Transcription factor ISL1 is essential for pacemaker development and function.

scientific article

Transcription factor ISL1 is essential for pacemaker development and function. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1172/JCI68257
P932PMC publication ID4563735
P698PubMed publication ID26193633

P50authorChristopher K GlassQ55458945
Xingqun LiangQ64682783
Paola CattaneoQ43014746
P2093author name stringJie Yan
Yunfu Sun
Sylvia M Evans
Xiaoli Zhang
Ju Chen
Cizhong Jiang
Xinkai Cao
Lei Bu
Peng Geng
Qingquan Zhang
Shaowei Zhuang
Gang Wang
Yihan Chen
Xiaodong Zhao
Tao Zhuang
Alexander C Zambon
Indroneal Banerjee
Nathanael J Spann
Lina Luo
Xiaohui Gong
H S Vincent Chen
P2860cites workTopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusionsQ21999527
Familial sinus bradycardia associated with a mutation in the cardiac pacemaker channelQ24300840
Pacemaker channel dysfunction in a patient with sinus node diseaseQ24301951
Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndromeQ24314959
Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node diseaseQ24318595
Simple combinations of lineage-determining transcription factors prime cis-regulatory elements required for macrophage and B cell identitiesQ24617969
A central role for Islet1 in sensory neuron development linking sensory and spinal gene regulatory programsQ24644187
Epidemiology of sudden cardiac death: clinical and research implicationsQ24650947
Tbx3 controls the sinoatrial node gene program and imposes pacemaker function on the atriaQ24681355
Identification and functional characterization of cardiac pacemaker cells in zebrafishQ27313717
Fast gapped-read alignment with Bowtie 2Q27860699
Isl1 identifies a cardiac progenitor population that proliferates prior to differentiation and contributes a majority of cells to the heartQ28190508
Multipotent embryonic isl1+ progenitor cells lead to cardiac, smooth muscle, and endothelial cell diversificationQ28275356
Molecular pathway for the localized formation of the sinoatrial nodeQ28284039
Targeted mutation reveals essential functions of the homeodomain transcription factor Shox2 in sinoatrial and pacemaking developmentQ28506813
Neuregulin-1 promotes formation of the murine cardiac conduction systemQ28507021
Islet-to-LMO stoichiometries control the function of transcription complexes that specify motor neuron and V2a interneuron identityQ28508769
Embryonic lethality and abnormal cardiac myocytes in mice lacking ryanodine receptor type 2.Q28584945
The hyperpolarization-activated channel HCN4 is required for the generation of pacemaker action potentials in the embryonic heartQ28585488
Lethal arrhythmias in Tbx3-deficient mice reveal extreme dosage sensitivity of cardiac conduction system function and homeostasisQ28586231
An essential role of Bmp4 in the atrioventricular septation of the mouse heartQ28586261
PINCH1 plays an essential role in early murine embryonic development but is dispensable in ventricular cardiomyocytesQ28586847
The ryanodine receptor modulates the spontaneous beating rate of cardiomyocytes during developmentQ28587739
Notch signaling regulates murine atrioventricular conduction and the formation of accessory pathwaysQ28591561
Expression of the hyperpolarization-activated cyclic nucleotide-gated cation channel HCN4 during mouse heart developmentQ28591825
Hydrops fetalis, cardiovascular defects, and embryonic lethality in mice lacking the calcitonin receptor-like receptor geneQ28592688
Formation of the sinus node head and differentiation of sinus node myocardium are independently regulated by Tbx18 and Tbx3Q28594589
Distinct phases of cardiomyocyte differentiation regulate growth of the zebrafish heartQ30487250
Direct conversion of quiescent cardiomyocytes to pacemaker cells by expression of Tbx18.Q30544927
Functional characterization of a trafficking-defective HCN4 mutation, D553N, associated with cardiac arrhythmiaQ33151337
HCN4 dynamically marks the first heart field and conduction system precursorsQ33598169
A coupled SYSTEM of intracellular Ca2+ clocks and surface membrane voltage clocks controls the timekeeping mechanism of the heart's pacemaker.Q33722486
Alternative splicing regulates mouse embryonic stem cell pluripotency and differentiationQ33935135
NCoR repression of LXRs restricts macrophage biosynthesis of insulin-sensitizing omega 3 fatty acidsQ34040157
A novel mutation in the HCN4 gene causes symptomatic sinus bradycardia in Moroccan Jews.Q34128155
cAMP Sensitivity of HCN Pacemaker Channels Determines Basal Heart Rate But Is Not Critical for Autonomic Rate ControlQ34130292
A high-resolution map of the three-dimensional chromatin interactome in human cellsQ34378943
Environment drives selection and function of enhancers controlling tissue-specific macrophage identitiesQ34452301
Localization of pacemaking activity in early embryonic heart monitored using voltage-sensitive dye.Q52293882
Optical Monitoring of Spontaneous Electrical Activity of 8-somite Embryonic Chick HeartQ52303015
Formation of the Venous Pole of the Heart From an Nkx2-5-Negative Precursor Population Requires Tbx18Q56000972
New recessive syndrome of microcephaly, cerebellar hypoplasia, and congenital heart conduction defectQ56770946
Direct Nkx2-5 Transcriptional Repression of Isl1 Controls Cardiomyocyte Subtype IdentityQ63364317
The development of the conduction system in the mouse embryo heartQ71398007
Location of pacemaker in chick embryo heart at the time of initiation of heartbeatQ72203787
Targeted inactivation of the sodium-calcium exchanger (Ncx1) results in the lack of a heartbeat and abnormal myofibrillar organizationQ73853279
Ventricular pacing or dual-chamber pacing for sinus-node dysfunctionQ74294883
Impaired cardiac performance in heterozygous mice with a null mutation in the sarco(endo)plasmic reticulum Ca2+-ATPase isoform 2 (SERCA2) geneQ77801158
Endothelin-1 and Neuregulin-1 convert embryonic cardiomyocytes into cells of the conduction system in the mouseQ81505289
A family of hyperpolarization-activated mammalian cation channelsQ34472604
New insights into pacemaker activity: promoting understanding of sick sinus syndromeQ34617500
Point mutation in the HCN4 cardiac ion channel pore affecting synthesis, trafficking, and functional expression is associated with familial asymptomatic sinus bradycardiaQ34655363
Functional redundancy between human SHOX and mouse Shox2 genes in the regulation of sinoatrial node formation and pacemaking function.Q34947910
RNA sequencing of mouse sinoatrial node reveals an upstream regulatory role for Islet-1 in cardiac pacemaker cellsQ35132359
Isl1 is required for multiple aspects of motor neuron developmentQ35432551
HCN4 provides a 'depolarization reserve' and is not required for heart rate acceleration in miceQ36116647
GO-Elite: a flexible solution for pathway and ontology over-representationQ36145842
Voltage-dependent calcium channels and cardiac pacemaker activity: from ionic currents to genesQ36175118
Stem cells as biological heart pacemakersQ36327036
Endothelin-induced conversion of embryonic heart muscle cells into impulse-conducting Purkinje fibersQ36490548
The integration of spontaneous intracellular Ca2+ cycling and surface membrane ion channel activation entrains normal automaticity in cells of the heart's pacemaker.Q36667321
Induction of Purkinje fiber differentiation by coronary arterializationQ36668306
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disordersQ36968428
Dynamic interactions of an intracellular Ca2+ clock and membrane ion channel clock underlie robust initiation and regulation of cardiac pacemaker functionQ37002243
Biological pacemaker created by minimally invasive somatic reprogramming in pigs with complete heart block.Q37105417
Genesis and regulation of the heart automaticity.Q37216067
Shox2 is essential for the differentiation of cardiac pacemaker cells by repressing Nkx2-5.Q37222054
Development of the pacemaker tissues of the heart.Q37687712
Effect of natural genetic variation on enhancer selection and function.Q38866012
A HCN4+ cardiomyogenic progenitor derived from the first heart field and human pluripotent stem cellsQ39483876
A large permissive regulatory domain exclusively controls Tbx3 expression in the cardiac conduction system.Q39552302
The transcriptional repressor Tbx3 delineates the developing central conduction system of the heart.Q40553027
Islet1 is a direct transcriptional target of the homeodomain transcription factor Shox2 and rescues the Shox2-mediated bradycardiaQ41136701
Phosphorylation and regulation of the Ca(2+)-pumping ATPase in cardiac sarcoplasmic reticulum by calcium/calmodulin-dependent protein kinaseQ41514087
Intracellular Ca2+ oscillations, a potential pacemaking mechanism in early embryonic heart cellsQ41863784
Tamoxifen-inducible gene deletion in the cardiac conduction systemQ42437141
Islet 1 is expressed in distinct cardiovascular lineages, including pacemaker and coronary vascular cellsQ43243916
Replacement of the muscle-specific sarcoplasmic reticulum Ca(2+)-ATPase isoform SERCA2a by the nonmuscle SERCA2b homologue causes mild concentric hypertrophy and impairs contraction-relaxation of the heartQ43778748
The sinus venosus progenitors separate and diversify from the first and second heart fields early in developmentQ44464144
Sinoatrial node dysfunction and early unexpected death of mice with a defect of klotho gene expressionQ44810019
Role of HCN4 channel in preventing ventricular arrhythmiaQ45804174
Whole-genome and whole-exome sequencing of bladder cancer identifies frequent alterations in genes involved in sister chromatid cohesion and segregationQ45823928
Pinch1 is required for normal development of cranial and cardiac neural crest-derived structures.Q45957952
Sarcoplasmic reticulum Ca(2+)-ATPase overexpression by adenovirus mediated gene transfer and in transgenic miceQ46112930
Mesenchymal stem cells as a gene delivery system to create biological pacemaker cells in vitroQ47315174
T-box transcription factor TBX3 reprogrammes mature cardiac myocytes into pacemaker-like cells.Q51803470
Molecular analysis of patterning of conduction tissues in the developing human heart.Q51867176
Notch1b and neuregulin are required for specification of central cardiac conduction tissue.Q52025862
P433issue8
P407language of work or nameEnglishQ1860
P921main subjectRNA sequencingQ2542347
P304page(s)3256-3268
P577publication date2015-07-20
P1433published inJournal of Clinical InvestigationQ3186904
P1476titleTranscription factor ISL1 is essential for pacemaker development and function
P478volume125

Reverse relations

cites work (P2860)
Q89068535Cardiac-specific developmental and epigenetic functions of Jarid2 during embryonic development
Q64238176Collaborative ISL1/GATA3 interaction in controlling neuroblastoma oncogenic pathways overlapping with but distinct from MYCN
Q49923297Comparative developmental biology of the cardiac inflow tract.
Q39347586Concise Review: Criteria for Chamber-Specific Categorization of Human Cardiac Myocytes Derived from Pluripotent Stem Cells
Q92495861Correlations between ISL1 rs1017 polymorphism and congenital heart disease risk: A PRISMA-compliant meta-analysis
Q45262771Development and Function of the Cardiac Conduction System in Health and Disease
Q38987999Development of the cardiac pacemaker
Q36372470Genetic Regulation of Sinoatrial Node Development and Pacemaker Program in the Venous Pole
Q92732166HIF-1α is required for development of the sympathetic nervous system
Q92217593Hand2 Selectively Reorganizes Chromatin Accessibility to Induce Pacemaker-like Transcriptional Reprogramming
Q67471784High-resolution transcriptional dissection of in vivo Atoh1-mediated hair cell conversion in mature cochleae identifies Isl1 as a co-reprogramming factor.
Q37210954ISL1 and JMJD3 synergistically control cardiac differentiation of embryonic stem cells
Q90397440Identification and Functional Characterization of an ISL1 Mutation Predisposing to Dilated Cardiomyopathy
Q93357355Insulin gene enhancer binding protein 1 induces adipose tissue‑derived stem cells to differentiate into pacemaker‑like cells
Q92835974Iran's Contribution to Human Proteomic Research
Q46520695Isl1 mediates mesenchymal expansion in the developing external genitalia via regulation of Bmp4, Fgf10, and Wnt5a.
Q46744561Mammalian γ2 AMPK regulates intrinsic heart rate
Q47841255Mutations in Hnrnpa1 cause congenital heart defects
Q38649331New Approaches to Biological Pacemakers: Links to Sinoatrial Node Development
Q55019102No effect of thymosin beta-4 on the expression of the transcription factor Islet-1 in the adult murine heart.
Q48172096On the Evolution of the Cardiac Pacemaker
Q50420940Prospective Isolation of ISL1+ Cardiac Progenitors from Human ESCs for Myocardial Infarction Therapy.
Q50048221Protein Kinase 2β Is Expressed in Neural Crest-Derived Urinary Pacemaker Cells and Required for Pyeloureteric Contraction
Q46425614Same-Single-Cell Analysis of Pacemaker-Specific Markers in Human Induced Pluripotent Stem Cell-Derived Cardiomyocyte Subtypes Classified by Electrophysiology.
Q97537622Silencing miR-370-3p rescues funny current and sinus node function in heart failure
Q48106167Spatially resolved RNA-sequencing of the embryonic heart identifies a role for Wnt/β-catenin signaling in autonomic control of heart rate.
Q38920721Spatiotemporal regulation of enhancers during cardiogenesis
Q42379949Tbx18 and the generation of a biological pacemaker. Are we there yet?
Q51419661Temporal requirements for ISL1 in sympathetic neuron proliferation, differentiation, and diversification.
Q26770904The formation and function of the cardiac conduction system
Q90213929Transcription Factor prrx1 Promotes Brown Adipose-Derived Stem Cells Differentiation to Sinus Node-Like Cells
Q89014504Transcriptional regulation of the cardiac conduction system
Q38695345Transient Notch Activation Induces Long-Term Gene Expression Changes Leading to Sick Sinus Syndrome in Mice
Q48183264nkx genes establish SHF cardiomyocyte progenitors at the arterial pole and pattern the venous pole through Isl1 repression.

Search more.