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1.
Nature ; 615(7952): 535-540, 2023 03.
Artículo en Inglés | MEDLINE | ID: mdl-36859551

RESUMEN

Energy transfer from light-harvesting ketocarotenoids to the light-driven proton pump xanthorhodopsins has been previously demonstrated in two unique cases: an extreme halophilic bacterium1 and a terrestrial cyanobacterium2. Attempts to find carotenoids that bind and transfer energy to abundant rhodopsin proton pumps3 from marine photoheterotrophs have thus far failed4-6. Here we detected light energy transfer from the widespread hydroxylated carotenoids zeaxanthin and lutein to the retinal moiety of xanthorhodopsins and proteorhodopsins using functional metagenomics combined with chromophore extraction from the environment. The light-harvesting carotenoids transfer up to 42% of the harvested energy in the violet- or blue-light range to the green-light absorbing retinal chromophore. Our data suggest that these antennas may have a substantial effect on rhodopsin phototrophy in the world's lakes, seas and oceans. However, the functional implications of our findings are yet to be discovered.


Asunto(s)
Organismos Acuáticos , Procesos Fototróficos , Bombas de Protones , Rodopsinas Microbianas , Organismos Acuáticos/metabolismo , Organismos Acuáticos/efectos de la radiación , Bacterias/metabolismo , Bacterias/efectos de la radiación , Carotenoides/metabolismo , Color , Cianobacterias/metabolismo , Cianobacterias/efectos de la radiación , Procesos Heterotróficos/efectos de la radiación , Luz , Océanos y Mares , Procesos Fototróficos/efectos de la radiación , Bombas de Protones/metabolismo , Bombas de Protones/efectos de la radiación , Rodopsinas Microbianas/metabolismo , Rodopsinas Microbianas/efectos de la radiación , Zeaxantinas/metabolismo , Zeaxantinas/efectos de la radiación , Luteína/metabolismo , Luteína/efectos de la radiación , Metagenoma , Lagos
2.
Nature ; 621(7980): 711-715, 2023 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-37758892

RESUMEN

The nearby radio galaxy M87 offers a unique opportunity to explore the connections between the central supermassive black hole and relativistic jets. Previous studies of the inner region of M87 revealed a wide opening angle for the jet originating near the black hole1-4. The Event Horizon Telescope resolved the central radio source and found an asymmetric ring structure consistent with expectations from general relativity5. With a baseline of 17 years of observations, there was a shift in the jet's transverse position, possibly arising from an 8- to 10-year quasi-periodicity3. However, the origin of this sideways shift remains unclear. Here we report an analysis of radio observations over 22 years that suggests a period of about 11 years for the variation in the position angle of the jet. We infer that we are seeing a spinning black hole that induces the Lense-Thirring precession of a misaligned accretion disk. Similar jet precession may commonly occur in other active galactic nuclei but has been challenging to detect owing to the small magnitude and long period of the variation.

3.
Development ; 150(10)2023 05 15.
Artículo en Inglés | MEDLINE | ID: mdl-37218457

RESUMEN

Female insects can enter reproductive diapause, a state of suspended egg development, to conserve energy under adverse environments. In many insects, including the fruit fly, Drosophila melanogaster, reproductive diapause, also frequently called reproductive dormancy, is induced under low-temperature and short-day conditions by the downregulation of juvenile hormone (JH) biosynthesis in the corpus allatum (CA). In this study, we demonstrate that neuropeptide Diuretic hormone 31 (DH31) produced by brain neurons that project into the CA plays an essential role in regulating reproductive dormancy by suppressing JH biosynthesis in adult D. melanogaster. The CA expresses the gene encoding the DH31 receptor, which is required for DH31-triggered elevation of intracellular cAMP in the CA. Knocking down Dh31 in these CA-projecting neurons or DH31 receptor in the CA suppresses the decrease of JH titer, normally observed under dormancy-inducing conditions, leading to abnormal yolk accumulation in the ovaries. Our findings provide the first molecular genetic evidence demonstrating that CA-projecting peptidergic neurons play an essential role in regulating reproductive dormancy by suppressing JH biosynthesis.


Asunto(s)
Drosophila melanogaster , Hormonas de Insectos , Animales , Femenino , Corpora Allata , Drosophila melanogaster/genética , Drosophila melanogaster/fisiología , Hormonas Juveniles , Neuronas , Hormonas de Insectos/genética , Hormonas de Insectos/fisiología , Proteínas de Drosophila/genética , Proteínas de Drosophila/fisiología , Reproducción
4.
Med Mol Morphol ; 57(2): 147-154, 2024 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-38421457

RESUMEN

We report on single case of intraplacental choriocarcinoma (IC) coexisting with feto-maternal hemorrhage from our hospital, a rare malignant tumor that occurs in the chorionic villous trophoblast. To investigate genetic and epigenetic changes to the carcinogenesis of IC, we employed cancer gene panel analysis and whole methylation analysis from a recent case of IC. By Short Tandem Repeats analysis, we confirmed that the tumor of present IC was derived from concurrent normal chorionic villous trophoblast cells. No mutation was found in 145 cancer-related genes. Meanwhile, amplification in MDM2 gene was observed. Furthermore, we observed deferentially methylated CpG sites between tumor and surrounding normal placenta in present IC case. These observations suggest that IC might be arisen as a result of aberrations of methylation rather than of DNA mutations. Further studies are needed to clarify association between aberrant methylation and choriocarcinogenesis.


Asunto(s)
Coriocarcinoma , Metilación de ADN , Humanos , Femenino , Coriocarcinoma/genética , Coriocarcinoma/patología , Embarazo , Adulto , Neoplasias Uterinas/genética , Neoplasias Uterinas/patología , Repeticiones de Microsatélite/genética , Trofoblastos/patología , Trofoblastos/metabolismo , Placenta/patología , Islas de CpG/genética
5.
Biochemistry ; 61(23): 2698-2708, 2022 12 06.
Artículo en Inglés | MEDLINE | ID: mdl-36399519

RESUMEN

The proton transfer reaction belongs to one of the key triggers for the functional expression of membrane proteins. Rod and cone opsins are light-sensitive G-protein-coupled receptors (GPCRs) that undergo the cis-trans isomerization of the retinal chromophore in response to light. The isomerization event initiates a conformational change in the opsin protein moiety, which propagates the downstream effector signaling. The final step of receptor activation is the deprotonation of the retinal Schiff base, a proton transfer reaction which has been believed to be identical among the cone opsins. Here, we report an unexpected proton transfer reaction occurring in the early photoreaction process of primate blue-sensitive pigment (MB). By using low-temperature UV-visible spectroscopy, we found that the Lumi intermediate of MB formed in transition from the BL intermediate shows an absorption maximum in the UV region, indicating the deprotonation of the retinal Schiff base. Comparison of the light-induced difference FTIR spectra of Batho, BL, and Lumi showed significant α-helical backbone C=O stretching and protonated carboxylate C=O stretching vibrations only in the Lumi intermediate. The transition from BL to Lumi thus involves dramatic changes in protein environment with a proton transfer reaction between the Schiff base and the counterion resulting in an absorption maximum in the UV region.


Asunto(s)
Opsinas de los Conos , Pigmentos Retinianos , Animales , Pigmentos Retinianos/química , Protones , Bases de Schiff/química , Primates/metabolismo , Retinaldehído/química , Rodopsina/química
6.
Clin Exp Immunol ; 207(1): 95-103, 2022 01 28.
Artículo en Inglés | MEDLINE | ID: mdl-35020828

RESUMEN

Memory T cells are crucial players in vertebrate adaptive immunity but their development is incompletely understood. Here, we describe a method to produce human memory-like T cells from naive human T cells in culture. Using commercially available human T-cell differentiation kits, both purified naive CD8+ T cells and purified naive CD4+ T cells were activated via T-cell receptor signaling and appropriate cytokines for several days in culture. All the T-cell activators were then removed from the medium and the cultures were continued in hypoxic condition (1% O2 atmosphere) for several more days; during this period, most of the cells died, but some survived in a quiescent state for a month. The survivors had small round cell bodies, expressed differentiation markers characteristic of memory T cells and restarted proliferation when the T-cell activators were added back. We could also induce memory-like T cells from naive human T cells without hypoxia, if we froze the activated T cells or prepared the naive T cells from chilled filter buffy coats.


Asunto(s)
Linfocitos T CD4-Positivos , Memoria Inmunológica , Linfocitos T CD8-positivos , Diferenciación Celular , Humanos , Activación de Linfocitos
7.
Opt Express ; 30(9): 15616-15633, 2022 Apr 25.
Artículo en Inglés | MEDLINE | ID: mdl-35473278

RESUMEN

Brillouin optical correlation-domain sensing enables high-speed Brillouin gain spectrum (BGS) measurement at random positions along the optical fiber. To extract the Brillouin frequency shift (BFS) that reflects the real-time strain information, machine learning methods of principal components analysis (PCA) and support vector machine (SVM) are used in the signal processing for the BGSs. The performances of dimensionality reduction by PCA and SVM based on classification and regression are analyzed and compared. The experiment demonstrates an 8 kHz BGS acquisition repetition rate and an average BFS extraction time of 0.0104 ms, which is 27.3 times faster than the conventional method with no PCA. The proposed methods realize a real-time dynamic strain measurement at the frequency of 40 Hz.

8.
Stem Cells ; 39(11): 1435-1446, 2021 11.
Artículo en Inglés | MEDLINE | ID: mdl-34224650

RESUMEN

Although the physiological meaning of the high potential of mouse embryonic stem cells (ESCs) for meiotic entry is not understood, a rigid safeguarding system is required to prevent ectopic onset of meiosis. PRC1.6, a non-canonical PRC1, is known for its suppression of precocious and ectopic meiotic onset in germ cells and ESCs, respectively. MGA, a scaffolding component of PRC1.6, bears two distinct DNA-binding domains termed bHLHZ and T-box. However, it is unclear how this feature contributes to the functions of PRC1.6. Here, we demonstrated that both domains repress distinct sets of genes in murine ESCs, but substantial numbers of meiosis-related genes are included in both gene sets. In addition, our data demonstrated that bHLHZ is crucially involved in repressing the expression of Meiosin, which plays essential roles in meiotic entry with Stra8, revealing at least part of the molecular mechanisms that link negative and positive regulation of meiotic onset.


Asunto(s)
Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico , Meiosis , Células Madre Embrionarias de Ratones , Animales , Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico/metabolismo , ADN/metabolismo , Células Madre Embrionarias/metabolismo , Células Germinativas , Meiosis/genética , Ratones
9.
Curr Issues Mol Biol ; 44(1): 128-138, 2021 Dec 28.
Artículo en Inglés | MEDLINE | ID: mdl-35723389

RESUMEN

Primary aldosteronism is most often caused by aldosterone-producing adenoma (APA) and bi-lateral adrenal hyperplasia. Most APAs are caused by somatic mutations of various ion channels and pumps, the most common being the inward-rectifying potassium channel KCNJ5. Germ line mutations of KCNJ5 cause familial hyperaldosteronism type 3 (FH3), which is associated with severe hyperaldosteronism and hypertension. We present an unusual case of FH3 in a young woman, first diagnosed with primary aldosteronism at the age of 6 years, with bilateral adrenal hyperplasia, who underwent unilateral adrenalectomy (left adrenal) to alleviate hyperaldosteronism. However, her hyperaldosteronism persisted. At the age of 26 years, tomography of the remaining adrenal revealed two different adrenal tumors, one of which grew substantially in 4 months; therefore, the adrenal gland was removed. A comprehensive histological, immunohistochemical, and molecular evaluation of various sections of the adrenal gland and in situ visualization of aldosterone, using matrix-assisted laser desorption/ionization imaging mass spectrometry, was performed. Aldosterone synthase (CYP11B2) immunoreactivity was observed in the tumors and adrenal gland. The larger tumor also harbored a somatic ß-catenin activating mutation. Aldosterone visualized in situ was only found in the subcapsular regions of the adrenal and not in the tumors. Collectively, this case of FH3 presented unusual tumor development and histological/molecular findings.

10.
Opt Express ; 29(22): 35474-35489, 2021 Oct 25.
Artículo en Inglés | MEDLINE | ID: mdl-34808980

RESUMEN

The general neural networks (NNs) based on classification convert the Brillouin frequency shift (BFS) extraction in Brillouin-based distributed sensing to a problem in which the possible BFS output of the sensing system belongs to a finite number of discrete values. In this paper, we demonstrate a method of applying NNs with adaptive BFS incremental steps to signal processing for Brillouin optical correlation-domain sensing and achieve higher accuracy and operation speed. The comparison with the conventional curving fitting method shows that the NN improves the BFS measurement accuracy by 2-3 times and accelerates the signal processing speed by 1000 times for simulated signals. The experimental results demonstrate the NN provides 1.6-2.7 times enhancement for BFS measurement accuracy and 5000 times acceleration for the BFS extraction speed. This method supplies a potential solution to online signal processing for real-time Brillouin sensing.

11.
Opt Express ; 29(9): 13794-13805, 2021 Apr 26.
Artículo en Inglés | MEDLINE | ID: mdl-33985108

RESUMEN

We put forward a new theory on Brillouin optical correlation-domain reflectometry (BOCDR) based on arbitrary waveform modulation. We derive a universal representation for the spatial resolution using the foot convexity of the beat spectrum. This result well explains the previous results based on sinusoidal modulation, and thus our theory is the consistent extension of the conventional theory on BOCDR. This representation is also applicable to the spatial resolution evaluation of more complicated modulation schemes, such as the combined use of intensity and frequency modulations even with some phase delay. We also discuss what kinds of modulation waveforms should not be employed for distributed measurement to ensure high spatial resolution.

12.
Dev Growth Differ ; 63(4-5): 249-261, 2021 May.
Artículo en Inglés | MEDLINE | ID: mdl-34021588

RESUMEN

The corpora allata (CA) are essential endocrine organs that biosynthesize and secrete the sesquiterpenoid hormone, namely juvenile hormone (JH), to regulate a wide variety of developmental and physiological events in insects. CA are directly innervated with neurons in many insect species, implying the innervations to be important for regulating JH biosynthesis. Although this is also true for the model organism Drosophila melanogaster, neurotransmitters produced in the CA-projecting neurons are yet to be identified. In this study on D. melanogaster, we aimed to demonstrate that a subset of neurons producing the neuropeptide hugin, the invertebrate counterpart of the vertebrate neuromedin U, directly projects to the adult CA. A synaptic vesicle marker in the hugin neurons was observed at their axon termini located on the CA, which were immunolabeled with a newly-generated antibody to the JH biosynthesis enzyme JH acid O-methyltransferase. We also found the CA-projecting hugin neurons to likely express a gene encoding the specific receptor for diuretic hormone 44 (Dh44). Moreover, our data suggest that the CA-projecting hugin neurons have synaptic connections with the upstream neurons producing Dh44. Unexpectedly, the inhibition of CA-projecting hugin neurons did not significantly alter the expression levels of the JH-inducible gene Krüppel-homolog 1, which implies that the CA-projecting neurons are not involved in JH biosynthesis but rather in other known biological processes. This is the first study to identify a specific neurotransmitter of the CA-projecting neurons in D. melanogaster, and to anatomically characterize a neuronal pathway of the CA-projecting neurons and their upstream neurons.


Asunto(s)
Corpora Allata , Drosophila melanogaster , Animales , Diuréticos , Drosophila melanogaster/genética , Hormonas Juveniles , Neuronas
13.
Neurosurg Rev ; 44(3): 1591-1600, 2021 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-32671693

RESUMEN

Intracranial anaplastic hemangiopericytoma (AHPC) is a rare and malignant subset of solitary fibrous tumor/hemangiopericytoma (SFT/HPC) as per the WHO 2016 Classification of Tumors of the Central Nervous System. AHPC portends a poor prognosis and is associated with higher rates of recurrence/metastasis in comparison with SFT/HPC. Accordingly, it is critical to continue to define the clinical course of patients with AHPC and in so doing further refine clinicopathologic/immunohistochemical (IHC) criteria needed for definitive diagnosis. Herein, we describe clinical/histological characteristics of six patients with AHPC. In addition, we reviewed and analyzed the expression of various IHC markers reported within the literature (i.e., a total of 354 intracranial SFT/HPCs and 460 meningiomas). Histologically, tumors from our six patients were characterized by a staghorn-like vascular pattern, mitotic cells, and strong nuclear atypia. Immunohistochemically, all tumors displayed positive nuclear staining for STAT6; other markers, including CD34 and Bcl-2, were expressed only in three patients. Analysis of IHC expression patterns for SFT/HPC and meningioma within the literature revealed that nuclear expression of STAT6 had the highest specificity (100%) for SFT/HPC, followed by ALDH1 (97.2%) and CD34 (93.6%). Of note, SSTR2A (95.2%) and EMA (85%) displayed a high specificity for meningioma. Anaplastic SFT/HPC is a tumor with poor prognosis that is associated with higher rates of recurrence and metastasis in comparison with SFT/HPC. Given that anaplastic SFT/HPC requires more aggressive treatment than meningioma despite of a similar presentation on imaging, it is crucial to be able to distinguish between these tumors.


Asunto(s)
Biomarcadores de Tumor/metabolismo , Hemangiopericitoma/metabolismo , Neoplasias Meníngeas/metabolismo , Meningioma/metabolismo , Recurrencia Local de Neoplasia/metabolismo , Tumores Fibrosos Solitarios/metabolismo , Adulto , Anciano , Diagnóstico Diferencial , Femenino , Estudios de Seguimiento , Hemangiopericitoma/diagnóstico por imagen , Hemangiopericitoma/cirugía , Humanos , Masculino , Neoplasias Meníngeas/diagnóstico por imagen , Neoplasias Meníngeas/cirugía , Meningioma/diagnóstico por imagen , Meningioma/cirugía , Persona de Mediana Edad , Recurrencia Local de Neoplasia/diagnóstico por imagen , Recurrencia Local de Neoplasia/cirugía , Factor de Transcripción STAT6/metabolismo , Tumores Fibrosos Solitarios/diagnóstico por imagen , Tumores Fibrosos Solitarios/cirugía
14.
Opt Express ; 28(15): 21745-21748, 2020 Jul 20.
Artículo en Inglés | MEDLINE | ID: mdl-32752447

RESUMEN

This feature issue of Optics Express contains 17 articles expanding on recent advances in optical sensors presented at the eighth Asia-Pacific Optical Sensors Conference (APOS 2019) held in Auckland, New Zealand, from November 19 to 22, 2019. These articles span sensing for real-time positioning, refractive indices, strain, gas, and temperature using a variety of methods including photoacoustic computed tomography, coherent optical frequency-modulated continuous-wave interferometry, enhanced Bragg gratings, and phase-sensitive optical frequency-domain reflectometry.

15.
Med Mol Morphol ; 53(3): 131-140, 2020 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-32350620

RESUMEN

MicroRNAs (miRNAs) are a class of small noncoding RNAs that regulate gene expression. They play fundamental roles in several biological processes, including cell differentiation and proliferation, embryo development, organ development, and organ metabolism. Besides regulating the physiological processes, miRNAs regulate various pathological conditions such as tumors, metastases, metabolic diseases, and osteoporosis. Although several studies have been performed on miRNAs, only few studies have described the miRNA expression and functions in human reproductive tract tissues. During menstruation, the human endometrium undergoes extensive cyclic morphological and biochemical modifications before embryo implantation. In addition to the ovarian steroid hormones (estrogen and progesterone), endometrial autocrine or paracrine factors and embryo-derived signals play a significant role in endometrial functions. miRNAs are considered key regulators of gene expression in the human endometrium and implantation process, and their aberrant expression levels are associated with the development of various disorders, including tumorigenesis. In this review, we summarize the studies that show the role of miRNAs in regulating the physiological conditions of the endometrium and the implantation process and discuss the aberrant expression of miRNAs in ectopic pregnancy, endometriosis, and endometrial cancer.


Asunto(s)
Endometrio/metabolismo , Regulación de la Expresión Génica , MicroARNs/genética , Neoplasias Endometriales/genética , Vesículas Extracelulares/metabolismo , Femenino , Humanos , MicroARNs/metabolismo , Transporte de ARN/genética
16.
Dev Growth Differ ; 61(4): 283-293, 2019 May.
Artículo en Inglés | MEDLINE | ID: mdl-30919971

RESUMEN

It is thought that the spleen contains stem cells that differentiate into somatic cells other than immune cells. We investigated the presence of these hypothetical splenic cells with stem cell characteristics and identified adherent cells forming densely-packed colonies (Splenic Adherent Colony-forming Cell; SACC) in the spleen. Splenic Adherent Colony-forming Cell was positive for alkaline phosphatase staining and stage-specific embryonic antigen (SSEA)-1 antigen. However, the self-renewal properties of SACCs were limited because they stopped cell proliferation once colonies visible to the naked eye were formed. Gene expression analyses by semi-quantitative RT-PCR revealed the significant expression of c-Myc and Klf4, whereas faint or no expression was evident for Nanog, Oct3/4, and Sox2. Global expression analyses by DNA microarray and subsequent gene ontology analyses revealed that the expression levels of genes related to the immune system were significantly lower in SACCs than in control splenic cells. In contrast, genes unrelated to the immune system, such as those involved in cell adhesion and axon guidance, were relatively highly expressed in SACCs compared with control splenic cells. Taken together, we identified a novel cell type residing in the spleen that is different from the hypothetical splenic stem cell, but which bears some, but not all, characteristics that represent an undifferentiated state.


Asunto(s)
Adhesión Celular , Bazo/citología , Fosfatasa Alcalina/análisis , Animales , Proliferación Celular , Factor 4 Similar a Kruppel , Antígeno Lewis X/análisis , Ratones , Ratones Endogámicos C57BL , Ratas , Bazo/inmunología , Bazo/metabolismo
17.
Opt Lett ; 44(8): 2097-2100, 2019 Apr 15.
Artículo en Inglés | MEDLINE | ID: mdl-30985820

RESUMEN

We develop a new noise suppression technique to perform distributed strain and temperature sensing based on a higher-speed configuration of Brillouin optical correlation-domain reflectometry even when a polymer optical fiber (POF) is used as a sensing fiber. We acquire the spectral difference between with and without reference light, leading to selective observation of the beat signal of Brillouin-scattered light and reference light, which is effective for distributed sensing. After experimentally showing the usefulness of this technique, we demonstrate POF-based distributed temperature sensing and dynamic strain sensing.

18.
Stem Cells ; 36(9): 1355-1367, 2018 09.
Artículo en Inglés | MEDLINE | ID: mdl-29761578

RESUMEN

Embryonic stem cells (ESCs) exhibit two salient features beneficial for regenerative medicine: unlimited self-renewal and pluripotency. Methyl-CpG-binding domain protein 3 (Mbd3), a scaffolding component of the nucleosome remodeling deacetylase complex, is a specific regulator of pluripotency, as ESCs lacking Mbd3 are defective for lineage commitment potential but retain normal self-renewal properties. However, functional similarities and dissimilarities among the three Mbd3 isoforms (a, b, and c) have not been intensively explored. Herein, we demonstrated that Mbd3c, which lacks an entire portion of the MBD domain, exerted equivalent activity for counteracting the defective lineage commitment potential of Mbd3-knockout ESCs. Our analyses also revealed that the coiled-coil domain common to all three MBD3 isoforms, but not the MBD domain, plays a crucial role in this activity. Mechanistically, our data demonstrate that the activity of the coiled-coil domain is exerted, at least in part, through recruitment of polycomb repressive complex 2 to a subset of genes linked to development and organogenesis, thus establishing stable transcriptional repression. Stem Cells 2018;36:1355-1367.


Asunto(s)
Proteínas de Unión al ADN/metabolismo , Células Madre Embrionarias/metabolismo , Factores de Transcripción/metabolismo , Secuencia de Aminoácidos , Animales , Diferenciación Celular/fisiología , Células Cultivadas , Proteínas de Unión al ADN/química , Proteínas de Unión al ADN/genética , Células Madre Embrionarias/citología , Perfilación de la Expresión Génica , Técnicas de Inactivación de Genes , Ratones , Dominios Proteicos , Isoformas de Proteínas , Factores de Transcripción/química , Factores de Transcripción/genética
19.
PLoS Genet ; 12(1): e1005679, 2016 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-26741492

RESUMEN

Mitochondrial disorders have the highest incidence among congenital metabolic disorders characterized by biochemical respiratory chain complex deficiencies. It occurs at a rate of 1 in 5,000 births, and has phenotypic and genetic heterogeneity. Mutations in about 1,500 nuclear encoded mitochondrial proteins may cause mitochondrial dysfunction of energy production and mitochondrial disorders. More than 250 genes that cause mitochondrial disorders have been reported to date. However exact genetic diagnosis for patients still remained largely unknown. To reveal this heterogeneity, we performed comprehensive genomic analyses for 142 patients with childhood-onset mitochondrial respiratory chain complex deficiencies. The approach includes whole mtDNA and exome analyses using high-throughput sequencing, and chromosomal aberration analyses using high-density oligonucleotide arrays. We identified 37 novel mutations in known mitochondrial disease genes and 3 mitochondria-related genes (MRPS23, QRSL1, and PNPLA4) as novel causative genes. We also identified 2 genes known to cause monogenic diseases (MECP2 and TNNI3) and 3 chromosomal aberrations (6q24.3-q25.1, 17p12, and 22q11.21) as causes in this cohort. Our approaches enhance the ability to identify pathogenic gene mutations in patients with biochemically defined mitochondrial respiratory chain complex deficiencies in clinical settings. They also underscore clinical and genetic heterogeneity and will improve patient care of this complex disorder.


Asunto(s)
Exoma/genética , Heterogeneidad Genética , Mitocondrias/genética , Enfermedades Mitocondriales/genética , Adolescente , Niño , Preescolar , Aberraciones Cromosómicas , ADN Mitocondrial/genética , Femenino , Fibroblastos , Secuenciación de Nucleótidos de Alto Rendimiento , Humanos , Mutación INDEL/genética , Lactante , Recién Nacido , Masculino , Mitocondrias/patología , Enfermedades Mitocondriales/diagnóstico , Enfermedades Mitocondriales/patología , Polimorfismo de Nucleótido Simple/genética
20.
J Pediatr ; 193: 256-260, 2018 02.
Artículo en Inglés | MEDLINE | ID: mdl-29249525

RESUMEN

The diagnosis of Barth syndrome is challenging owing to the wide phenotypic spectrum with allelic heterogeneity. Here we report 3 cases of Barth syndrome with phenotypic and allelic heterogeneity that were diagnosed by different approaches, including whole exome sequencing and final confirmation by reverse-transcription polymease chain reaction.


Asunto(s)
Síndrome de Barth/diagnóstico , Factores de Transcripción/genética , Aciltransferasas , Síndrome de Barth/genética , Humanos , Lactante , Recién Nacido , Masculino , Mutación , Fenotipo , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa/métodos , Secuenciación del Exoma/métodos
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