Myocardial infarction biomarker miR-1283
Technical field
The present invention relates to medical diagnosis on disease therapy field, myocardial infarction biomarker miR-1283 is specifically related to, more
Body is related to the application of miR-1283 and its target gene in diagnosis and treatment myocardial infarction.
Background technology
Acute myocardial infarction AMI (AMI) is a kind of angiocardiopathy of most serious, and early stage, accurately diagnosis can ensure to fill again
What note was treated immediately begins to be likely to reduced the death rate.The application of some biomarkers such as cardiac muscle troponin I and diagnosis AMI,
Current diagnosis can be improved, is the new method of acute myocardial infarction AMI.However, miRNA is in the expression of acute myocardial infarction AMI and possible
Effect is that research is less, and conventional research shows that miR-30a is, miR-195 target gene regulation cell related to myocardial hypertrophy
Apoptosis, cell propagation and the cell cycle, they can as diagnosing acute myocardial infarction biomarker potential clinical value, but
It is that these are also far from enough, clinical accurate diagnosis and treatment needs more candidate molecules marks.
Existing research show the neurological susceptibility of miR-1283 precursor and HBV associated hepatocellular carcinomas it is significantly correlated (miRNA-SNPs's
Genetic association is studied and the Integrative Biology of liver cancer is studied, 2011 thesis for the doctorate, Chinese People's Liberation Army's military medicine science
Institute), in addition, miR-1283 low expressions in non-tuberculous mycobacteria the infected's blood plasma, are potentially to differentiate tuberculosis branch
Bacillus infection and the molecular marker of mycobacterium tuberculosis infection (tuberculosis and difference table in non-tuberculous mycobacteria the infected's blood plasma
Up to microRNAs screenings, modern preventive medicine, 2016).The present invention is based on high-flux sequence method, obtains myocardial infarction miRNA
With mRNA expression data, meanwhile, with reference to GEO database hub fleshes infarct correlation miRNA and mRNA data, carry out biological information
Credit analysis checking, picks out miR-1283 from the miRNA and mRNA of candidate and its target gene carries out molecular biology checking, knot
Fruit display, miR-1283 and its target gene and myocardial infarction are closely related.Clinical diagnosis and prevention inspection available for myocardial infarction
Survey, be that clinically the research and development of dependent diagnostic reagent lay the foundation.
The content of the invention
Detect application of the miR-1283 preparation in diagnosing myocardial infarction reagent is prepared.
The sequence of the miR-1283 is shown in sequence table SEQ ID NO 1.
Further, diagnosing myocardial infarction reagent include based on high-flux sequence method and/or based on quantifying PCR method and/
Or based on miR-1283 in probing procedure detection sample.
It is preferred to use northern hybridizing methods, miRNA chip of expression spectrum, ribozyme protection analytical technology, RAKE methods, original position
MiR-1283 transcription in hybridization, bead-based flow-cytometry detection sample.
Described sample is peripheral blood.
It is preferred that, specific amplification miR-1283 primer is included based on quantifying PCR method, further preferably, specificity
The primer sequence for expanding miR-1283 is SEQ ID NO 2;Nucleotide sequence with miR-1283 is included based on probing procedure
The probe of hybridization.
It is an object of the invention to provide application of the miR-1283 target gene in diagnosing myocardial infarction preparation is prepared.
The target gene be DIANA-MICROT, MICRORNA.ORG, MIRDB, RNA22-HAS, TARGETMINER,
MiR-1283 target genes disclosed in TARGETSCAN-VERT databases.
It is preferred that, the target gene is HDAC4, PHC2, THOC5, IL17RA.
Further, diagnosing myocardial infarction reagent include based on high-flux sequence method and/or based on quantifying PCR method and/
Or the transcription of sample miR-1283 target genes is detected or based in immunologic detection method detection sample based on probing procedure
The expression of miR-1283 target genes.
It is preferred to use northern hybridizing methods, miRNA chip of expression spectrum, ribozyme protection analytical technology, RAKE methods, original position
The transcription of miR-1283 target genes in hybridization, bead-based flow-cytometry detection sample;Using ELISA and/or collaurum
The expression of miR-1283 target genes in ELISA test strip sample.
Exist it is an object of the invention to provide the active reagent of up-regulation miR-1283 transcription and/or promotion miR-1283
Prepare the application prevented and treated in myocardial infarction preparation.
It is preferred that, using the microRNA gain-of-functions technology based on RNA and/or gene specific miR Mimics skills
Art up-regulation miR-1283 transcription and/or the activity for promoting miR-1283.It is preferred that artificial synthesized short hairpin RNA or by regulation and control open
Mover raises miR-1283.
It is an object of the invention to provide the inhibitor of miR-1283 target gene in preparation prevents and treats myocardial infarction preparation
Application.
It is an object of the invention to provide a kind of myocardial infarction diagnosis reagent, myocardial infarction diagnosis reagent can detect cardiac muscle
MiR-1283 transcription or immunologic detection method detect the target gene that miR-1283 regulates and controls in myocardial infarction sample in infarct sample
Expression.
Further, myocardial infarction diagnosis reagent include detection miRNA regulation and control target gene HDAC4, PHC2, THOC5,
The specific primer of IL17RA expression.
Myocardial infarction treatment medicine or examination are being prepared it is an object of the invention to provide the above-mentioned preparation for preventing and treating myocardial infarction
Application in agent.
Definition:
The method of detection miRNA expression is mainly included based on high throughput sequencing technologies, based on nucleotides at this stage
Hybridization and the miRNA detection methods of PCR-based.MiRNA detection methods based on probe hybridization technique are a kind of direct Detection Methods,
Sample rna need not in advance be expanded, including northern hybridizing methods, miRNA chip of expression spectrum, ribozyme protection analysis skill
The technologies such as art, RAKE methods, in situ hybridization, bead-based flow-cytometry.
(1) Northern hybridizes
Also known as Northern blot is most classical detection eucaryote RNA sizes, estimates the experimental method of its abundance.Base
Present principles are as follows:MiRNA samples are fixed on carrier (such as silicon chip, microballoon or film) first, then it is miscellaneous with the probe of process mark
Hand over, signal detection is carried out after washing unnecessary hybridization probe;Can also the first fixed and target miRNA sequence complementation on carrier
DNA probe, then with the sample miRNA hybridization by mark, then carries out signal detection.The method of signal mark includes isotope
Mark, fluorescence labeling and nano gold mark etc..
(2) miRNA chip of expression spectrum
Principle is equally that the target molecule on solid support is detected using label probe.Pass through miRNA in design chips
Gene and internalcontrol sequence, can Accurate Analysis go out the expression of corresponding miRNA in sample.Genetic chip has high-throughout excellent
Point, can once detect whole expression of hundreds of genes in same sample.The liquid-phase chip that Luminex companies develop
(Liquid chip) is also known as multifunctional suspending dot matrix (Multi analyte suspension array, MASA), is new
Generation biochip technology.Liquid-phase chip system is made up of many spherulas for main matrix, is fixed with not on every kind of spherula
With probe molecule, in order to distinguish different probes, sphere matrix that each is used for label probe is all unique with one
Color numbers, these spherulas are suspended in a liquid-phase system, liquid-phase chip system is just constituted.The system can be to same
Multiple different moleculars in one trace sample carry out quick qualitative and quantitative analysis simultaneously, and this detection technique is referred to as
FMAP (Flexible multianalyte profiling) technology.Molecule hybridization is carried out in aaerosol solution, detection speed pole
It hurry up.
(3) ribozyme protection analytical technology (RPA)
MiRNA detection can also protect analytical technology using ribozyme, and the probe marked and RNA samples to be measured are mixed
Close, hybridize after thermal denaturation, non-hybridized RNA and the single-chain nucleic acid enzymic digestion of unnecessary probe, purify after heat inactivation nuclease by
The RNA molecule of protection, finally by denaturation PAGE electrophoretic separation probes, colour developing.This new method based on solution hybridization is simple
Quickly, sensitivity is high, but is also only used for analyzing known miRNA.
(4) RAKE methods
RAKE methods (RNA primed array based Klenow emzyme) are the bases in miRNA microarray
The Klenow fragments of DNA polymerase i are utilized on plinth, make miRNA and the method for fixed DNA probe hybridization.RAKE can be sensitive
Specifically detect miRNA, it is adaptable to largely quickly screen all miRNA that oneself knows.Can be in specific cell and tumour
Detect miRNA express spectra situations.Moreover, RAKE methods can also be from the tissue of the FFPE secured by formalin
Isolate miRNA and it is analyzed, be the door that analysis miRNA opens hope from sample is achieved.
(5) in situ hybridization (in situ hybridization)
Hybridization in situ technique can intuitively understand miRNA expression ways, be a kind of easier of observation miRNA spatial and temporal expressions
Method, normal mark mode includes digoxin, biotin, fluorescence labeling etc..In situ hybridization (Locked on the basis of locked nucleic acid
Nucleic Acid (LNA) based in situ hybridization (LNA-ISH)) it is the more probe side of current application
Formula.
(6) bead-based flow-cytometry (bead-based flow cytometry)
It is a kind of liquid-phase chip technology, FCM analysis is organically combined, had concurrently by this method with chip technology
Flux is big, detection speed is fast, sensitivity is high and it is specific good the features such as.
(7) Real-Time Fluorescent Quantitative PCR Technique (Real-time PCR, RT-PCR)
Fluoroscopic examination PCR instrument can draw dynamic changing curve to the cumulative speed of extension increasing sequence during whole PCR.Anti-
Answer the initial concentration of target sequence in mixed system bigger, it is desirable to which the PCR cycle number for obtaining amplified production specific output is (general to use
Specific threshold period Ct is expressed) it is fewer.Because miRNA length is only 22nt, it is such that traditional qRT-PCR is not suitable for amplification
Short fragment.There are several real time quantitative PCR methods for miRNA, such as tailing method, neck ring method now.Neck ring method is a kind of
Preferable miRNA detections qRT-PCR methods:Special loop-stem structure primer is designed first, using miRNA to be measured as template reverse transcription
The chains of cDNA first are synthesized, the cDNA one end is stem Loop primer, and stem loop structure, which is opened, substantially increases cDNA length, then
Real-time quantitative PCR amplification is carried out by template design primer of the cDNA of synthesis.QRT-PCR has specificity height, sensitivity good, fast
A variety of advantages such as fast simple.
(8) PCR sequencing PCR
Most of known miRNA is to be sequenced to find and identify by cDNA clone.The method needs first to build miRNA
CDNA library, then enter performing PCR amplification, amplified production be then cloned on expression vector be sequenced.Takada develops one kind and changed
The amplification PCR cloning PCR (miRNA amplification profiling, mRAP) entered, mRAP methods are first connected at miRNA 3 ' ends
Joint, then with the reverse transcription primer reverse transcription complementary with joint.Because specific reverse transcriptase has end deoxynucleotide
Transferase active, some nucleotides (mainly deoxycytidylic acid) can be connected to 3 ' ends of the cDNA chains that reverse transcription goes out.When 5 '
End connector is the achievable PCR expansions to cDNA with after poly (C) cohesive end annealing of cDNA chains, adding a pair of general primers
Increase.Due to mRAP High sensitivities, the expression quantity of miRNA in a small amount of tissue can be directly detected with clone and sequencing technologies.Label
Sequence PCR cloning PCR is a kind of to have developed detection efficiency on the basis of serial analysis of gene expression (SAGE) technology higher
MiRAGE (miRNA SAGE) PCR cloning PCR, the method sub-series big by generating can detect multiple by single sequencing reaction
MiRNA, hence it is evident that improve detection efficiency.
High-flux sequence (High-throughput sequencing) is also known as sequencing technologies (next of future generation
Generation sequencing) it is the change to tradition sequencing revolution, once to hundreds of thousands to millions of DNA
Molecule carries out sequencing, greatly improves sequencing efficiency.This kind of large scale sequencing technology greatly improves multiple species and lost
The solution reading rate of information is passed, to obtain all miRNA sequence information, decryption miRNA collection of illustrative plates, which is provided, to be ensured.While high flux
The analysis for make it that careful overall picture is carried out to the transcript profile and genome of a species is sequenced, so the depth that is otherwise known as
It is sequenced (deep sequencing).The representative of high-flux sequence platform is 454 sequenator (Roch of Roche Holding Ag (Roche)
GSFLX sequencer), the Solexa genome analysises instrument (Illumina Genome Analyzer) of Illumina companies and
ABI SOLiD sequenators (ABI SOLiD sequencer).
MicroRNA gain-of-functions technology based on RNA be by exogenous supplement miRNAs synthesis precursor substance come
Raise miRNAs level.For example, can be with the artificial synthesized bob folder sample RNA (short consistent with endogenous miRNA sequence
Hairpin RNA, shRNA), promoter is done by polymerase II or III, with virus for carrier transfectional cell, by Dicer enzyme modifications
RISC is loaded into afterwards to play a role, it is lasting equivalent to rise pre-miRNA level, action effect stabilization.
This technique avoids the nonspecific action of miRNA and gene for gene specific miR Mimics technologies.This people
The specific oligonucleotide chain combined with the UTR of target gene 3 ' complementations of work synthesis, can be played with being adjusted after the transcription of miRNA identicals
Section is acted on.
The major way of miRNA regulation and control has two kinds:A kind of is the not fully complementary pairings of 3 ' UTR with target gene mRNA, resistance
The translation of disconnected target gene, so that regulatory gene is expressed;It is another be it is similar with siRNA, when miRNA and mRNA complete complementaries are matched
When, Ago2 albumen directly results in its degraded by cutting mRNA, realizes gene silencing.In a word, miRNA is presently believed to which kind of side
Formula is acted on target gene and miRNA is relevant with the pairing degree of target gene.When miRNA matches incomplete with target gene,
MiRNA is just played a role with the expression for suppressing target gene;When miRNA matches complete with target gene section sequence, it is possible to
Target gene is caused to be broken in complementary region and cause gene silencing.
Brief description of the drawings
Fig. 1 is the ROC curve figure of miR-1283 diagnosing myocardial infarctions
Fig. 2 is miR-1283 relative expression's situation maps
Fig. 3 is HDAC4, PHC2, THOC5, IL17RA gene relative expression's situation map
Embodiment
With reference to specific embodiment, the present invention is expanded on further, is only used for explaining the present invention, and it is not intended that to this
The limitation of invention.It will be understood by those skilled in the art that:Can in the case where not departing from the principle and objective of the present invention
So that these embodiments are carried out with a variety of change, modification, replacement and modification, the scope of the present invention is limited by claim and its equivalent
It is fixed.The experimental method of unreceipted actual conditions in the following example, generally according to normal condition or according to the bar proposed by manufacturer
Part examinations.
The collection of the sample of embodiment 1 and Total RNAs extraction
Hospital in March, 2015 is collected each 6 to the myocardial infarction patient of in September, 2016 peripheral bloods and normal healthy controls peripheral blood.
Diagnosis of Acute Myocardial Infarction standard:According to third time in 2012《Myocardial infarction whole world unified definition》The diagnostic criteria system of recommendation
It is fixed.Detect myocardial necrosis marker (mainly troponin) level to rise and/or decline, at least 1 time more than reference value
99%th percentile of the upper limit, and at least with the symptom of a following ischemic.
1) symptom of myocardial ischemia;
2) the ischemic ECG of kainogenesis changes;
3) there are pathologic Q ripples in electrocardiogram;
4) radiological evidence shows new myocardial activity and lost or new regional wall motion abnormality;
5) coronarography or postmortem find there is fresh thrombus in coronary artery.
Blood rna extraction standard:RNA purity:OD260/280≤1.8,28S/18S≤1;RNA integralities:RIN Zhi≤
7.0.RNA integrality detection methods:(agarose coagulates for Agilent 2100 (RNA 6000Nano kit), agarose gel electrophoresis
Gum concentration:1% agarose gel;Voltage:5V/cm;Time:20min).
Embodiment 2 is sequenced, data analysis and electronically validating
Sequencing:MiRNA and mRNA is carried out with llumina Hiseq2500/Miseq second generations high throughput sequencing technologies
Sequencing, by go joint, go low quality, the process such as depollute completes the processing of data, obtains final data.Pass through transcript profile number
Progress t-test after background correction is carried out to miRNA and mRNA sequencing initial data according to analysis software and obtains P values, is then utilized
Fisher, which is examined, merges P values, screening differential expression miRNA and mRNA.Using including miRanda, miRDB, miRWalk and
These algorithm forecasted varianceses of Targetscan express miRNA target gene, choose >=4 algorithms and predict the target gene come, and
The miRNA for the differential expression being had verified that in miRWalk database lookups target gene.
It is final selected from the differential expression miRNA and mRNA of candidate to miR-1283 and its target gene HDAC4, PHC2,
THOC5, IL17RA, progress later experiments checking.
The electronically validating of embodiment 3
Electronically validating:3 sets of mRNA data sets are obtained from the screening of GEO (Gene Expression Omnibus) database
(GSE48060, GSE34198 and GSE61145-GPL6884) and 2 sets of miRNA data sets (GSE61741, GSE31568), 3 sets
MRNA data sets (GSE48060, GSE34198 and GSE61145-GPL6884) have gene 13680, we by using
MetaMA bags, which are calculated and merged using merging P value methods, obtains 612 (FDR after effect value<0.05) difference expression gene, wherein on
352 are adjusted, 260 are lowered;The common miRNA numbers 848 of 2 sets of data collection (GSE24371, GSE17498).Use R bags
MetaMA merges the analysis of P values to two sets of miRNA data sets, finds 15 differential expression miRNA (FDR<0.001&&|
Combined.ES|>1).As a result show that electronically validating result is consistent with sequencing result expression trend.
It is to set up Receiver Operating Characteristics for single miRNA molecule or the method for the efficiency evaluation of diagnostic model
(receiver operating characteristic, ROC) curve, passes through (the Area Under of area under calculated curve
Curve) come judge diagnosis ability.Area value under ROC curve is between 1.0 and 0.5, in AUC>In the case of 0.5, AUC
Closer to 1, illustrate that diagnosis effect is better, AUC has relatively low accuracy in 0.5-0.7, AUC is fixed in 0.7-0.9
True property, has high accuracy when AUC is more than 0.9.We will utilize GSE31568 data sets (including 70 control groups and 20
Example case group), and then analyzed, as a result show, the AUC of miR-1283 diagnosing myocardial infarctions is 0.886 (see Fig. 1), display
Its accuracy rate is higher, show miR-1283 can as diagnosing myocardial infarction molecular marker.
The collection of the sample of embodiment 4 and the extraction of total serum IgE
1 sample collection:
36 myocardial infarction patients and 22 normal healthy controls crowd peripheral bloods (acquisition time in January, 2014-2015 year 8
Month).
2 Total RNAs extractions:
The processing for removing Rnase of related experiment article:
1. it will be rinsed before the application of all glasswares with DEPC and invade bubble, 120 DEG C of high pressure 20min, 180 DEG C of high temperature dry 2
More than hour.
2. by plastic ware (such as:EP pipes/pipette tips) need before use to be stayed overnight with 0.1%DEPC water enchroachment (invasion)s bubble, after drain liquid,
120 DEG C of high pressure 20min, baking box is dried standby.
Leucocyte is separated
(1) 2m1 anticoagulation cirumferential bloods are taken (blood sampling time is no more than 3h);
(2) isometric sterile PB S are added to be sufficiently mixed in peripheral blood, cell suspension is formed;
(3) 4m1 lymphocyte separation mediums are added in another centrifuge tube;
(4) draw 4m1 cell suspensions be gently added to along tube wall lymphocyte separation medium surface (note not with lymphocyte
Separating liquid is mixed).Centrifuge 1500rpm 20min;
(5) boundary layer (tunica albuginea) is gently suctioned out with suction pipe to enter in another centrifuge tube.Sterile cold PBS is washed 2 times, is washed for last 1 time
Washing can move into cell suspension in EP pipes, and supernatant is removed in centrifugation, for extracting RNA.
RNA is extracted
(1) sample is taken out in -80 DEG C of refrigerators, is shredded, Trizol is added in EP pipes in 1ml/50-100mg ratio,
Homogenized is carried out, 5-l0min is stored at room temperature;
(2) every milliliter of Trizol adds 0.2m1 chloroforms, acutely shakes 15s, is stored at room temperature 2-3min, 12000 at 4 DEG C
Leave heart 15min;
(3) the careful supernatant water 600ul that makes an appointment that suctions out moves into another centrifuge tube (being careful not to be extracted into albumin layer), adds equivalent
Isopropanol, overturns and mixes, be stored at room temperature 10min;
(4) 4 DEG C of 12000g centrifuge l0min, abandon supernatant, bottom visible white material;
(5) the rotation washing of the cold ethanol of lml 75% is added, isopropanol is cleaned;
(6) 4 DEG C of 12000g centrifuge 5min, remove the 5-l0min that dried in the air after ethanol, translucent, are dissolved with 20u1DEPC water
RNA.3u1RNA samples are taken, the electrophoresis in 1.5% Ago-Gel;Lu1RNA samples in UV spectrophotometer measuring concentration,
RNA samples in 1.8-2.0 are considered as with A260/280 qualified.
The RT-PCR of embodiment 5 detects miR-1283 and HDAC4, PHC2, THOC5, IL17RA expression
1 RT-PCR detects miR-1283 expression
Reverse transcription
The preparation of RT systems:1 μ g total serum IgEs are used as template ribonucleic acid;5×miScript HiSpec Buffer 4μl;10×
Nucleics Mix 2μl;miScript Reverse Transcriptase Mix 2μl;Aqua sterilisa filling-in is to 20 μ l.ABI
After 37 DEG C of insulation 60min make reverse transcription reaction complete in 9700 type PCR instruments, 95 DEG C of 5min terminating reactions.Add 80 μ l
Nuclease-free H2O is diluted to 100 μ l, and to be stored in -20 DEG C of refrigerators standby.
Quantitative fluorescent PCR
The preparation of miRNA RT-PCR systems:
Reaction system:MiRNAs detection of expression sets 3 parallel tube reactions every time, and internal reference is used as using snRNA U6.Expand
Increasing program:95℃10min;40 circulations (95 DEG C of 10s, 60 DEG C of 30s).
2 RT-PCR detection target genes HDAC4, PHC2, THOC5, IL17RA expression
Reverse transcription
UsingIII Reverse Transcriptase (invitrogen, article No. 18080-044) enter
Row cDNA reverse transcriptions.Using Reverse Transcriptase kit, converse record synthesis cDNA is carried out to l μ g total serum IgEs with RT Buffer.RT bodies
The preparation of system:5 × RT Buffer, 5 μ l, 10mmol/l dNTP, 1.25 μ l, 0.1mmol/l DTT 2.5 μ l, 30 μm of mol/
2 μ l, 200U/ μ l MMLV of l OligodT 1.25 μ l, the μ g of template ribonucleic acid 1, add aqua sterilisa to the μ l of total system 25.42 DEG C of incubations
1 hour, 72 DEG C 10 minutes, of short duration centrifugation.CDNA is preserved and is put the standby RNA of -20 DEG C of refrigerators.
Quantitative fluorescent PCR
Sequence HDAC4 (NM_006037.3), PHC2 (NM_001330488.1), the THOC5 provided according to GenBank
(NM_001002877.1), IL17RA (NM_001289905.1) designs primer, send company to be synthesized.
The preparation of mRNA RT-PCR systems:
Component |
Addition |
2×mix |
10μl |
Sense primer 10uM |
0.5μl |
Anti-sense primer 10uM |
0.5μl |
Template |
2μl |
Add sterile purified water |
To 25 μ l |
Reaction system:Use PowerGreen PCR Master Mix (invitrogen, article No. 4367659) enter
Row amplification, interior participation in the election GAPDH, experimental implementation is carried out by product description.Amplification program is:95 DEG C of 10min, (95 DEG C of 15s, 55
DEG C 60s) × 35 circulations.
3 statistical analysis
Real-time quantitative PCR sample amplified production solubility curve is all unimodal, illustrates that amplified production only has one, is specificity
Amplification;Amplification curve flex point understands that amplification curve entirety collimation is good, shows that the amplification efficiency of each reaction tube is close, and the limit is put down
And without raising up now, exponent phase slope is larger, illustrates that amplification efficiency is higher;According to qRT-PCR relative quantification formula meter
Experimental group and the multiple proportion of control group destination gene expression are calculated, compares tables of the miR-1283 in myocardial infarction group and control group
Up to level.As a result show:MiR-1283 is about 0.3 times of control group in the expression quantity of illness group, HDAC4, PHC2, THOC5,
IL17RA is at 2.6 times, 2.3 times, 2.2 times and 2.5 times that the expression quantity of illness group is control group, and result above demonstrates high flux
The result of sequencing data analysis.
The culture and transient transfection of the cardiac muscle cell of embodiment 6
First, material prepares:
People's primary cardiomyocytes (Human Cardiac Myocytes, HCM) are purchased from ScienCell companies of the U.S., culture
In special myocardial cells culture base.
LipofectamineTM2000Transfection Reagent(Invitrogen)。
MiR-1283 sequences issue Synesis Company, ask its chemical synthesis miR-1283mimics, miR-1283inhibitor
And its non specific control.
2nd, experimental method
1 miRNA is transiently transfected
Lipofectamine is pressed in operationTM2000 reagent specifications are carried out.24h is thin by the good HCM of growth conditions before transfection
Born of the same parents are inoculated into 6 orifice plates, and cell count is about 4 × 105/ L, cellar culture to transfect the same day, cell fusion degree be 70-80% when
Tested.100nM miR-1283mimics/miR1283inhibitor are added in 250 μ l opti-MEM culture mediums,
It is soft to mix;It is another to dilute 5 μ l Lipofectamine with 250 μ l opti-MEM culture mediumsTM2000 liposomes, it is soft to mix,
It is incubated at room temperature 5min;Opti-MEM- liposomes and Opti-MEM-miRNAs are mixed, 20min is incubated at room temperature, it is multiple to form transfection
Compound:Then said mixture is added in cell culture medium, gently mixed, complete medium is changed after culture 6h.Wherein, it is non-
Specific mimics Negative Control (mimics NC) and inhibitor Negative Control
(inhibitor NC) sequence is used as control.Cell total rna is extracted after culture 24-48h, and reverse transcription is into cDNA, real-time quantitative PCR
The change that miR-1283 is expressed after detection is transiently transfected.
2 experimental results
Transiently transfected using cationic-liposome method, respectively by miR-1283mimics or miR-
1283inhibitor and corresponding control sequence Negative Control (NC) transfection cardiac muscle cell's strain HCM.Transfect after 48h, take out
Carry cell total rna.Using U6 as internal reference, real-time quantitative PCR detects miR-1283 expression.As a result show:Compared with control group,
After HCM transfections miR-1283mimics, miR-1283 expression increases about 3.8 times;Transfect after miR-1283inhibitor,
Expression have dropped nearly 59%.Result above shows, can by transiently transfecting miR-1283mimics and miR-1283inhibitor
Effectively up-regulation or downward miR-1283 expression, reliable results can carry out subsequent experimental.
Embodiment 6 transfects influences of the miR-1283 to Human Cardiomyocytes HDAC4, PHC2, THOC5, IL17RA gene expression
MiR-1283mimics or miR-1283inhibitor and corresponding control sequence Negative will be transiently transfected
HCM cells after Control (NC) are inoculated into 96 orifice plates, after transfection 48h, extract cell total rna.Using GAPDH as internal reference,
Real-time quantitative PCR detects HDAC4, PHC2, THOC5, IL17RA expression.
As a result show:Compared with control group, after HCM transfections miR-1283mimics, HDAC4, PHC2, THOC5, IL17RA
Expression quantity reduce about 19%, 16%, 13% and 15% respectively, after transfection miR-1283inhibitor, HDAC4, PHC2,
THOC5, IL17RA expression quantity rise about 17%, 13%, 10% and 11% respectively, preliminary proof miR-1283 and HDAC4,
PHC2, THOC5, IL17RA targeting relation.
Although describing the present invention with reference to various preferred embodiments, it will be appreciated by those skilled in the art that can carry out each
Change is planted, and available equivalents substitute base region of its component without departing from the present invention.Come in addition, many changes can be carried out
Particular case or material is set to be suitable for the teachings of the present invention without departing from its base region.
SEQUENCE LISTING
<110>Beijing Yang Shen biology information technologies Co., Ltd
<120>Myocardial infarction biomarker miR-1283
<160> 10
<170> PatentIn version 3.3
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