Genetics Flashcards
Define gene?
Is a unit if genetic information that gives instructions on how to make protein and is made of DNA
What is genetics?
It is the study of hereditary and variation , it involves I hesitance of physical and biological characteristics from the parent to offspring by the help of genes and alleles
What is DNA?
DNA stores all genetics information in a cell , specific segments of DNA called genes encode for the production of protein
What is chromosome?
Chromosomes are very long, coiled pieces of DNA, which can be easily copied and pass on genetic information during cell division.
What is genotype?
Genotype is the combination of alleles an organism has for a particular trait or for all traits.
What is the phenotype?
Phenontype is the observable physical, or biochemical characteristics that organism has, which are influenced by both its genotype and environment.
What is Dominant trait / allele ?
Fully expressed in the genotype and phenotype of an organism because the dominant allele masks the effect of recessive allele in the genotype
What is recessive trait / allele?
Recessive allele is partially expressed or not expressed in the genotype or phenotype of an organism. It is only expressed if it is homozygous recessive
What is homozygous?
Is the true breeding whereby there are 2 identical alleles for a particular trait and it has only has dominant or recessive allele (not both at once) and it produces 1 type of gamete
What is heterozygous?
Heterozygous is where an organism has two different alleles for a particular gene — one dominant and one recessive and it produces 2 types of gamete
How many type of gametes does homozygous produce?
1 types
How many type of gametes does heterozygous produce?
2 type
List 3 difference between homozygous and heterozygous
Homozygous
- Heterozygous means an organism has two different alleles for a particular gene — one dominant and one recessive.
- it produces only 1 type of gamete
- both the alleles are similar eg RR rr
WHEREAS
heterozygous
-Heterozygous means an organism has two different alleles for a particular gene — one dominant and one recessive.
- produces 2 type of gamete
- alleles are not similar eg Rr
What is haploid cell?
A haploid cell is a cell that contains only one chromosome from each homologous pair, meaning it has a single set of chromosomes and only one allele for each gene. Examples include gametes such as sperm and egg cells, and pollen grains.
What is diploid cell?
A diploid cell is a cell that contains full sets of homologous chromosomes, one set inherited from each parent. It has two alleles for each gene, one from each parent, which together code for each trait. Examples of diploid cells include somatic cells, such as liver and muscle cells.
What is Homologous Pair?
Homologous refers to chromosomes that are similar in size, shape, and carry the same genes, with one chromosome coming from each parent.
What is Homologous Pair?
Homologous refers to chromosomes that are similar in size, shape, and carry the same genes, with one chromosome coming from each parent.
What is genetic continuity?
Genetic continuity refers to the maintenance of the number and type of genes in daughter cells, inherited from the parent cell, ensuring that genetic information is preserved for the survival and functioning of the organism
Who is the father of genetics?
Gregor Mendel
What is Mendels first law?
States Allele pairs segregate randomly during gamete formation and unite during fertilization to form the genotype of the offspring.”
What is non-segregation?
This is when allele Pais are unable to separate during meiosis one which results in genetic disorder
State the law of Assortment
The Law of Independent Assortment states that genes for different traits are passed on independently of one another from parent to offspring during gamete formation. This process occurs during metaphase I of meiosis, where homologous chromosomes are randomly arranged and separated, ensuring that offspring receive a mix of chromosomes from both parents.
What is crossing over?
Crossing over is the process where non-sister chromatids of homologous chromosomes exchange genetic material at points called chiasma during prophase I of meiosis. This leads to new allele combinations and increases genetic variation in gametes.
What is the point known as where cross over takes place?
Chiasma