摘要:
A plant cell comprising at least one modification which modulates the expression or activity of polynucleotides or polypeptides homologous to SEQ ID NOs: 1-4. A method for producing a plant with modulated expression or activity of polynucleotides or polypeptides homologous to SEQ ID NOs: 1-4. Plants with modulated alkaloid concentrations, and methods for their production.
摘要:
The technology provided herein relates to methods for the delivery of pre-assembled ribonucleoprotein complexes (RNP) - such as the Cas9/gRNA RNP complex - for highly efficient genome editing to intact differentiated cells and regeneration of cell lines, whole tissues or organisms thereof.
摘要:
The current invention relates to methods of targeted genetic alteration in plant cells, as well as to plant cells and plants thus obtained. In the method, the use of the combination of a nickase and a single-stranded oligonucleotide of the invention, provides for targeted alteration of a DNA duplex with increased efficacy.
摘要:
A Solanaceous plant exhibiting a facultative parthenocarpy is provided. The plant comprises a loss-of-function mutation in a Sl AGL6 gene and alternatively or additionally characterized by an average fruit weight/plant at least about the same as that of a non-parthenocarpic tomato of the same genetic background under fertilization permissive conditions of the non-parthenocarpic tomato. Also provided are methods of producing such plants and processed products produced from same.
摘要:
Described are methods and materials for the genetic modification of plants by specific gene targeting and precise editing of nucleic acid sequences in a plant. The methods and materials provided herein enable one to edit the plant genome by design to control the expression of endogenous genes and/or control the transmission and expression of transgenic traits. Provided are also methods of producing plants having a desirable agronomic trait by crossing a transgenic plant expressing a gRNA with a plant expressing a Cas enzyme, and selecting a progeny plant having the desirable agronomic trait or a seed thereof.
摘要:
Compositions and methods are provided producing a complex trait locus in a genomic window of a soybean plant comprising (i) at least one transgenic target site for site specific integration integrated in at least double-strand-break target site, (ii) at least one double-strand-break target site and at least one transgene, (iii) at least one altered double-strand-break target site or (iv) any one combination of (i)-(iii). The double-strand-break target site can be, but is not limited to, a target site for a zinc finger endonuclease, an engineered endonuclease, a meganuclease, a TALENs and/or a Cas endonuclease. The genomic window of said plant can comprise at least one genomic locus of interest such as a trait cassette, a transgene, a mutated gene, a native gene, an edited gene or a site-specific integration (SSI) target site.
摘要翻译:提供了在大豆植物的基因组窗口中产生复合性状基因座的组合物和方法,其包含(i)至少一个用于位点特异性整合的转基因靶位点,其整合于至少双链断裂靶标 (ii)至少一个双链断裂靶位点和至少一个转基因,(iii)至少一个改变的双链断裂靶位点或(iv)(i) - (iii)的任何一种组合, 。 双链断裂靶位点可以是但不限于锌指内切核酸酶,工程内切核酸酶,大范围核酸酶,TALEN和/或Cas核酸内切酶的靶位点。 所述植物的基因组窗口可以包含至少一个感兴趣的基因组基因座,例如性状盒,转基因,突变的基因,天然基因,编辑的基因或位点特异性整合(SSI)靶位点。 p >
摘要:
본 발명은 Cas 단백질-가이드 RNA RNP (ribonucleoprotein)를 이용하여 식물 원형질체로부터 재생된 유전체가 교정된 식물체의 제조 효율을 증가시키는 방법에 관한 것이다. 본 발명의 유전체 교정 식물체의 제조 효율을 증가시키는 방법을 통해 표적 유전자가 변이된 식물체를 효율적으로 생산할 수 있을 뿐 아니라, 식물체 내 외래 DNA의 삽입을 최소화할 수 있다. 따라서 본 발명은 농업, 식품 및 생명공학분야 등 다양한 분야에서 매우 유용하게 사용될 수 있다.
摘要:
A method for obtaining glyphosate-resistant rice by a site-directed nucleotide substitution is provided, which comprises the following steps: only substituting threonine (T) at position 8 of the amino acid sequence of a conserved region of endogenous EPSPS protein of a target plant with isoleucine (I), and substituting proline (P) at position 12 with serine (S) to obtain a plant, i.e., a glyphosate-resistant plant. A method capable of generating a site-directed nucleotide substitution and a fragment substitution utilizing a CRISPR-mediated NHEJ pathway to substitute a region between two gRNA sites by designing the two gRNA sites is provided.
摘要:
Provided is a method for conducting site-specific modification in a plant through gene transient expression, comprising the following steps: transiently expressing a sequence-specific nuclease specific to the target fragment in the cell or tissue of the plant of interest, wherein the sequence-specific nuclease is specific to the target site and the target site is cleaved by the nuclease, thereby the site-specific modification of the target site is achieved through DNA repairing of the plant.
摘要:
A nucleic acid construct is provided. The construct comprises a tobacco rattle virus (TRV) sequence and a nucleic acid sequence encoding a single guide RNA (sgRNA) that mediates sequence-specific cleavage in a target sequence of a genome of interest, wherein the TRV sequence is devoid of a functional 2b sequence. Also provided are plant cells comprising the construct and uses of the construct in gene editing.