Additional information is missing. It is as follows: In fruit flies, the allele for red eyes is dominant over the allele for pink eyes. Straight wings are dominant over curled wings.
Answer:
Genotype = RrSS and RrSs in 1:1 ratio so each has 0.5 probability
Phenotype = All red eyed and straight winged
Explanation:
Given,
Red eyes (R) is dominant over pink eyes (r)
Straight wings (S) is dominant over curled wings (s)
Fly 1 : Homozygous red eyed, curly winged = RRss
Fly 2 : Pink eyed, heterozygous straight winged = rrSs
RRss will produce Rs gametes and rrSs will produce rS and rs gamates.
When fly 1 and fly 2 mate : RRss X rrSs :
rS rs
RS RrSS RrSs
The genotypic ratio is 1 : 1 ( RrSS : RrSs ) that means that each genotype has 0.5 probability. Both the genotypes though have at least one dominant allele for each gene so the entire progeny will have red eyes and straight wings.
Answer:
Thymine
Explanation:
Adenine is a Purines together with Guanine .
Purines always pair with Pyrimidines ; which are cyosine and Thymine.
This is a complementary base pairing that hold the two strands of DNA bases together by weak hydrogen bonds for flexibility and easily unwind during replication
Purines are larger in size beaxuae they have 2 ring structures while Pyrimidines aee smaller because of one ring structure.
Therefore two purines (Adenine and Guanine can not pair together;
It must be a Purines -Pyrimidines pairs.
Therefore Adenine must pair with Thymine and cyosine with Guanine
In RNA, Thymine are replaced with URACIL as Pyrimidines.
.
Carolus Linnaeus developed a two-word naming system called binomial nomenclature. in binomial nomenclature, each species is assigned a two-part scientific name.
Hope this helps :))
Answer:
You use the control group against an experimental group to see if there is a change when you add a variable. Th control group is the group without the variable you are testing.
Correct answer: D). Deletion
Tay-Sachs disease is an autosomal hereditary disease that is known to affect the central nervous system. It results from the mutation caused in the gene that encodes for the beta-hexosaminidase enzyme. It is a lysosomal enzyme that is composed of the beta and alpha polypeptides.
It is caused when both the parents are a carrier, it occurs when a baby is born in absence of hexosaminidase. It affects the nervous system and can change the physical appearance after a few months of the birth.
