RNAi-mediated knock-down of gene mN6A1 reduces cell proliferation and decreases protein translation.

Abstract:

:Methyltransferases play essential roles in modulating important cellular and metabolic processes. A mouse putative N6-DNA methyltransferase gene (GenBank No AY456393) is a novel gene named mN6amt1(mN6A1). To investigate its function in cell fate and protein translation, RNA interference (RNAi)-mediated knock-down method was established. Cell cycle analysis suggests that the cell proliferation decreases after RNAi with mN6A1. The expression plasmid of luciferase was used to detect protein translation, and the results showed that luciferase expression decreased after RNAi with mN6A1, whereas increased after over-expression of mN6A1 or/and eRF1. The binding between mN6A1 and eRF1 was identified by co-immunoprecipitation and pull-down experiments. It might be suggested that mN6A1 participates in protein translation through interaction with eRF1.

journal_name

Mol Biol Rep

authors

Liu Y,Nie D,Huang Y,Lu G

doi

10.1007/s11033-008-9243-2

subject

Has Abstract

pub_date

2009-04-01 00:00:00

pages

767-74

issue

4

eissn

0301-4851

issn

1573-4978

journal_volume

36

pub_type

杂志文章
  • Expression and roles of As-NUPR1 protein from Artemia sinica during embryo development and in response to salinity stress.

    abstract::As-NUPR1, a stress-related protein, plays an important role in post-diapause during embryonic development in the brine shrimp Artemia sinica. In the present study, successful expression of As-NUPR1 from the cDNA sequence isolated from A. sinica was demonstrated using a prokaryotic expression system. The recombinant pr...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-014-3208-4

    authors: Zhang R,Yao F,Cheng C,Chen Y,Lv Y,Li Z,Zhao N,Wang T,Xin W,Zou X,Hou L

    更新日期:2014-05-01 00:00:00

  • Cardioprotective role of FA against isoproterenol induced cardiac toxicity.

    abstract::The present study was designed to investigate the protective effect of ferulic acid (FA) against isoproterenol (ISO)-induced cardiac toxicity in rats. Isoproterenol challenged in a dose of 85 mg/kg body weight (b.w.) subcutaneously for two consecutive days in the experimental group resulted in acute cardiac toxicity a...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-018-4297-2

    authors: Jain PG,Mahajan UB,Shinde SD,Surana SJ

    更新日期:2018-10-01 00:00:00

  • Interactions of interleukin-12A and interleukin-12B polymorphisms on the risk of intracranial aneurysm.

    abstract::Several lines of evidence indicate that inflammatory processes play pivotal role in the development of intracranial aneurysm (IA). Recently, polymorphisms in the interleukin-12 (IL-12) gene were shown to be associated with immune-mediated inflammatory disease. The aim of this study was to investigate the interactions ...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-012-2031-z

    authors: Li LJ,Pan XM,Sima X,Li ZH,Zhang LS,Sun H,Zhu Y,Liang WB,Gao LB,Zhang L

    更新日期:2012-12-01 00:00:00

  • The expression and activation of ERK/MAPK pathway in human esophageal cancer cell line EC9706.

    abstract::While there have been more and more studies concerning mitogen-activated protein kinases (MAPKs) signaling pathways, which control many cellular complex programmes, such as cell proliferation, differentiation, cell death and embryogenesis. However, few studies are carried out about expression and activation of classic...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-010-0178-z

    authors: Zheng ST,Huo Q,Tuerxun A,Ma WJ,Lv GD,Huang CG,Liu Q,Wang X,Lin RY,Sheyhidin I,Lu XM

    更新日期:2011-02-01 00:00:00

  • Isolation of microsatellite loci for the endangered vermetid gastropod Dendropoma lebeche using Illumina MiSeq next generation sequencing technology.

    abstract::Dendropoma petraeum, considered the primary vermetid reef-building species in the Mediterranean, has recently been shown to be a species complex of at least four cryptic species. These species have highly restricted, non-overlapping distributions, causing concern for their conservation status. To better study the gene...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-018-4346-x

    authors: López-Márquez V,García-Jiménez R,Calvo M,Templado J,Machordom A

    更新日期:2018-12-01 00:00:00

  • An association between polymorphism of the heme oxygenase-1 and -2 genes and age-related macular degeneration.

    abstract::Iron may be implicated in the generation of oxidative stress by the catalyzing the Haber-Weiss or Fenton reaction. On the other hand, oxidative stress has been implicated in the pathogenesis of age-related macular degeneration (AMD) and heme oxygenase-1 (HO-1), encoded by the HMOX1 gene and heme oxygenase-2 (HO-2), en...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-011-0955-3

    authors: Synowiec E,Szaflik J,Chmielewska M,Wozniak K,Sklodowska A,Waszczyk M,Dorecka M,Blasiak J,Szaflik JP

    更新日期:2012-03-01 00:00:00

  • A functional polymorphism, rs28493229, in ITPKC and risk of Kawasaki disease: an integrated meta-analysis.

    abstract::Kawasaki disease (KD) is a multi-systemic vasculitis which preferentially affects infants and children. A single nucleotide polymorphism (rs28493229) in the inositol 1,4,5-trisphosphate 3-kinase C (ITPKC) was identified to be associated with the increased risk of KD; however, in more recent studies associations have b...

    journal_title:Molecular biology reports

    pub_type: 杂志文章,meta分析

    doi:10.1007/s11033-012-2022-0

    authors: Lou J,Xu S,Zou L,Zhong R,Zhang T,Sun Y,Lu X,Liu L,Li C,Wang L,Xiong G,Wang W,Gong F,Wu J

    更新日期:2012-12-01 00:00:00

  • Genome-wide analysis of the MATE gene family in potato.

    abstract::The multidrug and toxic compound extrusion (MATE) protein family is a newly discovered family of secondary transporters that extrude metabolic waste and a variety of antibiotics out of the cell using an electrochemical gradient of H+ or Na+ across the membrane. The main function of MATE gene family is to participate i...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-018-4487-y

    authors: Li Y,He H,He LF

    更新日期:2019-02-01 00:00:00

  • Genetic diversity in some grape varieties revealed by SCoT analyses.

    abstract::Start codon targeted (SCoT) polymorphic markers were used to assess genetic relationships among 64 grape varieties. Seventeen informative primers were selected from 36 SCoT primers based on their ability to produce clear and repeatable polymorphic and unambiguous bands among the varieties. A total of 131 bands were pr...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-011-1329-6

    authors: Guo DL,Zhang JY,Liu CH

    更新日期:2012-05-01 00:00:00

  • The nature of the differential inhibition of polyphenylalanine synthesis in extracts from Artemia salina and rabbit reticulocytes by the Phytolacca americana protein.

    abstract::The difference in sensitivity of polyphenylalanine synthesis in extracts from Artemia salina and rabbit reticulocytes to inhibition by the Phytolacca americana protein (PAP) has been found to be linked to the source of the supernatant enzyme fraction and not the ribosomes. In the presence of reticulocyte supernatant e...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/BF00366257

    authors: Suits JP,Irvin JD

    更新日期:1976-04-01 00:00:00

  • Genetic diversity of the fungal pathogen Metarhizium spp., causing epizootics in Chinese burrower bugs in the Jingting Mountains, eastern China.

    abstract::Based on the internal transcribed spacer and inter-simple sequence repeats (ISSR), the phylogenetic relationship and genetic diversity of Metarhizium spp., pathogens found in Chinese burrower bugs, Schiodtella formosana, were analyzed. The results showed that the causative agents of the epizootic green muscardine dise...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-012-2088-8

    authors: Luan F,Zhang S,Wang B,Huang B,Li Z

    更新日期:2013-01-01 00:00:00

  • Isolation of Ty1-copia retrotransposon in myrtle genome and development of S-SAP molecular marker.

    abstract::Long terminal repeat (LTR)-retrotransposons are mobile genetic elements that are ubiquitous in plants and constitute a major portion of their nuclear genomes. LTR- retrotransposons possess unique properties that make them appropriate for investigating relationships between populations, varieties and closely related sp...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-011-1112-8

    authors: Woodrow P,Pontecorvo G,Ciarmiello LF

    更新日期:2012-04-01 00:00:00

  • Gallic and vanillic acid suppress inflammation and promote myelination in an in vitro mouse model of neurodegeneration.

    abstract::Neuroinflammation affects millions of people around the world as a result of injury or stress. Neuroinflammation represents almost all types of neurological diseases such as multiple sclerosis and Alzheimer's disease. Neurodegenerative diseases comprise demyelination and synaptic loss. The inflammatory response is fur...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-018-4557-1

    authors: Siddiqui S,Kamal A,Khan F,Jamali KS,Saify ZS

    更新日期:2019-02-01 00:00:00

  • The polymorphism analysis of CD169 and CD163 related with the risk of porcine reproductive and respiratory syndrome virus (PRRSV) infection.

    abstract::Porcine reproductive and respiratory syndrome virus (PRRSV) could infect porcine alveolar macrophages (PAM), and the CD169 and CD163 are identified as critical receptors on the surface of PAM, but whether the single nucleotide polymorphisms (SNPs) of these genes could influence the infection is remain unclear. In this...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-012-1857-8

    authors: Ren YW,Zhang YY,Affara NA,Sargent CA,Yang LG,Zhao JL,Fang LR,Wu JJ,Fang R,Tong Q,Xiao J,Li JL,Jiang YB,Chen HC,Zhang SJ

    更新日期:2012-11-01 00:00:00

  • Effects of copper toxicity at different pH and temperatures on the in vitro enzyme activity in blood and liver of fish, Prochilodus lineatus.

    abstract::Blood and liver from curimbata (Prochilodus lineatus) acclimated at pH 4.5, 7.0 and 8.0 and at 20 and 30 °C were exposed in vitro to different concentrations of copper (Cu): 98 ± 0.8 μg Cu L-1 at pH 4.5 and 16 ± 0.2 μg Cu L-1 at pH 8.0 at 20 °C; 88 ± 0.8 μg Cu L-1 at pH 4.5 and 14 ± 0.5 μg Cu L-1 at pH 8.0 at 30 °C an...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-019-04944-y

    authors: Dos Santos Carvalho C,Fernandes MN

    更新日期:2019-10-01 00:00:00

  • Expression patterns of As-ClC gene of Artemia sinica in early development and under salinity stress.

    abstract::As-ClC (chloride channels protein from Artemia sinica), a member from the chloride channels protein family, is a α-helical membrane protein predicted to traverse the cell membrane 11 times. It is important for several physiological functions such as cell volume regulation, cell proliferation, growth and differentiatio...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-012-2441-y

    authors: Zhang Q,Hou M,Li Q,Han L,Yuan Z,Tan J,Du B,Zou X,Hou L

    更新日期:2013-05-01 00:00:00

  • Characterization of a novel human CDK5 splicing variant that inhibits Wnt/beta-catenin signaling.

    abstract::The cyclin-dependent kinases (CDKs) are a family of serine/threonine kinases, playing an essential role in regulating cell-cycle progression. In our present work, human CDK5 and a novel CDK5 splicing variant, named as CDK5-SV, were cloned from the cDNA library of human testis. CDK5-SV lacking the exon 7 of CDK5 encode...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-009-9752-7

    authors: Li Q,Liu X,Zhang M,Ye G,Qiao Q,Ling Y,Wu Y,Zhang Y,Yu L

    更新日期:2010-06-01 00:00:00

  • Molecular and biochemical analysis of the beta class carbonic anhydrases in Caenorhabditis elegans.

    abstract::The beta class of the carbonic anhydrase (CA) enzyme family has been found in plants, yeast, bacteria and algae, but not in animals. Also, little is known concerning the CAs of C. elegans. Genes possibly encoding beta-CAs were revealed by in silico analysis of the C. elegans genome. Amino acid sequence and 3D structur...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-009-9857-z

    authors: Fasseas MK,Tsikou D,Flemetakis E,Katinakis P

    更新日期:2010-07-01 00:00:00

  • Characterization and expression pattern of KIFC1-like kinesin gene in the testis of the Macrobrachium nipponense with discussion of its relationship with structure lamellar complex (LCx) and acroframosome (AFS).

    abstract::Spermiogenesis is a developmental process undergoing continuous differentiation to drive a diploid spermatogonium towards a haploid sperm cell. This striking transformation from spermatogonium to spermatozoa is made possible by the stage-specific adaption of cytoskeleton and associated molecular motor proteins. KIFC1 ...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-012-1593-0

    authors: Wang YT,Mao H,Hou CC,Sun X,Wang DH,Zhou H,Yang WX

    更新日期:2012-07-01 00:00:00

  • Staphylococcus aureus mobile genetic elements.

    abstract::Among the bacteria groups, most of them are known to be beneficial to human being whereas only a minority is being recognized as harmful. The pathogenicity of bacteria is due, in part, to their rapid adaptation in the presence of selective pressures exerted by the human host. In addition, through their genomes, bacter...

    journal_title:Molecular biology reports

    pub_type: 杂志文章,评审

    doi:10.1007/s11033-014-3367-3

    authors: Alibayov B,Baba-Moussa L,Sina H,Zdeňková K,Demnerová K

    更新日期:2014-08-01 00:00:00

  • Two mutations in LDLR gene were found in two Chinese families with familial hypercholesterolemia.

    abstract::Familial hypercholesterolemia (FH) (OMIM 143890) is an autosomal dominantly inherited disease mainly caused by mutations of the gene encoding the low density lipoprotein receptor (LDLR) and Apolipoprotein (Apo) B. First the common mutation R3500Q in ApoB gene was determined using PCR/RFLP method. Then the LDLR gene wa...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-008-9416-z

    authors: Cheng X,Ding J,Zheng F,Zhou X,Xiong C

    更新日期:2009-11-01 00:00:00

  • rs2651899 variant is associated with risk for migraine without aura from North Indian population.

    abstract::Recently a GWAS study had identified 38 genomic variants commonly found in humans that influence migraine risk. For further replicate these findings, we selected two SNPs; rs2651899 on chromosome 1p36.32 in PRDM16 gene and rs10166942 on chromosome 2q37.1 close to TRPM8 gene for their associations with migraine in the ...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-019-04593-1

    authors: Kaur S,Ali A,Ahmad U,Pandey AK,Singh B

    更新日期:2019-02-01 00:00:00

  • Genetic structure and diversity analysis of tall fescue populations by EST-SSR and ISSR markers.

    abstract::Tall fescue is a perennial cool-season grass with economic importance especially in temperate regions of the northern hemisphere. This study was done to assess the genetic diversity and population structure of 90 tall fescue populations and cultivars using ISSR and EST-SSR markers in order to categorize valuable popul...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-019-05173-z

    authors: Shahabzadeh Z,Mohammadi R,Darvishzadeh R,Jaffari M

    更新日期:2020-01-01 00:00:00

  • Overexpressed in colorectal carcinoma gene (OCC-1) upregulation and APPL2 gene downregulation in breast cancer specimens.

    abstract::Breast cancer is the most common cancer type and the second cause of cancer death in women. Different mechanisms are contributed to the initiation and progression of the breast cancer. OCC-1 and APPL2 neighboring genes located in 12q.23.3 human chromosome region are related to colorectal cancer. Here, we intended to i...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-018-4336-z

    authors: Ghalaei A,Kay M,Zarrinfam S,Hoseinpour P,Behmanesh M,Soltani BM

    更新日期:2018-12-01 00:00:00

  • Expression of NAT2 in immune system cells and the relation of NAT2 gene polymorphisms in the anti-tuberculosis therapy in Mexican mestizo population.

    abstract::Arylamine N-acetyltransferase 2 (NAT2) metabolizes isoniazid (INH) and Single Nucleotide Polymorphisms (SNP) responsible for its activity has been reported. The aim of this study in the Mexican mestizo population was to evaluate NAT2 expression at the protein level in immune cells, as well as the distribution and freq...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-014-3677-5

    authors: Salazar-González R,Gómez R,Romano-Moreno S,Medellín-Garibay S,Núñez-Ruíz A,Magaña-Aquino M,Milán-Segovia RC,Portales-Pérez DP

    更新日期:2014-12-01 00:00:00

  • Sequence variation in promoter regions of genes for CC chemokine ligands (CCL)19 and 21 in Czech patients with myocardial infarction.

    abstract::Recruitment of inflammatory cells to the arterial wall is an important pathogenic mechanism of atherosclerosis and coronary artery disease (CAD). Functional variability in the genes encoding for chemokines that promote infiltration of atherosclerotic plaques by macrophages and lymphocytes may therefore contribute to t...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-014-3175-9

    authors: Stahelova A,Petrkova J,Petrek M,Mrazek F

    更新日期:2014-05-01 00:00:00

  • A novel missense (A79V) mutation of goat PROP1 gene and its association with production traits.

    abstract::As a paired class homeodomain transcription factor, mutations of PROP1 (Prophet of POU1F1) are responsible for deficiencies of GH, PRL, TSH, LH and FSH. Regarding mutations of GH, PRL, and POU1F1 genes significantly associating with different production traits, PROP1 gene is a novel important candidate gene for detect...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-008-9418-x

    authors: Lan X,Pan C,Zhang L,Zhao M,Zhang C,Lei C,Chen H

    更新日期:2009-11-01 00:00:00

  • Complete mitochondrial DNA sequence and phylogenetic analysis of Zhikong scallop Chlamys farreri (Bivalvia: Pectinidae).

    abstract::The complete mitochondrial genome of Zhikong scallop Chlamys farreri is 21,695 bp in length and contains 12 protein-coding genes (the atp8 gene is absent, as in most bivalves), 2 ribosomal RNA genes, and 22 transfer RNA genes. The heavy strand has an overall A+T content of 58.7%. GC and AT skews for the mt genome of C...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-010-9974-8

    authors: Xu K,Kanno M,Yu H,Li Q,Kijima A

    更新日期:2011-06-01 00:00:00

  • Proteasome inactivation upon aging and on oxidation-effect of HSP 90.

    abstract::Increases of oxidatively modified protein in the cell have been associated with the aging process. Such an accumulation of damaged protein may be the result of increase in the rate of protein oxidation and/or decrease in the rate of degradation of oxidized protein. The multicatalytic proteinase or proteasome is known ...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1023/a:1006852506884

    authors: Conconi M,Friguet B

    更新日期:1997-03-01 00:00:00

  • Association of peroxisome proliferator-activated receptorγ gene Pro12Ala and C161T polymorphisms with cardiovascular risk factors in maintenance hemodialysis patients.

    abstract::The Pro12Ala and C161T polymorphisms in peroxisome proliferator-activated receptor γ (PPARγ) have been shown to be associated with carotid artery atherosclerosis. It remains unclear whether these two polymorphisms are associated with risk factors for cardiovascular disease (CVD) in hemodialysis (HD) patients. Therefor...

    journal_title:Molecular biology reports

    pub_type: 杂志文章

    doi:10.1007/s11033-014-3645-0

    authors: Liu F,Mei X,Zhang Y,Qi H,Wang J,Wang Y,Jiang W,Zhang X,Yan H,Zhuang S

    更新日期:2014-11-01 00:00:00