A01H1/022

METHOD FOR IDENTIFYING WHETHER A DIPLOID POTATO IS SELF-COMPATIBLE
20220298549 · 2022-09-22 ·

The present application relates to the technical field of genetic breeding, and provides a method for identifying whether a diploid potato is self-compatible. The method relates to identifying whether a StSCI gene in the diploid potato is transcribed and expressed. Also disclosed is a method for identifying whether a StSCI gene is expressed by using molecular marker, and a method of screening for the molecular marker, which includes: obtaining the genome sequence information of parental materials, screening for difference sites of the parental materials, screening for the molecular marker, and identifying whether the screened molecular marker are usable. As for the identification of the self-compatibility of a diploid potato by using the screened molecular marker, the identification workload is small, a lot of time is saved, and the identification result is not affected by the environment, and it is accurate and reliable.

STSCI PROTEIN FOR CHANGING SELF-INCOMPATIBILITY OF DIPLOID POTATO MATERIALS
20220298526 · 2022-09-22 ·

Provided is a StSCI protein for changing the self-incompatibility of diploid potato materials, wherein the amino acid sequence of the StSCI protein includes or consists of the following sequence: 1) the amino acid sequence represented by SEQ ID NO: 1; or 2) a functional homologous sequence having at least 95% sequence identity with the amino acid sequence represented by SEQ ID NO: 1; or 3) a protein in which one or more (e.g., 1-10) amino acids are added, deleted, or replaced in the amino acid sequence represented by SEQ ID NO: 1 and has the activity of inhibiting self-incompatibility. The advantage of the application is that the StSCI protein may inhibit the cytotoxicity of multiple types of S-RNase, which is hereditary and fundamentally overcomes the defect of self-incompatibility of diploid potatoes, thereby facilitating to realize the cultivation of a high-generation homozygous inbred line of diploid potatoes.

Methods of crossbreeding fungi organisms
11419280 · 2022-08-23 ·

Methods of crossbreeding fungi organisms. The methods include placing a first fungus organism on a first growth medium. The first fungus organism is selected from the genus Psilocybe or Panaeolus. The methods further include placing a second fungus organism on the first growth medium adjacent to the first fungus organism. The second fungus organism is selected from the genus Psilocybe or Panaeolus and is different than the first fungus organism. The methods include allowing the first fungus organism to replicate to form a first colony and allowing the second fungus organism to replicate to form a second colony. The methods further include allowing the first colony and the second colony to expand until they intersect along a clamp line where the first colony and the second colony exchange genetic material between them to yield a crossbred fungus organism.

EMBRYOGENESIS FACTORS FOR CELLULAR REPROGRAMMING OF A PLANT CELL

Plant cell fate and development is altered by treating cells with cellular reprogramming factors. Embryogenesis inducing embryogenesis factor genes and/or morphogenic developmental genes are used as cellular reprogramming factors, specifically comprising polypeptides or polynucleotides encoding gene products for generating doubled haploids or haploid plants from gametes. Maize microspores treated by contacting the isolated cells with an exogenous purified, recombinant embryogenesis inducing embryogenesis factor gene products and/or morphogenic developmental gene polypeptide results in embryogenesis. The gametes of a maize plant develop into embryoids when transformed with a genetic construct including regulatory elements and structural genes capable of acting in a cascading fashion to alter cellular fate of plant cells. Embryogenesis factor proteins and/or developmental morphogenic proteins expressed from a genetic construct are used for ex situ treatment methods and for in planta cellular reprogramming.

WHEAT MS1 POLYNUCLEOTIDES, POLYPEPTIDES, AND METHODS OF USE

Compositions and methods are capable of modulating male fertility in a plant. Compositions comprise polynucleotides and polypeptides, and fragments and variants thereof, which modulate male fertility. Expression cassettes comprise a male-fertility polynucleotide, or fragment or variant thereof, operably linked to a promoter, wherein expression of the polynucleotide modulates the male fertility of a plant. The level and/or activity of a polynucleotide that influences male fertility is modulated in a plant or plant part. Regulatory sequences drive expression in a male-tissue-preferred manner and may be targets to downregulate an operably linked gene. Methods to track mutations that induce nuclear recessive male sterility in subsequent selfing and crossing of wheat lines containing the mutations are also provided. Male-sterile plants may be maintained by pollinating with a maintainer plant.

Plants Producing 2N Gametes or Apomeiotic Gametes

The invention relates to plants wherein the protein OSD1, involved in the transition from meiosis I to meiosis II is inactive. These plants produce Second Division Restitution (SDR) 2n gametes. The invention further relates to plants wherein the inactivation of OSD1 is combined with the inactivation of a gene involved in meiotic recombination in plants, and of a gene involved in the monopolar orientation of the kinetochores during meiosis. These plants produce apomeiotic gametes. These plants are useful in plant breeding.

Wheat MS1 polynucleotides, polypeptides, and methods of use

Compositions and methods are capable of modulating male fertility in a plant. Compositions comprise polynucleotides and polypeptides, and fragments and variants thereof, which modulate male fertility. Expression cassettes comprise a male-fertility polynucleotide, or fragment or variant thereof, operably linked to a promoter, wherein expression of the polynucleotide modulates the male fertility of a plant. The level and/or activity of a polynucleotide that influences male fertility is modulated in a plant or plant part. Regulatory sequences drive expression in a male-tissue-preferred manner and may be targets to downregulate an operably linked gene. Methods to track mutations that induce nuclear recessive male sterility in subsequent selfing and crossing of wheat lines containing the mutations are also provided. Male-sterile plants may be maintained by pollinating with a maintainer plant.

CANNABIS VARIETY WHICH PRODUCES GREATER THAN 50% FEMALE PLANTS
20210144947 · 2021-05-20 ·

According to the invention, there is provided a novel hemp Cannabis cultivar which produces a skewed ratio of female plants. This invention thus relates to the seeds of hemp Cannabis cultivar of the invention, to the plants of hemp Cannabis cultivar of the invention, to plant parts of hemp Cannabis cultivar of the invention, to methods for producing a Cannabis cultivar by crossing the hemp Cannabis cultivar of the invention with another Cannabis cultivar, and to methods for producing a Cannabis cultivar containing in its genetic material one or more backcross conversion traits or transgenes and to the backcross conversion Cannabis plants and plant parts produced by those methods.

GENETIC LOCI ASSOCIATED WITH INCREASED FERTILITY IN MAIZE

The present invention relates to methods and compositions for identifying, selecting and/or producing a maize plant or plant part having increased fertility. A maize plant or plant part that has been identified, selected and/or produced by any of the methods of the present invention is also provided.

METHODS AND COMPOSITIONS RELATING TO MAINTAINER LINES

The methods and compositions described herein relate to maintainer lines (e.g, male-fertile lines) for producing or propogation of plants with a male-sterile phenotype.