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40 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.

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

Modified bacterial strains

PCT designated stageWO2025219556A1Microorganism based processesNucleic acid reductionMicrobiologyBacterial strain
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

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

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

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

Recombinant adeno-associated virus particle containing targeted transcriptional melittin gene as well as preparation method and application of recombinant adeno-associated virus particle

The invention belongs to the technical field of biological medicines, and provides a recombinant adeno-associated virus particle containing a targeted transcriptional melittin gene as well as a preparation method and application of the recombinant adeno-associated virus particle. Wherein the expression cassette containing the targeted transcriptional melittin gene contains a human telomerase reverse transcriptase core promoter, a tetracycline response element, an optimized melittin gene, a ribosome insertion sequence and a human enterokinase light chain-melittin fusion gene. The invention aims to solve the problem of how to realize precise targeted therapy of tumors, effectively kill tumor cells, reduce damage to normal cells to the greatest extent, overcome the limitation of a traditional treatment method and solve the problem of packaging cell death caused by advanced transcription of melittin genes in a recombinant AAV packaging process. And it is ensured that melittin expressed in tumor cells has a natural sequence and activity, and a safer and more effective treatment choice is provided for tumor patients.
Owner:SHANXI UNIV

A method for screening high-transmission risk drug-resistant plasmids based on exogenous capture

PendingCN122629167AReceptorInsertion sequence
The application discloses a high-transmission-risk drug-resistant plasmid screening method based on exogenous capture, which comprises the following steps: collecting environmental source samples and preparing a donor bacterial population suspension, preparing a plasmid-negative E. coli receptor bacterial suspension with identifiable markers or selectable resistance markers, performing exogenous conjugation culture through a filter membrane conjugation method, screening candidate conjugants by combining a background screening antibiotic with a target screening antibiotic, performing multi-antibiotic phenotype primary screening on the candidate conjugants, extracting plasmid DNA of target conjugants and performing high-throughput sequencing, identifying plasmid-related sequences and performing redundancy removal processing, and then performing replica type, drug resistance gene, potential virulence-related gene, heavy metal resistance-related gene, disinfectant resistance-related gene and insertion sequence-related element multi-dimensional characteristic analysis on representative samples, and finally comprehensively screening high-transmission-risk drug-resistant plasmids.
Owner:INST OF URBAN ENVIRONMENT CHINESE ACAD OF SCI

Recombinant adeno-associated viruses and uses thereof

PCT designated stageWO2025217214A3VectorsGenetic material ingredientsHeterologousInsertion sequence
The present invention relates to recombinant adeno-associated viruses (rAAVs) having capsid proteins engineered to include amino acid sequences that confer and / or enhance desired properties. In particular, the invention provides engineered capsid proteins comprising peptide insertions from heterologous proteins inserted within or near variable region IV (VR-IV) or variable region VIII (VR-VIII) of the virus capsid, such that the insertion is surface exposed on the AAV particle. The invention also provides capsid proteins that direct rAAVs to target tissues, in particular, capsid proteins comprising peptides that are inserted into surface-exposed variable regions using a method for replacing a stop codon in the capsid gene with such peptide insert. The invention provides such methods for making the rAAV vectors into vector libraries and selecting the rAAV vectors having peptide inserts that target the rAAV to particular tissues of interest, and thus deliver therapeutics for treating disorders.
Owner:REGENXBIO INC

Polypeptide comprising a capsid protein sequence

PCT designated stageWO2025233437A1Peptide/protein ingredientsVirus peptidesInsertion sequenceCapsid
The present invention discloses a polypeptide comprising a capsid protein sequence consisting of eight core regions and seven loop modification regions, wherein the eight core regions are defined, respectively, by amino acid positions M1 to S309, P319 to R328, T340 to T342, M349 to F352, W359 to F362, V368 to Q373, T383 to T387 and T392 to N644 in the amino acid sequence according to SEQ ID NO: 1, wherein the eight core regions of the capsid protein sequence have at least 70 % sequence identity to the eight core regions of the amino acid sequence according to SEQ ID NO: 1 or SEQ ID NO: 2 at least in the range from R32 to N570, wherein the seven loop modification regions are defined, respectively, by amino acid positions A310 to I318, H329 to I339, I343 to T348, D353 to E358, A363 to D367, T374 to A382, and A388 to V391 in the amino acid sequence according to SEQ ID NO: 1, wherein at least one loop modification region of the capsid protein sequence differs from the corresponding loop modification region of the amino acid sequences according to SEQ ID NO: 1 and SEQ ID NO: 2 at least in that the at least one loop modification region comprises - a peptide insert sequence comprising at least 3 amino acids, so that the at least one loop modification region of the capsid protein sequence is extended with respect to the corresponding loop modification region of the amino acid sequences according to SEQ ID NO: 1 and SEQ ID NO: 2 by said number of amino acids; and / or - a cysteine residue, and Virus-like Nanoparticles (VLNPs) comprising such polypeptides.
Owner:A-SPECTAR GMBH

Universal insertion sequence and application thereof in preparation of multiplex PCR template nucleic acid

The invention discloses a universal insertion sequence and application thereof in preparation of multiple PCR template nucleic acid. The invention provides a universal insertion sequence and a method for preparing multiple PCR template nucleic acid based on the universal insertion sequence, and the method comprises the following steps: firstly, designing universal insertion sequences with different GC contents, and distributing a universal insertion sequence with similar GC content for each multiple PCR target amplicon; the method comprises the following steps: firstly, synthesizing a universal insertion sequence primer, then synthesizing a hybrid PCR primer containing the universal insertion sequence primer and a multiplex PCR target amplicon primer, and introducing the multiplex PCR target amplicon into the universal insertion sequence through one-step PCR amplification, so as to obtain a set of artificial chimeric DNA template containing the multiplex PCR primer, and the artificial chimeric DNA template can be used as multiplex PCR template nucleic acid for developing and optimizing a multiplex PCR system.
Owner:BEIJING CAPITALBIO MEDLAB CO LTD

Method for breeding high-yield green-shell laying hens by using PGC gene editing technology

The invention provides a method for breeding high-yield green-shell laying hens by using a PGC gene editing technology, and belongs to the field of poultry breeding and gene engineering. According to EAV-HP insertion site information of a 5'flanking region of an SLCO1B3 gene, a group of sgRNA aiming at the gene region and a donor DNA template containing an EAV-HP insertion sequence and a regulatory element are designed and obtained. An EAV-HP sequence is directionally introduced into a chicken primordial germ cell genome by utilizing a CRISPR / Cas9 system, successfully edited cells are screened out and cultivated into gene edited chickens, and a new strain of laying hens capable of stably inheriting and laying green-shell eggs is established through a generation of breeding, so that the economic benefit of commercial laying hen breeding is remarkably improved.
Owner:刘小军

A transposon insertion variant detection and classification method based on long read sequencing data and related devices

The present application belongs to the technical field of transposon insertion variation, and relates to a transposon insertion variation detection and classification method based on long read sequencing data and a related device. The method comprises: obtaining long read sequencing data and aligning the data with a reference genome; extracting alignment signals and locating candidate insertion regions; obtaining high-confidence insertion events through multi-stage clustering and refining; extracting and standardizing insertion sequence fragments; converting the sequences into numerical features; using a deep learning model to annotate the insertion types, outputting transposon type probabilities; and finally comparing the likelihood values of different genotype hypotheses, selecting the maximum probability genotype and calculating the genotype quality score. The present application solves the problems of low calculation efficiency of traditional sequence alignment-based annotation methods and insufficient accuracy and robustness of sequence classification methods based on large models, and realizes efficient and accurate transposon insertion variation detection and genotype determination.
Owner:XI AN JIAOTONG UNIV

An enhancer sv molecular marker for regulating sheep body size, a detection method thereof and breeding application

PendingCN122629214AInsertion sequenceLuciferases
The application discloses an enhancer SV molecular marker for regulating sheep body size, a detection method thereof and breeding application. F ST The selection signal analysis is combined with gene and site annotation to screen out a key SV site molecular marker affecting the body size. The marker is located at 77414842 bp of an IGFBP3 gene on a sheep chromosome 4, and is a 51 bp insertion variation. Sheep individuals carrying the insertion sequence are small in body size, and sheep individuals not carrying the insertion sequence are large in body size. The application adopts a double luciferase reporter system to detect and verify the functional effect of the variation, and the result shows that the luciferase activity of a recombinant vector containing the insertion fragment is significantly higher than that of an empty control, and the relative expression amount is 2.4, which indicates that the insertion variation has a regulating influence on the sheep body size by significantly enhancing the transcription activity of the IGFBP3 gene. The molecular marker can be applied to early body size selection of sheep, and can accelerate the breeding process of meat sheep.
Owner:LANZHOU UNIV

KASP molecular marker of nbeds1 gene, detection method and application thereof

PendingCN122382244ADiseaseMutant allele
The application relates to a KASP molecular marker of an NbEDS1 gene, a detection method and application, and belongs to the technical field of plant molecular breeding. The KASP molecular marker is designed according to a specific 97 bp InDel site in a Nicotiana benthamiana NbEDS1 gene mutant, the wild-type allele is C (containing a 97 bp insertion sequence), the mutant allele is A (the insertion sequence is deleted), the marker has the advantages of high specificity, fast detection speed, low cost, high throughput and high accuracy, and can be applied to genotype identification of the NbEDS1 gene mutant of the Nicotiana benthamiana, rapid screening of mutant materials in related research on a TNL type immune receptor disease resistance pathway, and genetic analysis and breeding selection related to the NbEDS1 gene.
Owner:YUNNAN ACAD OF TOBACCO AGRI SCI

Starfish gender-related in del molecular marker, primer and application thereof

ActiveCN121951020BZooidNucleotide
The present application relates to a kind of star point oriental tile genetic sex related InDel molecular marker, primer and its application, belong to molecular biology field, the molecular marker is located on the male DNA of star point oriental tile, the partial DNA sequence shown in the molecular marker is as shown in SEQ ID NO.1, the InDel molecular marker is a 2bp length insertion sequence, at the 35th and 36th of nucleotide sequence shown in SEQ ID NO.1, the sequence only stably exists in the genome of male individual of star point oriental tile, is deleted in the genome of female individual.This application can accurately and non-invasively identify the genetic sex of star point oriental tile fry and non-breeding season adult fish without killing experimental subjects.
Owner:YELLOW SEA FISHERIES RES INST CHINESE ACAD OF FISHERIES SCI

Recombinant adeno-associated viruses and uses thereof

PCT designated stageWO2025217214A2VectorsGenetic material ingredientsHeterologousInsertion sequence
The present invention relates to recombinant adeno-associated viruses (rAAVs) having capsid proteins engineered to include amino acid sequences that confer and / or enhance desired properties. In particular, the invention provides engineered capsid proteins comprising peptide insertions from heterologous proteins inserted within or near variable region IV (VR-IV) or variable region VIII (VR-VIII) of the virus capsid, such that the insertion is surface exposed on the AAV particle. The invention also provides capsid proteins that direct rAAVs to target tissues, in particular, capsid proteins comprising peptides that are inserted into surface-exposed variable regions using a method for replacing a stop codon in the capsid gene with such peptide insert. The invention provides such methods for making the rAAV vectors into vector libraries and selecting the rAAV vectors having peptide inserts that target the rAAV to particular tissues of interest, and thus deliver therapeutics for treating disorders.
Owner:REGENXBIO INC

Takifugu star genetic sex related InDel molecular marker, primer and application thereof

The invention relates to an InDel molecular marker related to genetic sex of Takifugu stellate, a primer and application thereof, and belongs to the field of molecular biology, the molecular marker is located on male DNA of Takifugu stellate, the DNA sequence of the part where the molecular marker is located is as shown in SEQ ID NO.1, the InDel molecular marker is an insertion sequence with the length of 2bp, and at the 35th site and the 36th site of the nucleotide sequence as shown in SEQ ID NO.1, the nucleotide sequence of the primer is as shown in SEQ ID NO.1. The sequence only stably exists in male individual genomes of Takifugu star and is deleted in female individual genomes. According to the method disclosed by the invention, the genetic sex of the fugu stellus fries and the adult fishes in the non-breeding season can be accurately and noninvasively identified on the premise of not killing experimental subjects.
Owner:YELLOW SEA FISHERIES RES INST CHINESE ACAD OF FISHERIES SCI