keyword
https://read.qxmd.com/read/37656279/a-founder-dbr1-variant-causes-a-lethal-form-of-congenital-ichthyosis
#21
JOURNAL ARTICLE
Hanan E Shamseldin, Mukunth Sadagopan, Javier Martini, Ruslan Al-Ali, Mandy Radefeldt, Mojgan Ataei, Sabrina Lemke, Zuhair Rahbeeni, Fuad Al Mutairi, Faroug Ababneh, Hadeel A AlRukban, Firdous Abdulwahab, Saleh Mohammed Alhajj, Peter Bauer, Aida Bertoli-Avella, Fowzan S Alkuraya
DBR1 encodes the only known human lariat debranching enzyme and its deficiency has been found to cause an autosomal recessive inborn error of immunity characterized by pediatric brainstem viral-induced encephalitis (MIM 619441). We describe a distinct allelic disorder caused by a founder recessive DBR1 variant in four families (DBR1(NM_016216.4):c.200A > G (p.Tyr67Cys)). Consistent features include prematurity, severe intrauterine growth deficiency, congenital ichthyosis-like presentation (collodion membrane, severe skin peeling and xerosis), and death before the first year of life...
October 2023: Human Genetics
https://read.qxmd.com/read/37572568/meta-analysis-of-the-outcomes-of-peri-device-leak-after-left-atrial-appendage-closure
#22
JOURNAL ARTICLE
Mostafa Reda Mostafa, Mohamed Magdi Eid, Mohamed Abuelazm, Ahmad Al-Abdouh, Mostafa Najim, Abdul Rhman Hassan, Amro A El-Sakka, Sarath Lal Mannumbeth Renjithal, Muhammad Ahmed Malik, Sarah Mohamed, Mallory Balmer-Swain, Timir K Paul, Andrew M Goldsweig
Left atrial appendage closure (LAAC) reduces the risk of thromboembolic stroke in atrial fibrillation. Peri-device leak (PDL) after LAAC may affect the subsequent risk of thromboembolism. We conducted a systematic review and meta-analysis to evaluate the effect of PDL after LAAC. We searched PubMed/Medline, Embase, and Google Scholar for studies reporting outcomes of PDL after LAAC from inception through October 2022. The primary outcome was the composite of stroke, transient ischemic attack (TIA), or systemic embolism (SE)...
August 10, 2023: American Journal of Cardiology
https://read.qxmd.com/read/37565610/-it-s-not-safe-for-me-and-what-would-it-achieve-acceptability-of-patient-referral-partner-notification-for-sexually-transmitted-infections-to-young-people-a-mixed-methods-study-from-zimbabwe
#23
JOURNAL ARTICLE
Joni Lariat, Chido Dziva Chikwari, Ethel Dauya, Valentine T Baumu, Victor Kaisi, Laura Kafata, Esnath Meza, Victoria Simms, Constance Mackworth-Young, Helena Rochford, Anna Machiha, Tsitsi Bandason, Suzanna C Francis, Rashida A Ferrand, Sarah Bernays
Partner notification (PN) is considered integral to the management of sexually transmitted infections (STI). Patient-referral is a common PN strategy and relies on index cases notifying and encouraging their partners to access treatment; however, it has shown limited efficacy. We conducted a mixed methods study to understand young people's experiences of PN, particularly the risks and challenges encountered during patient-referral. All young people (16-24 years) attending a community-based sexual and reproductive health service in Zimbabwe who were diagnosed with an STI were counselled and offered PN slips, which enabled their partners to access free treatment at the service...
December 2023: Sexual and reproductive health matters
https://read.qxmd.com/read/37554968/circular-stable-intronic-rnas-possess-distinct-biological-features-and-are-deregulated-in-bladder-cancer
#24
JOURNAL ARTICLE
Asta M Rasmussen, Trine Line H Okholm, Michael Knudsen, Søren Vang, Lars Dyrskjøt, Thomas B Hansen, Jakob S Pedersen
Until recently, intronic lariats were regarded as short-lasting splicing byproducts with no apparent function; however, increasing evidence of stable derivatives suggests regulatory roles. Yet little is known about their characteristics, functions, distribution, and expression in healthy and tumor tissue. Here, we profiled and characterized circular stable intronic sequence RNAs (sisRNAs) using total RNA-Seq data from bladder cancer (BC; n  = 457, UROMOL cohort), healthy tissue ( n  = 46), and fractionated cell lines ( n = 5)...
September 2023: NAR cancer
https://read.qxmd.com/read/37507019/activation-of-human-rna-lariat-debranching-enzyme-dbr1-by-binding-protein-ttdn1-occurs-though-an-intrinsically-disordered-c-terminal-domain
#25
JOURNAL ARTICLE
Nathaniel E Clark, Adam Katolik, Pascal Gallant, Anastasia Welch, Eileen Murphy, Luke Buerer, Christoph Schorl, Nandita Naik, Mandar T Naik, Stephen P Holloway, Kristin Cano, Susan T Weintraub, Katherine M Howard, P John Hart, Gerwald Jogl, Masad Damha, William G Fairbrother
In eukaryotic cells, the introns are excised from pre-mRNA by the spliceosome. These introns typically have a lariat configuration due to the 2'-5' phosphodiester bond between an internal branched residue and the 5' terminus of the RNA. The only enzyme known to selectively hydrolyze the 2'-5' linkage of these lariats is the RNA lariat debranching enzyme Dbr1. In humans, Dbr1 has been shown to be involved in processes such as class-switch recombination of immunoglobulin genes, and its dysfunction has been implicated in viral encephalitis, HIV, ALS, and cancer...
July 26, 2023: Journal of Biological Chemistry
https://read.qxmd.com/read/37497541/leader-peptide-removal-in-lasso-peptide-biosynthesis-based-on-penultimate-isoleucine-residue
#26
JOURNAL ARTICLE
Yuwei Duan, Weijing Niu, Linlin Pang, Da-Shuai Mu, Zong-Jun Du, Youming Zhang, Xiaoying Bian, Guannan Zhong
Lasso peptides are ribosomally synthesized peptides that undergo post-translational modifications including leader peptide removal by B (or the segregated B1 and B2) proteins and core peptide macrolactamization by C proteins to form a unique lariat topology. A conserved threonine residue at the penultimate position of leader peptide is hitherto found in lasso peptide precursors and shown to be a critical recognition element for effective enzymatic processing. We identified a lasso peptide biosynthetic gene cluster ( bsf ) from Bradymonas sediminis FA350, a Gram-negative and facultatively prey-dependent bacterium that belongs to a novel bacterial order Bradymonadales in the class Deltaproteobacteria ...
2023: Frontiers in Microbiology
https://read.qxmd.com/read/37493499/direct-current-cardioversion-practices-following-percutaneous-left-atrial-appendage-closure
#27
JOURNAL ARTICLE
Sapan Bhuta, Adnan Shaaban, Nkongho C Binda, James Antaki, Ralph S Augostini, Steven J Kalbfleisch, Salvatore J Savona, Toshimasa Okabe, Mahmoud Houmsse, Muhammad R Afzal, Emile G Daoud, John D Hummel
INTRODUCTION: Among patients with non-valvular atrial fibrillation (AF) and percutaneous left atrial appendage closure (LAAC) undergoing direct current cardioversion (DCCV), the need for and use of LAA imaging and oral anticoagulation (OAC) is unclear. OBJECTIVE: The purpose of this study is to evaluate the real-world use of transesophageal echocardiography (TEE) or cardiac computed tomography angiography (CCTA) before DCCV and use of OAC pre- and post-DCCV in patients with AF status post percutaneous LAAC...
July 26, 2023: Journal of Cardiovascular Electrophysiology
https://read.qxmd.com/read/37441768/structure-and-function-of-spliceosomal-deah-box-atpases
#28
REVIEW
Marieke Enders, Piotr Neumann, Achim Dickmanns, Ralf Ficner
Splicing of precursor mRNAs is a hallmark of eukaryotic cells, performed by a huge macromolecular machine, the spliceosome. Four DEAH-box ATPases are essential components of the spliceosome, which play an important role in the spliceosome activation, the splicing reaction, the release of the spliced mRNA and intron lariat, and the disassembly of the spliceosome. An integrative approach comprising X-ray crystallography, single particle cryo electron microscopy, single molecule FRET, and molecular dynamics simulations provided deep insights into the structure, dynamics and function of the spliceosomal DEAH-box ATPases...
July 17, 2023: Biological Chemistry
https://read.qxmd.com/read/37398028/the-debranching-enzyme-dbr1-regulates-lariat-turnover-and-intron-splicing
#29
Luke Buerer, Nathaniel Clark, Anastasia Welch, Chaorui Duan, Allison Taggart, Brittany Townley, Jing Wang, Rachel Soemedi, Stephen Rong, Chien-Ling Lin, Yi Zeng, Adam Katolik, Jonathan Staley, Masad Damha, Nima Mosammaparast, William Fairbrother
The majority of genic transcription is intronic. Introns are removed by splicing as branched lariat RNAs which require rapid recycling. The branch site is recognized during splicing catalysis and later debranched by Dbr1 in the rate-limiting step of lariat turnover. Through generation of the first viable DBR1 knockout cell line, we find the predominantly nuclear Dbr1 enzyme to encode the sole debranching activity in human cells. Dbr1 preferentially debranches substrates that contain canonical U2 binding motifs, suggesting that branchsites discovered through sequencing do not necessarily represent those favored by the spliceosome...
June 13, 2023: Research Square
https://read.qxmd.com/read/37380170/let-s-talk-about-u-u-seizing-a-valuable-opportunity-to-better-support-adolescents-living-with-hiv
#30
JOURNAL ARTICLE
Sarah Bernays, Joni Lariat, Wole Ameyan, Nicola Willis
The clinical knowledge that people living with HIV who maintain an undetectable viral load and therefore cannot transmit HIV sexually, known as Undetectable equals Untransmittable (U=U), has reached a critical mass of adults, but it is relatively silenced within adolescent HIV care and support. We argue that understanding the full range of opportunities enabled by viral suppression, including the elimination of transmission risk, could transform adolescents' understanding of living with HIV, incentivise optimal treatment engagement and support and sustain their positive mental health...
June 29, 2023: Sexual Health
https://read.qxmd.com/read/37371033/gpcr-binding-and-jnk3-activation-by-arrestin-3-have-different-structural-requirements
#31
JOURNAL ARTICLE
Chen Zheng, Liana D Weinstein, Kevin K Nguyen, Abhijeet Grewal, Eugenia V Gurevich, Vsevolod V Gurevich
Arrestins bind active phosphorylated G protein-coupled receptors (GPCRs). Among the four mammalian subtypes, only arrestin-3 facilitates the activation of JNK3 in cells. In available structures, Lys-295 in the lariat loop of arrestin-3 and its homologue Lys-294 in arrestin-2 directly interact with the activator-attached phosphates. We compared the roles of arrestin-3 conformational equilibrium and Lys-295 in GPCR binding and JNK3 activation. Several mutants with enhanced ability to bind GPCRs showed much lower activity towards JNK3, whereas a mutant that does not bind GPCRs was more active...
June 6, 2023: Cells
https://read.qxmd.com/read/37369199/a-functional-link-between-lariat-debranching-enzyme-and-the-intron-binding-complex-is-defective-in-non-photosensitive-trichothiodystrophy
#32
JOURNAL ARTICLE
Brittany A Townley, Luke Buerer, Ning Tsao, Albino Bacolla, Fadhel Mansoori, Timur Rusanov, Nathanial Clark, Negar Goodarzi, Nicolas Schmidt, Sridhar Nonavinkere Srivatsan, Hua Sun, Reilly A Sample, Joshua R Brickner, Drew McDonald, Miaw-Sheue Tsai, Matthew J Walter, David F Wozniak, Alex S Holehouse, Vladimir Pena, John A Tainer, William G Fairbrother, Nima Mosammaparast
The pre-mRNA life cycle requires intron processing; yet, how intron-processing defects influence splicing and gene expression is unclear. Here, we find that TTDN1/MPLKIP, which is encoded by a gene implicated in non-photosensitive trichothiodystrophy (NP-TTD), functionally links intron lariat processing to spliceosomal function. The conserved TTDN1 C-terminal region directly binds lariat debranching enzyme DBR1, whereas its N-terminal intrinsically disordered region (IDR) binds the intron-binding complex (IBC)...
June 20, 2023: Molecular Cell
https://read.qxmd.com/read/37292947/the-p97-vcp-adapter-ubxd1-drives-aaa-remodeling-and-ring-opening-through-multi-domain-tethered-interactions
#33
Julian R Braxton, Chad R Altobelli, Maxwell R Tucker, Eric Tse, Aye C Thwin, Michelle R Arkin, Daniel R Southworth
p97/VCP is an essential cytosolic AAA+ ATPase hexamer that extracts and unfolds substrate polypeptides during protein homeostasis and degradation. Distinct sets of p97 adapters guide cellular functions but their roles in direct control of the hexamer are unclear. The UBXD1 adapter localizes with p97 in critical mitochondria and lysosome clearance pathways and contains multiple p97-interacting domains. We identify UBXD1 as a potent p97 ATPase inhibitor and report structures of intact p97:UBXD1 complexes that reveal extensive UBXD1 contacts across p97 and an asymmetric remodeling of the hexamer...
May 15, 2023: bioRxiv
https://read.qxmd.com/read/37277335/the-ubx-domain-in-ubxd1-organizes-ubiquitin-binding-at-the-c-terminus-of-the-vcp-p97-aaa-atpase
#34
JOURNAL ARTICLE
Mike Blueggel, Alexander Kroening, Matthias Kracht, Johannes van den Boom, Matthias Dabisch, Anna Goehring, Farnusch Kaschani, Markus Kaiser, Peter Bayer, Hemmo Meyer, Christine Beuck
The AAA+ ATPase p97/VCP together with different sets of substrate-delivery adapters and accessory cofactor proteins unfolds ubiquitinated substrates to facilitate degradation by the proteasome. The UBXD1 cofactor is connected to p97-associated multisystem proteinopathy but its biochemical function and structural organization on p97 has remained largely elusive. Using a combination of crosslinking mass spectrometry and biochemical assays, we identify an extended UBX (eUBX) module in UBXD1 related to a lariat in another cofactor, ASPL...
June 5, 2023: Nature Communications
https://read.qxmd.com/read/37205393/gpcr-binding-and-jnk3-activation-by-arrestin-3-have-different-structural-requirements
#35
Chen Zheng, Liana D Weinstein, Kevin K Nguyen, Abhijeet Grewal, Eugenia V Gurevich, Vsevolod V Gurevich
Arrestins bind active phosphorylated G protein-coupled receptors (GPCRs). Among the four mammalian subtypes, only arrestin-3 facilitates the activation of JNK3 in cells. In available structures, Lys-295 in the lariat loop of arrestin-3 and its homologue Lys-294 in arrestin-2 directly interact with the activator-attached phosphates. We compared the role of arrestin-3 conformational equilibrium and of Lys-295 in GPCR binding and JNK3 activation. Several mutants with enhanced ability to bind GPCRs showed much lower activity towards JNK3, whereas a mutant that does not bind GPCRs was more active...
May 1, 2023: bioRxiv
https://read.qxmd.com/read/37137707/recursive-splicing-discovery-using-lariats-in-total-rna-sequencing
#36
JOURNAL ARTICLE
Emma R Hoppe, Dylan B Udy, Robert K Bradley
Recursive splicing is a non-canonical splicing mechanism in which an intron is removed in segments via multiple splicing reactions. Relatively few recursive splice sites have been identified with high confidence in human introns, and more comprehensive analyses are needed to better characterize where recursive splicing happens and whether or not it has a regulatory function. In this study, we use an unbiased approach using intron lariats to search for recursive splice sites in constitutive introns and alternative exons in the human transcriptome...
July 2023: Life Science Alliance
https://read.qxmd.com/read/37100409/lariat-preparation-using-a-snare-catheter-for-removal-of-a-pancreaticogastric-stent-in-a-rendezvous-stent-exchange
#37
JOURNAL ARTICLE
Yoshihide Kanno, Haruka Okano, Fumisato Kozakai, Shinsuke Koshita, Takahisa Ogawa, Toshitaka Sakai, Kei Ito
No abstract text is available yet for this article.
December 2023: Endoscopy
https://read.qxmd.com/read/37076232/the-strengths-and-weaknesses-of-left-atrial-appendage-ligation-or-exclusion-lariat-atriaclip-surgical-suture
#38
REVIEW
Randall J Lee, Thorsten Hanke
Left atrial appendage (LAA) epicardial exclusion has been associated with addressing 2 potential deleterious consequences attributed to the LAA, namely, thrombus formation and an arrhythmogenic contributor in advanced forms of atrial fibrillation. With more than 60 years of history, the surgical exclusion of the LAA has been firmly established. Numerous approaches have been used for surgical LAA exclusion including surgical resections, suture ligation, cutting and non-cutting staples, and surgical clips. Additionally, a percutaneous epicardial LAA ligation approach has been developed...
June 2023: Cardiac Electrophysiology Clinics
https://read.qxmd.com/read/36974901/absence-of-sickle-triggers-programmed-cell-death-by-disturbing-alternative-splicing-and-decay-of-mrnas
#39
JOURNAL ARTICLE
Chengyun Wu, Weibo Zhen, Wang Xingsong, Yan Li, Wei Wang, Zhubing Hu
Programmed cell death (PCD) plays fundamental roles in plant development and responses to environmental stresses. Here, we report a protein, SICKLE (SIC), that represses PCD. In Arabidopsis (Arabidopsis thaliana), the loss-of-function mutant of SIC, sic-4, hyper-accumulated lariat intronic RNAs (lariRNAs) and exhibited PCD. The gene encoding a RNA debranching enzyme 1 (DBR1), a rate-limiting enzyme for lariRNAs decay, was overexpressed to reduce the level of lariRNAs in the sic-4 mutant, which led to suppression of PCD...
March 28, 2023: Plant Physiology
https://read.qxmd.com/read/36945544/bioinformatics-guided-discovery-of-biaryl-tailored-lasso-peptides
#40
Hamada Saad, Thomas Majer, Keshab Bhattarai, Sarah Lampe, Dinh T Nguyen, Markus Kramer, Jan Straetener, Heike Br Tz-Oesterhelt, Douglas A Mitchell, Harald Gross
Lasso peptides are a class of ribosomally synthesized and post-translationally modified peptides (RiPPs) that feature an isopeptide bond and a distinct lariat fold. A growing number of secondary modifications have been described that further decorate lasso peptide scaffolds. Using genome mining, we have discovered a pair of lasso peptide biosynthetic gene clusters (BGCs) that include cytochrome P450 genes. Here, we report the structural characterization of two unique examples of (C-N) biaryl-containing lasso peptides...
March 6, 2023: bioRxiv
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