1.Eukaryotic DNAJ/K Database: A Comprehensive Phylogenomic Analysis Platform for the DNAJ/K Family.
Kyeongchae CHEONG ; Jaehyuk CHOI ; Jaeyoung CHOI ; Jongsun PARK ; Suwang JANG ; Yong Hwan LEE
Genomics & Informatics 2013;11(1):52-54
Proteins in DNAJ/K families are ubiquitous, from prokaryotes to eukaryotes, and function as molecular chaperones. For systematic phylogenomics of the DNAJ/K families, we developed the Eukaryotic DNAJ/K Database (EDD). A total of 12,908 DNAJs and 4,886 DNAKs were identified from 339 eukaryotic genomes in the EDD. Kingdom-wide comparison of DNAJ/K families provides new insights on the evolutionary relationship within these families. Empowered by 'class', 'cluster', and 'taxonomy' browsers and the 'favorite' function, the EDD provides a versatile platform for comparative genomic analyses of DNAJ/K families.
Eukaryota
;
Genome
;
HSP40 Heat-Shock Proteins
;
HSP70 Heat-Shock Proteins
;
Humans
;
Molecular Chaperones
;
Proteins
2.Differential expression and implication of m6A methylation in mice with experimental myocardial infarction.
Shu Chen ZHANG ; Xiao Ya ZHAO ; Li Li CHEN ; Xiang ZHOU
Chinese Journal of Cardiology 2023;51(11):1166-1174
Objective: To define differentially expressed N6-adenylate methylation (m6A) genes in the myocardial tissue of mice with myocardial infarction (MI) and explore its potential impact on the pathological process of MI. Methods: The random number table method was used to divide the eighteen SPF C57BL/6J male mice aged from 8 to 10 weeks into MI group (MI group, n=9) and control group (control group, n=9). Modified m6A genes from the myocardial tissue were detected via methylated RNA immunoprecipitation with the next generation sequencing (MeRIP-seq). We explored methylation modified characteristics, verified mRNA expression and m6A modified level by bioinformatics analysis, qPCR and MeRIP-qPCR. Results: The Heatmap revealed that 901 differentially modified m6A genes between MI and control group, of which 537 genes were upregulated, and 364 genes were downregulated. The principal component analysis affirmed that two groups could be distinguished significantly in terms of m6A gene modification. The characteristic sequence of m6A modification was GGACU and mainly concentrated in the coding sequence. According to the conjoint analysis with RNA-seq and MeRIP-seq, 119 genes expressed simultaneous m6A modification difference and mRNA expression difference. The Venn diagram exhibited the positive and negative correlation between m6A modification and mRNA expression. Besides, the GO enrichment analysis indicated that the genes with m6A differential modification in MI group were mainly involved in heart development and other processes. qPCR verified that Gbp6 was up-regulated, while Dnaja1 and Dnajb1 were down-regulated. MeRIP-qPCR revealed that the m6A modification level of Hspa1b was downregulated. Conclusion: Myocardial infarction induces differential modification of m6A in the mice model. In addition, the genes with m6A modification may be affected by methylation related enzymes, thus participating the pathogenesis of MI by regulating apoptosis and inflammation.
Male
;
Animals
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Mice
;
Mice, Inbred C57BL
;
Methylation
;
Myocardial Infarction/genetics*
;
Myocardium
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RNA, Messenger/genetics*
;
HSP40 Heat-Shock Proteins
3.Differential expression and implication of m6A methylation in mice with experimental myocardial infarction.
Shu Chen ZHANG ; Xiao Ya ZHAO ; Li Li CHEN ; Xiang ZHOU
Chinese Journal of Cardiology 2023;51(11):1166-1174
Objective: To define differentially expressed N6-adenylate methylation (m6A) genes in the myocardial tissue of mice with myocardial infarction (MI) and explore its potential impact on the pathological process of MI. Methods: The random number table method was used to divide the eighteen SPF C57BL/6J male mice aged from 8 to 10 weeks into MI group (MI group, n=9) and control group (control group, n=9). Modified m6A genes from the myocardial tissue were detected via methylated RNA immunoprecipitation with the next generation sequencing (MeRIP-seq). We explored methylation modified characteristics, verified mRNA expression and m6A modified level by bioinformatics analysis, qPCR and MeRIP-qPCR. Results: The Heatmap revealed that 901 differentially modified m6A genes between MI and control group, of which 537 genes were upregulated, and 364 genes were downregulated. The principal component analysis affirmed that two groups could be distinguished significantly in terms of m6A gene modification. The characteristic sequence of m6A modification was GGACU and mainly concentrated in the coding sequence. According to the conjoint analysis with RNA-seq and MeRIP-seq, 119 genes expressed simultaneous m6A modification difference and mRNA expression difference. The Venn diagram exhibited the positive and negative correlation between m6A modification and mRNA expression. Besides, the GO enrichment analysis indicated that the genes with m6A differential modification in MI group were mainly involved in heart development and other processes. qPCR verified that Gbp6 was up-regulated, while Dnaja1 and Dnajb1 were down-regulated. MeRIP-qPCR revealed that the m6A modification level of Hspa1b was downregulated. Conclusion: Myocardial infarction induces differential modification of m6A in the mice model. In addition, the genes with m6A modification may be affected by methylation related enzymes, thus participating the pathogenesis of MI by regulating apoptosis and inflammation.
Male
;
Animals
;
Mice
;
Mice, Inbred C57BL
;
Methylation
;
Myocardial Infarction/genetics*
;
Myocardium
;
RNA, Messenger/genetics*
;
HSP40 Heat-Shock Proteins
4.Construction of pQE/Dnajb13 recombinant plasmid and the protein expression.
Journal of Southern Medical University 2013;33(12):1757-1760
OBJECTIVETo construct pQE/Dnajb13 recombinant vector and induce the expression of the fusion protein.
METHODSThe open reading frame (ORF) of Dnajb13 gene was amplified from mouse testis cDNA library by PCR. The products were digested by SacI and SalI and subcloned into pQE vector. After identification by DNA sequence analysis, the recombinant plasmids were transformed into competent E.coli M15 cells. The His/Dnajb13 fusion protein was expressed with IPTG induction and purified with Ni(2+) affinity chromatography. Western blotting was used to detect Dnajb13 expression.
RESULTSThe recombinant vector pQE/Dnajb13 was successfully constructed. His/Dnajb13 fusion protein was expressed abundantly at 4 h after IPTG induction, and Western blot analysis demonstrated the presence of Dnajb13 expression in E.coli M15.
CONCLUSIONSWe have successfully constructed pQE/Dnajb13 recombinant vector, which may facilitate further investigation of the role of Dnajb13 in spermatogenesis.
Animals ; Blotting, Western ; Chromatography, Affinity ; Escherichia coli ; Genetic Vectors ; HSP40 Heat-Shock Proteins ; genetics ; Male ; Mice ; Plasmids ; Polymerase Chain Reaction ; Recombinant Proteins
5.Microarray-based analyses of monocytes from Chinese Uygur patients with Parkinson's disease and cognitive impairment.
Qin LUO ; Huan XIA ; Xinling YANG
Chinese Medical Journal 2014;127(12):2386-2388
Aged
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Cognition Disorders
;
genetics
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F-Box Proteins
;
genetics
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HSP40 Heat-Shock Proteins
;
genetics
;
Humans
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Male
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Monocytes
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metabolism
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Parkinson Disease
;
genetics
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alpha-Synuclein
;
genetics
6.Preparation of the anti-HLJ1 monoclonal antibodies and establishment of method for detection of the antigen.
Xiang LIN ; Li MA ; Jufang WANG ; Yongfa TAN ; Qian WEN ; Wei LUO ; Jin SU ; Ying LIN ; Xiaoning WANG
Chinese Journal of Biotechnology 2008;24(7):1293-1299
Monoclonal antibodies (McAbs) against human liver DnaJ-like protein (HLJ1) was produced by using lymphocyte-hybridoma technique and then one method for the detection of HLJ1 antigen was established. Two hybridoma cell lines which stably secreted monoclonal antibodies against HLJ1 were generated and named for A4C7 and C4C8. Subtypes of the two McAbs were both IgG1, and the antibodies showed high titer and good specificity. Using the prepared monoclonal antibody, human embryonic liver tissues were examined by immunohistochemistry. The results indicated that HLJ1 located in the cytoplasm of the human embryonic liver cell. A double antibodies sandwich ELISA was established by using C4C8 and HRP labeled A4C7. This assay had good specificity, and the lowest detection limit was 7.5 ng/mL and the linear range was 7.5-750 ng/mL. In conclusion, an immunohistochemistry method and a sensitive sandwich ELISA were established for the detection of HLJ1 protein.
Animals
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Antibodies, Monoclonal
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biosynthesis
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Enzyme-Linked Immunosorbent Assay
;
methods
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Female
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HSP40 Heat-Shock Proteins
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blood
;
immunology
;
Humans
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Hybridomas
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secretion
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Immunohistochemistry
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Mice
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Mice, Inbred BALB C
7.Establishment and application of a RT-PCR system for quantifying mRNA of 4 hsp genes in human cells.
Hong-fan LI ; Xing-rong LIU ; Feng-yan HENG ; Ning-hua WU ; Yu-fei SHEN
Acta Academiae Medicinae Sinicae 2002;24(3):321-324
OBJECTIVETo establish a RT-PCR system for detecting mRNA expression level of 4 hsp genes in human cells.
METHODSRT-PCR system was established with gene cloning, gene recombination, in vitro transcription and RT-PCR techniques; The detection of expression level of 4 hsp genes in SW13 cell was carried out with this system.
RESULTSIn SW13 cell, hsp70 and hsp90 alpha were typical heat shock induced genes, while hsp60 and hsp90 beta were efficiently expressed and further induced by heat-shock to various extent.
CONCLUSIONSIn our hands novel RT-PCR system can be used to detect mRNA expression level of 4 human hsp genes.
Chaperonin 60 ; biosynthesis ; genetics ; HSP40 Heat-Shock Proteins ; HSP70 Heat-Shock Proteins ; biosynthesis ; genetics ; HSP90 Heat-Shock Proteins ; biosynthesis ; genetics ; Heat-Shock Proteins ; biosynthesis ; genetics ; Humans ; Leukemia, T-Cell ; metabolism ; pathology ; RNA, Messenger ; biosynthesis ; genetics ; Reverse Transcriptase Polymerase Chain Reaction ; Tumor Cells, Cultured
8.Interaction of Hsp40 with influenza virus M2 protein: implications for PKR signaling pathway.
Zhenhong GUAN ; Di LIU ; Shuofu MI ; Jie ZHANG ; Qinong YE ; Ming WANG ; George F GAO ; Jinghua YAN
Protein & Cell 2010;1(10):944-955
Influenza virus contains three integral membrane proteins: haemagglutinin, neuraminidase, and matrix protein (M1 and M2). Among them, M2 protein functions as an ion channel, important for virus uncoating in endosomes of virus-infected cells and essential for virus replication. In an effort to explore potential new functions of M2 in the virus life cycle, we used yeast two-hybrid system to search for M2-associated cellular proteins. One of the positive clones was identified as human Hsp40/Hdj1, a DnaJ/Hsp40 family protein. Here, we report that both BM2 (M2 of influenza B virus) and A/M2 (M2 of influenza A virus) interacted with Hsp40 in vitro and in vivo. The region of M2-Hsp40 interaction has been mapped to the CTD1 domain of Hsp40. Hsp40 has been reported to be a regulator of PKR signaling pathway by interacting with p58(IPK) that is a cellular inhibitor of PKR. PKR is a crucial component of the host defense response against virus infection. We therefore attempted to understand the relationship among M2, Hsp40 and p58(IPK) by further experimentation. The results demonstrated that both A/M2 and BM2 are able to bind to p58(IPK) in vitro and in vivo and enhance PKR autophosphorylation probably via forming a stable complex with Hsp40 and P58(IPK), and consequently induce cell death. These results suggest that influenza virus M2 protein is involved in p58(IPK) mediated PKR regulation during influenza virus infection, therefore affecting infected-cell life cycle and virus replication.
HSP40 Heat-Shock Proteins
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genetics
;
metabolism
;
Humans
;
Orthomyxoviridae
;
genetics
;
metabolism
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Phosphorylation
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Protein Binding
;
genetics
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Signal Transduction
;
genetics
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Two-Hybrid System Techniques
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Viral Matrix Proteins
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metabolism
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Virus Replication
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genetics
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Virus Uncoating
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eIF-2 Kinase
;
metabolism
9.Proteomic identification and functional characterization of MYH9, Hsc70, and DNAJA1 as novel substrates of HDAC6 deacetylase activity.
Linlin ZHANG ; Shanshan LIU ; Ningning LIU ; Yong ZHANG ; Min LIU ; Dengwen LI ; Edward SETO ; Tso-Pang YAO ; Wenqing SHUI ; Jun ZHOU
Protein & Cell 2015;6(1):42-54
Histone deacetylase 6 (HDAC6), a predominantly cytoplasmic protein deacetylase, participates in a wide range of cellular processes through its deacetylase activity. However, the diverse functions of HDAC6 cannot be fully elucidated with its known substrates. In an attempt to explore the substrate diversity of HDAC6, we performed quantitative proteomic analyses to monitor changes in the abundance of protein lysine acetylation in response to HDAC6 deficiency. We identified 107 proteins with elevated acetylation in the liver of HDAC6 knockout mice. Three cytoplasmic proteins, including myosin heavy chain 9 (MYH9), heat shock cognate protein 70 (Hsc70), and dnaJ homolog subfamily A member 1 (DNAJA1), were verified to interact with HDAC6. The acetylation levels of these proteins were negatively regulated by HDAC6 both in the mouse liver and in cultured cells. Functional studies reveal that HDAC6-mediated deacetylation modulates the actin-binding ability of MYH9 and the interaction between Hsc70 and DNAJA1. These findings consolidate the notion that HDAC6 serves as a critical regulator of protein acetylation with the capability of coordinating various cellular functions.
Acetylation
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Actins
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chemistry
;
metabolism
;
Animals
;
Cell Line
;
Chromatography, High Pressure Liquid
;
HSC70 Heat-Shock Proteins
;
metabolism
;
HSP40 Heat-Shock Proteins
;
metabolism
;
Histone Deacetylase 6
;
Histone Deacetylases
;
metabolism
;
Isotope Labeling
;
Liver
;
metabolism
;
Lysine
;
metabolism
;
Mice
;
Mice, Inbred C57BL
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Mice, Knockout
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Microscopy, Confocal
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Nonmuscle Myosin Type IIA
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metabolism
;
Protein Binding
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Proteomics
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Substrate Specificity
;
Tandem Mass Spectrometry
10.Genetic distribution in Chinese patients with hereditary peripheral neuropathy.
Xiao Xuan LIU ; Xiao Hui DUAN ; Shuo ZHANG ; A Ping SUN ; Ying Shuang ZHANG ; Dong Sheng FAN
Journal of Peking University(Health Sciences) 2022;54(5):874-883
OBJECTIVE:
To analyze the distribution characteristics of hereditary peripheral neuropathy (HPN) pathogenic genes in Chinese Han population, and to explore the potential pathogenesis and treatment prospects of HPN and related diseases.
METHODS:
Six hundred and fifty-six index patients with HPN were enrolled in Peking University Third Hospital and China-Japan Friendship Hospital from January 2007 to May 2022. The PMP22 duplication and deletion mutations were screened and validated by multiplex ligation probe amplification technique. The next-generation sequencing gene panel or whole exome sequencing was used, and the suspected genes were validated by Sanger sequencing.
RESULTS:
Charcot-Marie-Tooth (CMT) accounted for 74.3% (495/666) of the patients with HPN, of whom 69.1% (342/495) were genetically confirmed. The most common genes of CMT were PMP22 duplication, MFN2 and GJB1 mutations, which accounted for 71.3% (244/342) of the patients with genetically confirmed CMT. Hereditary motor neuropathy (HMN) accounted for 16.1% (107/666) of HPN, and 43% (46/107) of HPN was genetically confirmed. The most common genes of HMN were HSPB1, aminoacyl tRNA synthetases and SORD mutations, which accounted for 56.5% (26/46) of the patients with genetically confirmed HMN. Most genes associated with HMN could cause different phenotypes. HMN and CMT shared many genes (e.g. HSPB1, GARS, IGHMBP2). Some genes associated with dHMN-plus shared genes associated with amyotrophic lateral sclerosis (KIF5A, FIG4, DCTN1, SETX, VRK1), hereditary spastic paraplegia (KIF5A, ZFYVE26, BSCL2) and spinal muscular atrophy (MORC2, IGHMBP, DNAJB2), suggesting that HMN was a continuum rather than a distinct entity. Hereditary sensor and autosomal neuropathy (HSAN) accounted for a small proportion of 2.6% (17/666) in HPN. The most common pathogenic gene was SPTLC1 mutation. TTR was the main gene causing hereditary amyloid peripheral neuropathy. The most common types of gene mutations were p.A117S and p.V50M. The symptoms were characterized by late-onset and prominent autonomic nerve involvement.
CONCLUSION
CMT and HMN are the most common diseases of HPN. There is a large overlap between HMN and motor-CMT2 pathogenic genes, and some HMN pathogenic genes overlap with amyotrophic lateral sclerosis, hereditary spastic hemiplegia and spinal muscular atrophy, suggesting that there may be a potential common pathogenic pathway between different diseases.
Amyotrophic Lateral Sclerosis
;
Charcot-Marie-Tooth Disease/genetics*
;
DNA Helicases/genetics*
;
DNA-Binding Proteins/genetics*
;
Flavoproteins
;
HSP40 Heat-Shock Proteins
;
Humans
;
Intracellular Signaling Peptides and Proteins/genetics*
;
Kinesins
;
Ligases/genetics*
;
Molecular Chaperones
;
Multifunctional Enzymes
;
Muscular Atrophy, Spinal/genetics*
;
Mutation
;
Phosphoric Monoester Hydrolases
;
Protein Serine-Threonine Kinases
;
RNA Helicases/genetics*
;
RNA, Transfer
;
Transcription Factors/genetics*