. A novel homozygous in-frame deletion was identified in exon 2 of KLHL7, affecting the BTB domain of the protein...
August 22, 2018: European Journal of Medical Genetics
https://www.readbyqxmd.com/read/29625027/bi-allelic-mutations-in-klhl7-cause-a-crisponi-ciss1-like-phenotype-associated-with-early-onset-retinitis-pigmentosa
#3
Andrea Angius, Paolo Uva, Insa Buers, Manuela Oppo, Alessandro Puddu, Stefano Onano, Ivana Persico, Angela Loi, Loredana Marcia, Wolfgang Höhne, Gianmauro Cuccuru, Giorgio Fotia, Manila Deiana, Mara Marongiu, Hatice Tuba Atalay, Sibel Inan, Osama El Assy, Leo M E Smit, Ilyas Okur, Koray Boduroglu, Gülen Eda Utine, Esra Kılıç, Giuseppe Zampino, Giangiorgio Crisponi, Laura Crisponi, Frank Rutsch
No abstract text is available yet for this article.
April 5, 2018: American Journal of Human Genetics
https://www.readbyqxmd.com/read/29435412/mirnaexpression-profile-of-retinal-pigment-epithelial-cells-under-oxidative-stress-conditions
#4
Luigi Donato, Placido Bramanti, Concetta Scimone, Carmela Rinaldi, Rosalia D'Angelo, Antonina Sidoti
Deep analysis of regulative mechanisms of transcription and translation in eukaryotes could improve knowledge of many genetic pathologies such as retinitis pigmentosa (RP). New layers of complexity have recently emerged with the discovery that 'junk' DNA is transcribed and, among these, miRNAs have assumed a preponderant role. We compared changes in the expression of miRNAs obtained from whole transcriptome analyses, between two groups of retinal pigment epithelium (RPE) cells, one untreated and the other exposed to the oxidant agent oxidized low-density lipoprotein (oxLDL), examining four time points (1, 2, 4 and 6 h)...
February 2018: FEBS Open Bio
https://www.readbyqxmd.com/read/29074562/expanding-the-clinical-spectrum-of-recessive-truncating-mutations-of-klhl7-to-a-bohring-opitz-like-phenotype
#5
Ange-Line Bruel, Stefania Bigoni, Joanna Kennedy, Margo Whiteford, Chris Buxton, Giulia Parmeggiani, Matt Wherlock, Geoff Woodward, Mark Greenslade, Maggie Williams, Judith St-Onge, Alessandra Ferlini, Giampaolo Garani, Elisa Ballardini, Bregje W van Bon, Rocio Acuna-Hidalgo, Axel Bohring, Jean-François Deleuze, Anne Boland, Vincent Meyer, Robert Olaso, Emmanuelle Ginglinger, Ddd Study, Jean-Baptiste Rivière, Han G Brunner, Alexander Hoischen, Ruth Newbury-Ecob, Laurence Faivre, Christel Thauvin-Robinet, Julien Thevenon
BACKGROUND: Bohring-Opitz syndrome (BOS) is a rare genetic disorder characterised by a recognisable craniofacial appearance and a typical 'BOS' posture. BOS is caused by sporadic mutations of ASXL1 . However, several typical patients with BOS have no molecular diagnosis, suggesting clinical and genetic heterogeneity. OBJECTIVES: To expand the phenotypical spectrum of autosomal recessive variants of KLHL7 , reported as causing Crisponi syndrome/cold-induced sweating syndrome type 1 (CS/CISS1)-like syndrome...
December 2017: Journal of Medical Genetics
https://www.readbyqxmd.com/read/29032201/klhl7-promotes-tut1-ubiquitination-associated-with-nucleolar-integrity-implications-for-retinitis-pigmentosa
#6
Jaehyun Kim, Fuminori Tsuruta, Tomomi Okajima, Sarasa Yano, Ban Sato, Tomoki Chiba
Kelch-like protein 7 (KLHL7) is a component of Cul3-based Cullin-RING ubiquitin ligase. Recent studies have revealed that mutations in klhl7 gene cause several disorders, such as retinitis pigmentosa (RP). Although KLHL7 is considered to be crucial for regulating the protein homeostasis, little is known about its biological functions. In this study, we report that KLHL7 increases terminal uridylyl transferase 1 (TUT1) ubiquitination involved in nucleolar integrity. TUT1 is normally localized in nucleolus; however, expression of KLHL7 facilitates a vulnerability of nucleolar integrity, followed by a decrease of TUT1 localization in nucleolus...
December 9, 2017: Biochemical and Biophysical Research Communications
https://www.readbyqxmd.com/read/28391543/increased-brain-expression-of-gpnmb-is-associated-with-genome-wide-significant-risk-for-parkinson-s-disease-on-chromosome-7p15-3
#7
Megha N Murthy, Cornelis Blauwendraat, Sebastian Guelfi, John Hardy, Patrick A Lewis, Daniah Trabzuni
Genome wide association studies (GWAS) for Parkinson's disease (PD) have previously revealed a significant association with a locus on chromosome 7p15.3, initially designated as the glycoprotein non-metastatic melanoma protein B (GPNMB) locus. In this study, the functional consequences of this association on expression were explored in depth by integrating different expression quantitative trait locus (eQTL) datasets (Braineac, CAGEseq, GTEx, and Phenotype-Genotype Integrator (PheGenI)). Top risk SNP rs199347 eQTLs demonstrated increased expressions of GPNMB, KLHL7, and NUPL2 with the major allele (AA) in brain, with most significant eQTLs in cortical regions, followed by putamen...
July 2017: Neurogenetics
https://www.readbyqxmd.com/read/27392078/bi-allelic-mutations-in-klhl7-cause-a-crisponi-ciss1-like-phenotype-associated-with-early-onset-retinitis-pigmentosa
#8
Andrea Angius, Paolo Uva, Insa Buers, Manuela Oppo, Alessandro Puddu, Stefano Onano, Ivana Persico, Angela Loi, Loredana Marcia, Wolfgang Höhne, Gianmauro Cuccuru, Giorgio Fotia, Manila Deiana, Mara Marongiu, Hatice Tuba Atalay, Sibel Inan, Osama El Assy, Leo M E Smit, Ilyas Okur, Koray Boduroglu, Gülen Eda Utine, Esra Kılıç, Giuseppe Zampino, Giangiorgio Crisponi, Laura Crisponi, Frank Rutsch
Crisponi syndrome (CS)/cold-induced sweating syndrome type 1 (CISS1) is a very rare autosomal-recessive disorder characterized by a complex phenotype with high neonatal lethality, associated with the following main clinical features: hyperthermia and feeding difficulties in the neonatal period, scoliosis, and paradoxical sweating induced by cold since early childhood. CS/CISS1 can be caused by mutations in cytokine receptor-like factor 1 (CRLF1). However, the physiopathological role of CRLF1 is still poorly understood...
July 7, 2016: American Journal of Human Genetics
https://www.readbyqxmd.com/read/26321861/new-col6a6-variant-detected-by-whole-exome-sequencing-is-linked-to-break-points-in-intron-4-and-3-utr-deleting-exon-5-of-rho-and-causing-adrp
#9
Miguel de Sousa Dias, Imma Hernan, Barbara Delás, Beatriz Pascual, Emma Borràs, Maria José Gamundi, Begoña Mañé, Patricia Fernández-San José, Carmen Ayuso, Miguel Carballo
PURPOSE: This study aimed to test a newly devised cost-effective multiplex PCR assay for the molecular diagnosis of autosomal dominant retinitis pigmentosa (adRP), as well as the use of whole-exome sequencing (WES) to detect disease-causing mutations in adRP. METHODS: Genomic DNA was extracted from peripheral blood lymphocytes of index patients with adRP and their affected and unaffected family members. We used a newly devised multiplex PCR assay capable of amplifying the genetic loci of RHO, PRPH2, RP1, PRPF3, PRPF8, PRPF31, IMPDH1, NRL, CRX, KLHL7, and NR2E3 to molecularly diagnose 18 index patients with adRP...
2015: Molecular Vision
https://www.readbyqxmd.com/read/25584925/a-genome-wide-association-study-of-chronic-obstructive-pulmonary-disease-in-hispanics
#10
MULTICENTER STUDY
Wei Chen, John M Brehm, Ani Manichaikul, Michael H Cho, Nadia Boutaoui, Qi Yan, Kristin M Burkart, Paul L Enright, Jerome I Rotter, Hans Petersen, Shuguang Leng, Ma'en Obeidat, Yohan Bossé, Corry-Anke Brandsma, Ke Hao, Stephen S Rich, Rhea Powell, Lydiana Avila, Manuel Soto-Quiros, Edwin K Silverman, Yohannes Tesfaigzi, R Graham Barr, Juan C Celedón
RATIONALE: Genome-wide association studies (GWAS) of chronic obstructive pulmonary disease (COPD) have identified disease-susceptibility loci, mostly in subjects of European descent. OBJECTIVES: We hypothesized that by studying Hispanic populations we would be able to identify unique loci that contribute to COPD pathogenesis in Hispanics but remain undetected in GWAS of non-Hispanic populations. METHODS: We conducted a metaanalysis of two GWAS of COPD in independent cohorts of Hispanics in Costa Rica and the United States (Multi-Ethnic Study of Atherosclerosis [MESA])...
March 2015: Annals of the American Thoracic Society
https://www.readbyqxmd.com/read/24803682/label-free-real-time-detection-of-the-dynamic-processes-of-protein-degradation-using-oblique-incidence-reflectivity-difference-method
#11
S Liu, J H Zhu, L P He, J Dai, H B Lu, L Wu, K J Jin, G Z Yang, H Zhu
Based on the requirements for studying the dynamic process of proteinase action substrates in life science, we selected six random proteins including 1L-10, SCGB2A2, CENPQ, GST, HK1, KLHL7, as well as five different concentrations of 1L-10 proteins of 1 mg/ml, 0.5 mg/ml, 0.25 mg/ml, 0.125 mg/ml, and 0.0625 mg/ml, and fabricated two types of substrate protein microarrays, respectively. We detected the dynamic processes of proteins degraded by proteinase K using oblique-incidence reflectivity difference (OIRD) method in a label-free and real-time manner...
April 21, 2014: Applied Physics Letters
https://www.readbyqxmd.com/read/23950152/prevalence-of-mutations-in-eyegene-probands-with-a-diagnosis-of-autosomal-dominant-retinitis-pigmentosa
#12
COMPARATIVE STUDY
Lori S Sullivan, Sara J Bowne, Melissa J Reeves, Delphine Blain, Kerry Goetz, Vida Ndifor, Sally Vitez, Xinjing Wang, Santa J Tumminia, Stephen P Daiger
PURPOSE: To screen samples from patients with presumed autosomal dominant retinitis pigmentosa (adRP) for mutations in 12 disease genes as a contribution to the research and treatment goals of the National Ophthalmic Disease Genotyping and Phenotyping Network (eyeGENE). METHODS: DNA samples were obtained from eyeGENE. A total of 170 probands with an intake diagnosis of adRP were tested through enrollment in eyeGENE. The 10 most common genes causing adRP (IMPDH1, KLHL7, NR2E3, PRPF3/RP18, PRPF31/RP11, PRPF8/RP13, PRPH2/RDS, RHO, RP1, and TOPORS) were chosen for PCR-based dideoxy sequencing, along with the two X-linked RP genes, RPGR and RP2...
September 19, 2013: Investigative Ophthalmology & Visual Science
https://www.readbyqxmd.com/read/23848512/exploring-signatures-of-positive-selection-in-pigmentation-candidate-genes-in-populations-of-east-asian-ancestry
#13
Jessica L Hider, Rachel M Gittelman, Tapan Shah, Melissa Edwards, Arnold Rosenbloom, Joshua M Akey, Esteban J Parra
BACKGROUND: Currently, there is very limited knowledge about the genes involved in normal pigmentation variation in East Asian populations. We carried out a genome-wide scan of signatures of positive selection using the 1000 Genomes Phase I dataset, in order to identify pigmentation genes showing putative signatures of selective sweeps in East Asia. We applied a broad range of methods to detect signatures of selection including: 1) Tests designed to identify deviations of the Site Frequency Spectrum (SFS) from neutral expectations (Tajima's D, Fay and Wu's H and Fu and Li's D* and F*), 2) Tests focused on the identification of high-frequency haplotypes with extended linkage disequilibrium (iHS and Rsb) and 3) Tests based on genetic differentiation between populations (LSBL)...
2013: BMC Evolutionary Biology
https://www.readbyqxmd.com/read/23349464/structural-basis-for-cul3-protein-assembly-with-the-btb-kelch-family-of-e3-ubiquitin-ligases
#14
Peter Canning, Christopher D O Cooper, Tobias Krojer, James W Murray, Ashley C W Pike, Apirat Chaikuad, Tracy Keates, Chancievan Thangaratnarajah, Viktorija Hojzan, Vikram Ayinampudi, Brian D Marsden, Opher Gileadi, Stefan Knapp, Frank von Delft, Alex N Bullock
Cullin-RING ligases are multisubunit E3 ubiquitin ligases that recruit substrate-specific adaptors to catalyze protein ubiquitylation. Cul3-based Cullin-RING ligases are uniquely associated with BTB adaptors that incorporate homodimerization, Cul3 assembly, and substrate recognition into a single multidomain protein, of which the best known are BTB-BACK-Kelch domain proteins, including KEAP1. Cul3 assembly requires a BTB protein "3-box" motif, analogous to the F-box and SOCS box motifs of other Cullin-based E3s...
March 15, 2013: Journal of Biological Chemistry
https://www.readbyqxmd.com/read/22084217/phenotypic-characterization-of-3-families-with-autosomal-dominant-retinitis-pigmentosa-due-to-mutations-in-klhl7
#15
Yuquan Wen, Kirsten G Locke, Martin Klein, Sara J Bowne, Lori S Sullivan, Joseph W Ray, Stephen P Daiger, David G Birch, Dianna K Hughbanks-Wheaton
OBJECTIVE: To characterize the visual phenotype caused by mutations in the BTB-Kelch protein, KLHL7, responsible for the RP42 form of autosomal dominant retinitis pigmentosa (RP). METHODS: Comprehensive ophthalmic testing included visual acuity, static visual field, kinetic visual field, dark adaptometry, full-field electroretinography, spectral-domain optical coherence tomography, and fundus photography. Longitudinal visual function data (range, 15-27 years) were available for some of the affected individuals...
November 2011: Archives of Ophthalmology
https://www.readbyqxmd.com/read/21828050/ubiquitin-ligase-activity-of-cul3-klhl7-protein-is-attenuated-by-autosomal-dominant-retinitis-pigmentosa-causative-mutation
#16
Yu Kigoshi, Fuminori Tsuruta, Tomoki Chiba
Substrate-specific protein degradation mediated by the ubiquitin proteasome system (UPS) is crucial for the proper function of the cell. Proteins are specifically recognized and ubiquitinated by the ubiquitin ligases (E3s) and are then degraded by the proteasome. BTB proteins act as the substrate recognition subunit that recruits their cognate substrates to the Cullin 3-based multisubunit E3s. Recently, it was reported that missense mutations in KLHL7, a BTB-Kelch protein, are related to autosomal dominant retinitis pigmentosa (adRP)...
September 23, 2011: Journal of Biological Chemistry
https://www.readbyqxmd.com/read/20547956/phenotype-associated-with-mutation-in-the-recently-identified-autosomal-dominant-retinitis-pigmentosa-klhl7-gene
#17
Therése Hugosson, James S Friedman, Vesna Ponjavic, Magnus Abrahamson, Anand Swaroop, Sten Andréasson
OBJECTIVE: To characterize the clinical phenotype, with an emphasis on electrophysiologic findings, in a family with autosomal dominant retinitis pigmentosa caused by mutation in the recently identified KLHL7 gene. METHODS: Eleven patients from a single family were selected from the Swedish retinitis pigmentosa register. Four patients had been examined 13 to 17 years earlier and underwent further ophthalmologic examination, including visual acuity, fundus inspection, Goldmann perimetry, full-field electroretinography (ERG), multifocal ERG, and optical coherence tomography...
June 2010: Archives of Ophthalmology
https://www.readbyqxmd.com/read/19520207/mutations-in-a-btb-kelch-protein-klhl7-cause-autosomal-dominant-retinitis-pigmentosa
#18
James S Friedman, Joseph W Ray, Naushin Waseem, Kory Johnson, Matthew J Brooks, Therése Hugosson, Debra Breuer, Kari E Branham, Daniel S Krauth, Sara J Bowne, Lori S Sullivan, Vesna Ponjavic, Lotta Gränse, Ritu Khanna, Edward H Trager, Linn M Gieser, Dianna Hughbanks-Wheaton, Radu I Cojocaru, Noor M Ghiasvand, Christina F Chakarova, Magnus Abrahamson, Harald H H Göring, Andrew R Webster, David G Birch, Goncalo R Abecasis, Yang Fann, Shomi S Bhattacharya, Stephen P Daiger, John R Heckenlively, Sten Andréasson, Anand Swaroop
Retinitis pigmentosa (RP) refers to a genetically heterogeneous group of progressive neurodegenerative diseases that result in dysfunction and/or death of rod and cone photoreceptors in the retina. So far, 18 genes have been identified for autosomal-dominant (ad) RP. Here, we describe an adRP locus (RP42) at chromosome 7p15 through linkage analysis in a six-generation Scandinavian family and identify a disease-causing mutation, c.449G-->A (p.S150N), in exon 6 of the KLHL7 gene. Mutation screening of KLHL7 in 502 retinopathy probands has revealed three different missense mutations in six independent families...
June 2009: American Journal of Human Genetics
https://www.readbyqxmd.com/read/19128516/a-gene-expression-signature-shared-by-human-mature-oocytes-and-embryonic-stem-cells
#19
COMPARATIVE STUDY
Said Assou, Doris Cerecedo, Sylvie Tondeur, Véronique Pantesco, Outi Hovatta, Bernard Klein, Samir Hamamah, John De Vos
BACKGROUND: The first week of human pre-embryo development is characterized by the induction of totipotency and then pluripotency. The understanding of this delicate process will have far reaching implication for in vitro fertilization and regenerative medicine. Human mature MII oocytes and embryonic stem (ES) cells are both able to achieve the feat of cell reprogramming towards pluripotency, either by somatic cell nuclear transfer or by cell fusion, respectively. Comparison of the transcriptome of these two cell types may highlight genes that are involved in pluripotency initiation...
2009: BMC Genomics
https://www.readbyqxmd.com/read/16918702/detection-of-autoantibodies-to-the-btb-kelch-protein-klhl7-in-cancer-sera
#20
COMPARATIVE STUDY
G Bredholt, A Storstein, M Haugen, B K Krossnes, E Husebye, P Knappskog, C A Vedeler
The aim of the study was to search for novel targets of autoantibodies in patients with paraneoplastic neurological syndromes (PNS). PNS are mediated by immune reactions against autoantigen(s) shared by the cancer cells and the nervous system. By serological screening of a rat cerebellum cDNA expression library using anti-Hu-positive sera from three patients with paraneoplastic encephalomyelitis (PEM), we identified an open reading frame encoding an isoform of the BTB-kelch protein KLHL7. Immunohistochemical studies demonstrated that the KLHL7 protein is expressed in the nuclei of neurones, but not in other tissues including various cancers...
September 2006: Scandinavian Journal of Immunology
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