How is waste excreted in paramecium?
The food vacuole filled with undigested matter fuses with the cell membrane at a site called Cytoproct from where it will be expelled out. Excretion in Paramecium is carried out by the Contractile vacuoles. There are two contractile vacuoles in paramecium present at both the ends of the body.
What is the excretory organ of paramecium?
What type of structure does paramecium use for movement?
What is the structure and function of paramecium?
The body of a paramecium is asymmetrical. It has a well-defined ventral or oral surface and has a convex aboral or dorsal body surface. Its whole body is covered with a flexible, thin and firm membrane called pellicles. These pellicles are elastic in nature which supports the cell membrane.
Is Volvox a plant or animal cell?
Straddling the plant and animal kingdoms, the protist Volvox forms stunning bright green colonial balls in water bodies that are enriched in nitrates. Found in puddles, ditches, shallow ponds and bogs, Volvox colonies reach up to 50,000 cells and may include daughter and granddaughter colonies.
What are Kappa particles?
Kappa organism, also called Kappa Particle, gram-negative symbiotic bacterium found in the cytoplasm of certain strains of the protozoan Paramecium aurelia. These bacteria, when released into the surroundings, change to P particles that secrete a poison (paramecin) that kills other sensitive strains of P. aurelia.
What is Extrachromosomal inheritance?
Vertical transmission of hereditary characters by DNA from cytoplasmic organelles such as MITOCHONDRIA; CHLOROPLASTS; and PLASTIDS, or from PLASMIDS or viral episomal DNA.
Who discovered Kappa particles in paramecium?
What is killer paramecium?
Paramecium strains possessing the particles are known as “killer paramecia”. They liberate a substance also known as paramecin into the culture medium that is lethal to Paramecium that do not contain kappa particles. Kappa particles are found in genotypes of Paramecium aurelia syngen 2 that carry the dominant gene K.
What is an example of cytoplasmic inheritance?
The inheritance of characters controlled by genes present in the cell cytoplasm rather than by genes on the chromosomes in the cell nucleus. An example of cytoplasmic inheritance is that controlled by mitochondrial genes (see mitochondrion).
What is cytoplasmic inheritance in genetics?
Extranuclear inheritance or cytoplasmic inheritance is the transmission of genes that occur outside the nucleus. It is found in most eukaryotes and is commonly known to occur in cytoplasmic organelles such as mitochondria and chloroplasts or from cellular parasites like viruses or bacteria.
Which is responsible for cytoplasmic inheritance?
What is Extrachromosomal inheritance explain with an example?
“A non-mendelian pattern of inheritance governed by the DNA present in the cytoplasm is known as extrachromosomal inheritance or cytoplasmic inheritance.” Nuclear DNA is the basis for inheritance of almost all type of phenotype of ours. It inherited in a particular fashion from parents to their offspring.
Which parent contributes more in cytoplasmic inheritance?
What is maternal effect inheritance?
In genetics, a maternal effect occurs when the phenotype of an organism is determined by the genotype of its mother. Because of the inheritance pattern of maternal effect mutations, special genetic screens are required to identify them.
What is Biparental inheritance?
(2) A type of extranuclear inheritance, in which both parents contribute organellar DNA to the progeny, as occurs in biparental mitochondrial inheritance in Saccharomyces cerevisiae (a yeast). …
What is the difference between cytoplasmic inheritance and genetic maternal effect?
The key difference between cytoplasmic inheritance and genetic maternal effect is that cytoplasmic inheritance occurs due the genetic information stored in genes of some organelles such as mitochondria and chloroplasts present in the cytoplasm while genetic maternal effect occurs due to the mRNA and proteins received …
What is the difference between genetic maternal effect and genomic imprinting?
In genetic maternal effect, the phenotypes of the progeny are determined by the genotype of the mother only. In genomic imprinting, the phenotype of the progeny differs based on whether a particular allele is inherited from the mother or the father.
What is imprinting in genetics?
Genomic imprinting is an epigenetic phenomenon that causes genes to be expressed in a parent-of-origin-specific manner. These epigenetic marks are established (“imprinted”) in the germline (sperm or egg cells) of the parents and are maintained through mitotic cell divisions in the somatic cells of an organism.
What is the role of maternal effect gene in Drosophila?
The maternal effect genes are responsible for the polarity of the egg and of the embryo. The developing egg (oocyte) is polarized by differentially localized mRNA molecules. Nanos and Caudal are maternal effect genes that are important in the formation of more posterior abdominal segments of the Drosophila embryo.
Where are maternal effect genes located?
Maternal-Effect Genes Maternal genes are those genes whose products, RNA or protein, are produced or deposited in the oocyte or are present in the fertilized egg or embryo before expression of zygotic genes is initiated.