Answer:
The options to this question are:
A) allele
B) codon
C) nucleotide
D) chromosome
The answer is A) allele
Explanation:
RNA and DNA are the two nucleic acids in living organisms used for transferring and storing genetic information. Deoxyribonucleic acid (DNA) is the genetic material in living organisms that contains segment coding for useful products/proteins and transmits genetic information from one generation to another. These segments are called GENES.
However, genes contain an alternate form responsible for genetic variation in the traits coded for by them. These alternate or variant form of a gene is called ALLELE. In a diploid organism like human, each trait is encoded by genes which contain contrasting pair of alleles that allows variation for that particular trait i.e. two alleles for each gene. For example, height trait in humans are encoded by gene, which possess two alleles; one coding for short variety (t) and the other for tall variety (T).
Answer:
12 : 3 : 1
white : yellow : green
Explanation:
Given that genes A and B control the fruit colour in following ways:
A_B_ or A_bb = white
aaB_ = yellow
aabb = green
The genes undergo independent assortment so:
AaBb X AaBb =
A_B_ : A_bb : aaB_ : aabb
9 : 3 : 3 : 1
white : white : yellow: green
12 : 3 : 1
Hence, ratio of white : yellow : green is 12: 3: 1
Answer:
genomic imprinting
Explanation:
Genomic imprinting is a mechanism for regulating gene expression that allows expression of only one of the parental alleles, although both alleles are functional. Unlike most genes in which expression is biallelic, genes that are subjected to this mechanism (imprinted genes) have monoalelic expression; By definition, in an imprinted loci, only one allele is active (maternal or paternal), and the inactive is epigenetically marked by histonic modification and / or methylation of cytosines.
Genomic imprinting can cause some disturbances, among them Prader-Willi syndrome, which is a genetic disorder that involves a partial deletion of chromosome 15q on the paternal chromosome.
Hereditary mutation - may be passed to another generation, occurs in gametes, variation that may enhance survival.
Somatic mutation - not passed from generation to generations, occurs in body cells.
Both- changes in DNA.
<h3><u>Explanation:</u></h3>
Mutations are defined as sudden changes in DNA that takes place by changing a particular nucleotide or a portion of DNA, or even a whole chromosome which has potential to change characters of an organism. Mutation was first proposed by Hugo de Vries who is also known as the Father of Mutation Theory.
Mutations can occur in any cell of body. It may occur in somatic cells, or in germ mother cells. But the mutations that occur in germ mother cells are actually the mutations that are carried forward by the gametes into next generations. Mutation in somatic cells get obliterated as the organism dies. And the Mutation in gamete cells are those mutations which are capable to cause variations in progenies which can led to better survival of the progenies.
