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68 results about "Insertion sequence" patented technology

Insertion element (also known as an IS, an insertion sequence element, or an IS element) is a short DNA sequence that acts as a simple transposable element. Insertion sequences have two major characteristics: they are small relative to other transposable elements (generally around 700 to 2500 bp in length) and only code for proteins implicated in the transposition activity (they are thus different from other transposons, which also carry accessory genes such as antibiotic resistance genes). These proteins are usually the transposase which catalyses the enzymatic reaction allowing the IS to move, and also one regulatory protein which either stimulates or inhibits the transposition activity. The coding region in an insertion sequence is usually flanked by inverted repeats. For example, the well-known IS911 (1250 bp) is flanked by two 36bp inverted repeat extremities and the coding region has two genes partially overlapping orfA and orfAB, coding the transposase (OrfAB) and a regulatory protein (OrfA). A particular insertion sequence may be named according to the form ISn, where n is a number (e.g. IS1, IS2, IS3, IS10, IS50, IS911, IS26 etc.); this is not the only naming scheme used, however. Although insertion sequences are usually discussed in the context of prokaryotic genomes, certain eukaryotic DNA sequences belonging to the family of Tc1/mariner transposable elements may be considered to be, insertion sequences.

Method for improving nucleic acid sequencing quality by eliminating nucleic acids with deaminated bases from library and method for sequencing in which complexes of primers, polymerases and labelled probes are bound to concatemers

The present disclosure provides methods for reducing sequencing errors comprising one or any combination of: (i) removing deaminated bases in any nucleic acid molecule throughout a library preparation workflow which includes immobilised splints which bind to the library, the use of a compaction oligonucleotide, optionally with an intervening sequence, formation of closed circular nucleic acids, creating gaps using glycosylase and lyase activities at positions with deaminated bases. The library may be sequenced using pairwise sequencing, e.g. with dark sequencing and / or sequencing using a multivalent labelled probe for the formation of an avidity molecule and soluble primer and polymerase. Method for sequencing concatemers in which the concatermers are contacted with polymerases, soluble primers and a multivalent labelled molecule which forms a complex with the polymerase. Detecting polymerase position and nucleobase bound to the polymerase in the complex. These methods generate higher quality base calls during downstream sequencing workflows.
Owner:ELEMENT BIOSCIENCES INC

InDel marker closely linked with sweet-glutinous same-grain character of corn ear and application of InDel marker

The invention discloses an InDel marker closely linked with the sweet-glutinous homograin character of corn ears, a corn B73-V4 genome is used as a reference genome, the marker is a <-> / insertion sequence of 73 bp located at the position of 12126328 bp of a No.9 chromosome, and the nucleotide sequence of the insertion sequence is as shown in SEQ ID NO.1. The InDel marker closely linked with the sweet-glutinous homograin character of the corn ears has the advantages that the InDel marker closely linked with the sweet-glutinous homograin character of the corn ears is obtained; the InDel marker provided by the invention can be used for rapidly screening out a corn material containing a sweet-waxy homograin gene in the early growth stage of corn, and can also be used for molecular marker-assisted breeding of fresh corn. By adopting the InDel marker and the screening method provided by the invention, the screening accuracy is high, and by using the marker and the screening method, the production cost is saved, and the breeding efficiency is improved.
Owner:INST OF SPECIAL ANIMAL & PLANT SCI OF CAAS

Cotton event cD46-2 as well as primer and method for detecting cotton event cD46-2

The invention provides a cotton transformation event cD46-2 as well as a primer pair and a method for detecting the cotton transformation event cD46-2. The cotton plant carrying the cD46-2 transformation event comprises the event, namely the joint of an exogenous insertion DNA sequence and a cotton genome DNA sequence, on a group A chromosome 2. A detection primer can be designed by using an exogenous insertion DNA sequence and a DNA sequence of a junction region on a flanking cotton genome, and is used for specific detection of a cD46-2 event. The detection method aiming at the cD46-2 event can provide a convenient means for tracking the specific gene insertion event for the application of breeding by using the plant event, and the specific gene insertion event can be used as a molecular marker to improve the working efficiency of fiber improvement breeding by using the transformation event.
Owner:BIOCENTURY TRANSGENE CHINA

Indel molecular marker of avena nuda and application

The invention relates to the technical field of crop molecular genetic markers, and discloses an Indel molecular marker of avena nuda and application of the molecular marker, the molecular marker is insertion variation of 551bp located at the 4D chromosome position 451669339-451669889 of a reference genome of an avena nuda variety Sanfensan, and the insertion sequence is as shown in SEQ ID NO. 1. The Indel molecular marker provided by the invention is completely related to the naked oat skin character, can be efficiently used for naked oat germplasm resource identification, variety purity detection and molecular marker-assisted breeding, remarkably improves the screening efficiency of naked oat excellent germplasm, and provides a brand new molecular detection technology for genetic improvement of the naked oat skin character. According to the invention, not only is a rapid and accurate technical standard established for naked oat variety identification, but also important molecular marker resources and application schemes are provided for oat quality improvement and germplasm innovation.
Owner:CHENGDU UNIV +1

An IS26-based drug resistance gene control plasmid, engineering bacteria, bacterial agent and application

The present invention discloses an IS26-based resistance gene control plasmid, engineering bacteria, bacterial agent and application, belonging to the technical field of genetic engineering. The nucleotide sequence of the IS26-based resistance gene control plasmid is shown in SEQ ID NO: 1 or SEQ ID NO: 2. The engineering bacteria and bacterial agent containing the resistance gene control plasmid can be used for the control of resistance genes. By specifically destroying the insertion sequence IS26, the number of resistance genes can be fundamentally reduced and the spread of resistance genes can be blocked, providing a precise solution for the treatment of drug resistance. It has broad-spectrum resistance bacteria control performance and can effectively control gentamicin, tetracycline, chloramphenicol and ampicillin-resistant bacteria in wastewater, with the highest control efficiency reaching 83.76%. The plasmid, engineering bacteria and bacterial agent have low preparation costs, can be used for in-situ treatment of wastewater, have low treatment costs and good effects, and have broad application prospects.
Owner:NANJING UNIV

Construction of fluorescent protein-tagged tubulin and microtubule-binding protein universal bivalent vectors

ActiveCN115896146BSimplify the experimental processShorten the interactive research cycleFermentationVector-based foreign material introductionInsertion sequenceTransgene
The application provides a construction of a fluorescent protein labeled microtubulin and a microtubule binding protein universal bivalent carrier, and the process is as follows: a first stage is to construct a GFP-alpha tubulin carrier, and a second stage is to construct a GFP-alpha tubulin-mCherry universal bivalent co-expression carrier; in the second stage, 35S, mCherry and NOS sequences are inserted into a KpnI enzyme cutting site of a multiple cloning site of the GFP-alpha tubulin carrier constructed in the first stage, and a single nucleic acid enzyme cutting site is inserted into the 5' end and the 3' end of the mCherry sequence, respectively, and the single nucleic acid enzyme cutting site is XbaI, KpnI / Acc65I and AscI sequences, respectively, so as to obtain the universal bivalent carrier. The universal bivalent carrier provided by the application can express two target genes simultaneously, has the fluorescent signals of GFP and mCherry, can quickly and accurately identify a transgenic plant, is convenient for positive seedling screening, can be used for a tobacco transient expression experiment, can shorten an experimental period, and saves time and effort.
Owner:DEZHOU UNIV

InDel molecular marker closely linked with soybean protein content character, detection primer and application

The invention discloses an InDel molecular marker closely linked with soybean protein content characters, a detection primer and application, and belongs to the technical field of molecular biology. The nucleotide sequence of the InDel molecular marker is shown as SEQ ID NO.5, the 96th site to the 106th site of the SEQ ID NO.5 are insertion or deletion variation, and the soybean containing the 96th site to the 106th site insertion sequence of the SEQ ID NO.5 is a variety with high protein content; and the soybean containing the 96th-106th deletion sequence of the SEQ ID NO.5 is a variety with low protein content. According to the invention, 11bp insertion / deletion variation at 377 and 973bp positions of the soybean 14 # chromosome is found, and experiments show that the 11bp insertion / deletion variation has remarkable relevance with the soybean protein content. When the gene is applied to molecular assisted breeding, the protein content expression of a soybean candidate material can be predicted at an early stage.
Owner:JIANGSU ACAD OF AGRI SCI

Glyphosate and glufosinate herbicide resistant corn transformation event LE4 and detection method thereof

The invention relates to an exogenous insertion sequence of a glyphosate and glufosinate-ammonium resistant corn transformation event LE4, a detection method and application. A nucleic acid molecule sequence of the corn LE4 comprises SEQ ID NO.1 or SEQ ID NO.2 or SEQ ID NO.13 or a reverse complementary sequence of the SEQ ID NO.1 or SEQ ID NO.2 or SEQ ID NO.13. The invention further relates to a method for detecting the glyphosate and glufosinate-ammonium resistant corn transformation event LE4. The corn transformation event LE4 has glyphosate and glufosinate herbicide resistance and excellent agronomic traits, and the detection method can accurately and quickly identify whether a biological sample contains DNA molecules of the transgenic corn event LE4 or not.
Owner:SHANDONG ACADEMY OF AGRICULTURAL SCIENCES

Primer and probe combination as well as method and application thereof

The invention discloses a primer and probe combination as well as a method and application thereof. The invention relates to the technical field of molecular biology, in particular to a primer and probe combination for detecting a herbicide tolerance transgenic soybean event DBN9004 through RAA-LFD as well as a method and application of the primer and probe combination. A plurality of RAA primers are designed according to a connection region of an exogenous insertion DNA sequence and a soybean genome, and a pair of primer and probe combination capable of rapidly and effectively detecting the DBN9004 component in the transgenic soybean is screened from the RAA primers. The detection method can be used for rapidly and accurately identifying DBN9004DNA molecules in a sample, and has the characteristics of simplicity and convenience in operation, high speed, good specificity and the like.
Owner:ZHAOFENGHUA BIOTECHNOLOGY (NANJING) CO LTD BEIJING BIOMEDICAL TECH CENT +1

Modified bacterial strains

Described herein is a modified bacterial strain lacking an insertion sequence (IS), wherein the modified bacterial strain (i) includes a specific deletion of an IS present in an unmodified bacterial strain, and (ii) retains non-IS sequences flanking the IS in the unmodified bacterial strain. There is also provided a method for producing said modified bacterial strains, the method comprising: (a) providing a bacterial strain comprising an IS flanked by non-IS sequences; and (b) specifically deleting the IS in the bacterial strain without deleting non-IS sequences flanking the IS.
Owner:INST OF SCI & TECH AUSTRIA

Corn event CSJ4351 and primer and method for detecting same

The invention provides a corn transformation event CSJ4351 as well as a primer pair and a method for detecting the corn transformation event CSJ4351. The maize plant carrying the CSJ4351 transformation event comprises the event on a chromosome 3, namely the junction of an exogenous insertion DNA sequence and a maize genome DNA sequence. A detection primer can be designed by using an exogenous insertion DNA sequence and a DNA sequence of a junction region on a flanking corn genome, and is used for specific detection of a CSJ4351 event. The detection method aiming at the CSJ4351 event can provide a convenient means for tracking the insertion event of the specific gene for breeding by using the plant event, and the insertion event of the specific gene can be used as a molecular marker to improve the working efficiency of insect-resistant and herbicide-resistant breeding by using the transformation event.
Owner:BIOCENTURY TRANSGENE CHINA

Specific marker of intergenic region of recd / mtl5 gene of oplegnathus fasciatus, detection method and application

PendingCN122445820ABase JNucleotide
The present application relates to molecular biology technology, specifically to a specific marker of Oplegnathus punctatus recd / mtl5 intergenic region, a detection method and application. The specific marker is a nucleotide sequence of the non-insertion and insertion specific marker of the Oplegnathus punctatus recd / mtl5 intergenic region DNA fragment, wherein the non-insertion sequence is SEQ ID NO: 1, and the insertion sequence is the base shown in SEQ ID NO: 2. Based on the above-mentioned marker, the present application further designs a pair of specific primers: in individuals carrying the DNA insertion variation, two bands of 111 bp and 499 bp can be amplified simultaneously, and the band size difference is 388 bp; in individuals not carrying the insertion variation, only a single band of 111 bp can be amplified. The detection technology has important significance and broad application prospect in the application scenarios of Oplegnathus punctatus gender identification, high-male seed preparation and family selection breeding.
Owner:INST OF OCEANOLOGY - CHINESE ACAD OF SCI

RNA frameworks for gene editing and methods of gene editing

ActiveCN115044583BInsertion deletionProkaryote organisms
The application provides an RNA framework for gene editing and a gene editing method, the RNA framework comprising a sequence upstream of a target site, a sequence to be inserted, and a sequence downstream of the target site in the 5' to 3' direction. The gene editing method is based on the inherent mechanism of eukaryotes, uses RNP or RNA (which can be prepared in vitro) and related proteins as carriers, and is transferred into the cytoplasm and nucleus to realize gene editing on a specific sequence or site on the genome of a target system, such as insertion, deletion, replacement and site replacement of a specific sequence, and has high targeting accuracy. The application is more suitable for further clinical application than other prior art because no exogenous system or substance such as protein derived from prokaryotes is introduced, and no double-strand break is generated.
Owner:隋云鹏

Primary analysis in next generation sequencing

ActiveUS12469162B2Image analysisRecognition of DNA microarray patternBase callingData profiling
Image data analysis, particularly identifying cluster locations for performing base-calling in a digital flow cell image during DNA sequencing, is described. Each nucleic acid template molecule immobilized on a support may include an insert sequence and a sample index sequence. The sample index sequence may include a k-mer sequence. A sequencing system may conduct k cycles of sequencing reactions of the k-mer sequence before conducting one or more cycles of the insert sequence sequencing reactions and generate a first plurality of flow cell images. Pixel intensities may be determined for pixels of the first plurality of flow cell images. A base calling template may be determined and include base calling locations based on the pixel intensities and respective color purities of the pixel intensities. The base calling template may register a second plurality of flow cell images of the support in one or more cycles subsequent to the k cycles.
Owner:ELEMENT BIOSCIENCES INC

Nucleic acid editing system, and nucleic acid editing method and use

Provided in the present invention are a nucleic acid editing system, and a nucleic acid editing method and the use. The nucleic acid editing system comprises a framework structure and a cleavage structure. The framework structure comprises an upstream sequence of a target site, a sequence to be inserted and a downstream sequence of the target site; and the cleavage structure comprises an ORF2p protein and a derivative protein thereof. Further provided in the present invention are a nucleic acid editing method using the editing system; and the use of the editing system in the preparation of a drug for preventing and / or treating cancer, gene-related diseases or neurodegenerative diseases.
Owner:SUI YUNPENG

Pilot editing system, recombinant strain containing pilot editing system, application of recombinant strain and gene editing method

The invention relates to the field of gene engineering, and discloses a pilot editing system, a recombinant strain containing the pilot editing system, application of the recombinant strain and a gene editing method. The system comprises a coding gene of nicking enzyme nCas9, a coding gene of reverse transcriptase RT and pegRNA. Wherein the coding gene of the nicking enzyme nCas9 and the coding gene of the reverse transcriptase RT are connected through a Linker sequence, and the nucleotide sequence of the Linker sequence is as shown in SEQ ID NO. 1; the pegRNA comprises a gibberella zeylanica endogenous promoter 5SrRNA, sgRNA, a spacer sequence spacer, a primer binding site PBS (Phosphate Buffer Solution) and a reverse transcription template RT template; the reverse transcription template RT template carries an insertion sequence, and the insertion sequence is used for destroying the expression of a target gene. The method realizes efficient, accurate and safe gene editing of gibberella zeylanica, and has important scientific research and application values.
Owner:NANJING NORMAL UNIVERSITY +1

Single tube bead-based DNA co-barcoding for accurate and cost-effective sequencing, haplotyping, and assembly

Methods and compositions for preparing a nucleic acid sequencing library are described including (a) transposing an insertion sequence into first fragments of the target nucleic acid, wherein the insertion sequence comprises a hybridization sequence, and wherein the transposing produces nicks in the first fragments; (b) combining in a single mixture (i) the first fragments of the target nucleic acid from (a), (ii) a splint oligonucleotide, and (iii) a population of beads, wherein each bead comprises capture oligonucleotides immobilized thereon, and (c) ligating capture oligonucleotides of individual beads to inserted hybridization sequences of individual first fragments.
Owner:MGI TECH CO LTD

Indel marker PH-03-Indel-106 related to corn plant height character and application of index marker PH-03-Indel-106

The invention relates to the technical field of plant molecular breeding, in particular to an indel marker PH-03-Idel-106 related to the plant height character of corn and application of the indel marker PH-03-Idel-106 related to the plant height character of the corn, the Indel marker is located in the area of the third chromosome Chr3: 163962052-163964052 of the corn and is a 7bp insertion / deletion polymorphism marker, a 7bp insertion sequence CTGAGGG exists in a high-stalk corn inbred line, and no insertion sequence exists in a dwarf corn inbred line. A matched specific primer pair PH-03-Indel-106F / R can specifically amplify a target area, 1.5% agarose gel electrophoresis detection is carried out, it is judged that the corn plant height marker is a dwarf haplotype when a 270bp band appears, it is judged that the corn plant height marker is a high-stalk haplotype when no band exists, and the marker can be used for molecular marker-assisted selection, breeding improvement and early identification and screening of the corn plant height character. Phenotypes can be accurately predicted through DNA detection in the seedling stage, and environmental interference is avoided. The method has the advantages of being high in specificity, simple and convenient to detect, low in cost, high in throughput and the like, the breeding period can be remarkably shortened, directional improvement of the plant height character is achieved, and the method has important significance on corn variety genetic breeding and plant type optimization.
Owner:AGRICULTURAL GENOMICS INSTITUTE AT SHENZHEN CHINESE ACADEMY OF AGRICULTURAL SCIENCES (SHENZHEN BRANCH GUANGDONG LABORATORY FOR LINGNAN MODERN AGRICULTURE)

Single-tube bead-based DNA co-barcoding for accurate and economical efficient sequencing, haplotyping and assembly

Methods and compositions for preparing a nucleic acid sequencing library are described, the method comprising: (a) transposing an insertion sequence into a first fragment of a target nucleic acid, where the insertion sequence comprises a hybridization sequence, and where the transposing produces a nick in the first fragment; (b) combining (i) the first fragment of the target nucleic acid from (a), (ii) a splint oligonucleotide, and (iii) a population of beads wherein each bead comprises a capture oligonucleotide immobilized thereon, into a single mixture, and (c) linking the capture oligonucleotide of a single bead to an inserted hybridization sequence of a single first fragment.
Owner:MGI TECH CO LTD

Novel gene editing systems

PCT designated stageWO2025175355A1HydrolasesTransferasesInsertion sequenceNovel gene
The present disclosure relates to systems, vectors, and compositions for gene editing via the site-specific insertion of gene sequences, and methods of use thereof. In particular, the present disclosure relates to gene editing systems derived from insertion sequences and associated transposases.
Owner:THE UNIV OF SYDNEY

Method for continuously and gradually deleting gene promoters based on guide editing system

The invention relates to the technical field of biology, in particular to a method for continuously and gradually deleting gene promoters based on a guide editing system. The method for continuously and gradually deleting the gene promoter provided by the invention comprises the following steps: modifying ePE6d to obtain an ePE6d-dual35S vector, and driving the ePE6d-dual35S vector by a dual composite promoter 35S-CmYLCV-U6 in the ePE6d-dual35S vector to obtain a dual pegRNA expression cassette; the method comprises the following steps: selecting at least three NGG PAM sites and at least three CCN PAM sites in a starting region of a plant target gene, and editing and combining the NGG PAM sites and the CCN PAM sites; the method comprises the following steps: designing an sgRNA combination for each NGG PAM site and CCN PAM site to obtain NGG-pegRNA and CCN-pegRNA, inserting an NGG-pegRNA sequence into a double-pegRNA expression cassette, and inserting the CCN-pegRNA according to an editing combination to obtain a double-pegRNA vector library, finally transforming the double-pegRNA vector library into a plant cell, and deleting plant target gene promoter fragments to obtain a mutant library which is continuously and gradually deleted. According to the method provided by the invention, the promoter truncation mutants with different lengths can be obtained.
Owner:ANHUI AGRICULTURAL UNIVERSITY

Functional marker for melon gummy stem resistance and use thereof

The application discloses a functional marker for identifying resistance to melon vine blight, and belongs to the technical field of molecular marker assisted breeding. The marker is located in the CDS region of a melon vine blight resistance gene, is an InDel molecular marker, and has a nucleotide sequence as shown in SEQ ID NO:1, and has a total length of 197 bp. The marker has a 9 bp base insertion sequence difference with a susceptible material. The application further discloses a method for identifying resistance to melon vine blight by using the functional marker. The application can be used for identifying melon vine blight resistant germplasm materials, and has important application value in melon vine blight resistance breeding and functional marker assisted selection.
Owner:HUAZHONG AGRI UNIV

Methods for reprogramming and gene editing cells

The present disclosure provides improved methods for reprogramming and gene editing cells. In one aspect, the present disclosure provides a method of introducing a single strand break in a DNA site. In one aspect, the present disclosure provides a method of inserting a sequence in a DNA site by introducing a single strand break followed by insertion of the sequence using a single-stranded repair template. In another aspect, the present disclosure provides a method of activating gene expression in a cell during its differentiation. In another aspect, the present disclosure methods and compositions related to iPSC-derived mesenchymal stroma / stem cells that overexpressed IDO1. In another aspect, the present disclosure provides a solid support comprising iPSC-derived mesenchymal stem cells which can be used to treat organ damage.
Owner:FACTOR BIOSCIENCE INC

Recombinant vectors for preparing hla / beta2m complex and methods of making and using the same

ActiveCN116004718Beffective stimulationPlay a role in cancer treatmentAntinoxious agentsFermentationAntiendomysial antibodiesSpecific enzyme
The application discloses a recombinant carrier for preparing HLA / beta 2M complex and a preparation method and application thereof, relates to the technical field of antibody preparation of MHC-polypeptide complex, and provides a recombinant carrier for preparing HLA / beta 2M complex, wherein FOS leucine zipper bZIP motif is inserted between NheI / AvrII enzyme cutting sites of an original carrier, JUN leucine zipper bZIP motif is inserted between BsiWI / BlpI enzyme cutting sites, beta 2M gene sequence is inserted between AgeI / NheI enzyme cutting sites, and HLA sequence is inserted between specific enzyme cutting sites, so that the prepared HLA / beta 2M complex has high expression, and the highest expression reaches 92.45 mg / L.
Owner:PUJIAN BIOLOGICAL (WUHAN) TECH CO LTD

A method for rapid identification of exogenous insertion sequences based on whole genome sequencing data

This invention provides a method for rapidly identifying exogenous inserted sequences based on whole-genome sequencing data, comprising the following steps: sequencing data quality control, preliminary data alignment, screening of preliminary alignment results, evaluation of secondary alignment results, homology detection, preliminary insertion region detection, precise insertion site identification, assembly of inserted and flanking sequences, acquisition of genes affected by the insertion site, and primer design for the insertion site. Compared with traditional experimental detection techniques, this invention is less time-consuming, reproducible, and presents more comprehensive transgenic insertion characteristics; compared with other existing whole-genome resequencing methods, it is more accurate and intuitive, the results are easier to understand, and it is more conducive to the safety risk assessment of transgenic plants and animals, thus contributing to the development and application of transgenic or gene editing technologies.
Owner:WUHAN WANMO TECH CO LTD

Muscle-targeted adeno-associated virus capsid protein, adeno-associated virus containing same, vector and application

The invention provides a muscle-targeted adeno-associated virus capsid protein, an adeno-associated virus containing the muscle-targeted adeno-associated virus capsid protein, a vector and application. The present disclosure provides an adeno-associated virus capsid protein, which comprises a targeting peptide, and the targeting peptide comprises any one of the following amino acid sequences: SEQ ID NO: 1-19. According to the invention, a reasonable design and directed evolution combined method is adopted, and on the basis of a receptor integrin-RGD polypeptide specific binding principle, random amino acids are carried to adapt to construction and screening of the AAV vector of a capsid structure, so that the problems of poor stability of the capsid structure, change of histocompatibility and the like caused by direct insertion of a sequence are avoided; therefore, efficient transduction of muscular tissues is realized, and a reliable platform is provided for gene therapy.
Owner:INNOVEC BIOTHERAPEUTICS

A dual-carrier system for treating hearing loss and its application

The present invention belongs to the field of gene therapy within the medical field, and specifically involves the use of overexpression of normal genes to restore hearing in patients with hereditary deafness caused by gene mutation or deletion. The present invention provides a dual-vector system for expressing the OTOF protein, comprising two nucleotide sequences: a first nucleotide sequence comprising two ITR sequences and a gene expression cassette inserted between the ITR sequences; and a second nucleotide sequence comprising two ITR sequences and a gene expression cassette inserted between the ITR sequences. The gene expression cassette of the first nucleotide sequence comprises a promoter, an OTOF N-terminal coding sequence, an intein N-terminal coding sequence, and polyA; and the gene expression cassette of the second nucleotide sequence comprises a promoter, an intein C-terminal coding sequence, an OTOF C-terminal coding sequence, and polyA. Also provided is an adeno-associated virus packaged by the aforementioned vector. The vector and virus can be used in the field of large-gene dual-vector delivery for gene therapy for deafness to restore hearing in both ears through unilateral administration.
Owner:上海佑音医药生物科技有限公司

Compositions and methods for generating circular RNA

Compositions and methods for producing a circular RNA (circRNA) are provided. Nucleic acid molecules, such as RNA molecules, comprising a ribozyme and an insertion sequence are provided. In some aspects, ribozyme in an RNA molecule is cleaved. In some embodiments, the cleaved RNA molecule is cyclized by a ligase. Also provided are methods and systems for producing the circular RNA, as well as methods of using the circular RNA, including therapeutic and prophylactic methods.
Owner:ST PHARM CO LTD

Plant genetic transformation system based on direct delivery, genetic transformation method and application

The invention relates to the technical field of plant genetic transformation, and provides a plant genetic transformation system based on direct delivery, a genetic transformation method and application. An original vector pMKV057 is directionally modified to obtain a modified vector, and the modification method comprises the following steps: replacing an LUC expression cassette of the vector with a modular expression cassette integrated with an epitope tag; the method comprises the following steps: designing multiple cloning sites on a vector, introducing restriction enzyme cutting sites HindIII and EcoRI or HindIII and XbaI, and inserting a Kozak sequence into a 5'end upstream adjacent region of a nucleotide sequence of the multiple cloning sites to obtain a modified vector. And transforming the modified vector into agrobacterium tumefaciens to carry out plant genetic transformation. Through the technical scheme, the problems of low plant genetic transformation efficiency and long transformation time in related technologies are solved.
Owner:YAZHOUWAN NATIONAL LABORATORY +1