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KengaRu [80]
2 years ago
9

In Drosophila, the genes crossveinless-c and Stubble are linked, about 7 map units apart on chromosome 3. cv-c is a recessive mu

tant allele of crossveinless-c (cv-c+ is wild type), while Sb is a dominant mutant allele of Stubble (Sb+ is wild type). A dihybrid female Drosophila with genotype cv-c Sb+/cv-c+Sb is testcrossed. The proportion of phenotypically wild-type individuals in the progeny of the testcross will be:
Biology
1 answer:
Sav [38]2 years ago
7 0

Answer:

3.5%

Explanation:

The genes crossveinless and Stubble are linked and 7mu apart. That means that the frequency of recombination between them during meiosis will be 7%.

The alleles for crossveinless are:

  • cv-c+ wildtype, dominant
  • cv-c mutation, recessive

The alleles for Stubble are:

  • Sb mutant, dominant
  • Sb+ wildtype, recessive

A dihybrid female Drosophila with genotype cv-c Sb+/cv-c+Sb is testcrossed (crossed with a homozygous recessive male):

cv-c Sb+/cv-c+Sb X  cv-c Sb+/ cv-c Sb+

<u>The male can only produce one type of gametes:</u> cv-c Sb+

<u>The female can produce 4 types of gametes:</u>

  • cv-c Sb+ Parental, 46.5%
  • cv-c+Sb Parental, 46.5%
  • cv-c Sb Recombinant, 3.5%
  • cv-c+Sb+ Recombinant, 3.5%

The frequency of recombination between cv-c and Sb is 7%, and 2 recombinant gametes are formed, so each of them will appear 3.5% of the times. The parental gametes will have a frequency of 100%-7%=93%, and there are 2 of them so each will have a frequency of 46.5%.

Only when the recombinant gamete cv-c+Sb+ joins the gamete generated by the male parent will the offspring be wild-type for both genes, so the proportion of phenotypically wild-type individuals in the progeny will be 3.5%.

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The process of protein denaturation Multiple Choice: a) is only possible in proteins with quaternary structure. b) is permanent
pav-90 [236]

Answer:

The correct option is D.

Explanation:

Protein generally are very sensitive macro molecules; they have specific temperatures and pH that are ideal for their operations, this is especially true for proteins that act as enzymes in biochemical reactions.

There are four different types of structures that a protein can assume, these are primary, secondary, tertiary and Quaternary structure. The structure of a protein determines the kind of function it can perform.

There are some factors that can destroy the structure and functions of proteins, these include excessive heat and pH. A protein is said to be denatured when its secondary and tertiary structure have been disrupted or destroyed. Denaturation does not affect the primary structure of the protein, thus, the peptide bond remains intact.

Denaturation is usually temporary and can be reversed if the factors that cause denaturation is removed, this process is called RENATURATION. Renaturation process allow the protein to refold and resume its functions.  But sometimes,  denaturation  can be permanent and irreversible leading to permanent loss of protein functions.

7 0
2 years ago
The strand of dna used in the previous problem undergoes a mutation, such that the second c from the 3' end is changed to a
dlinn [17]
This mutation type is a substitution mutation. Substitution mutations may be silent or may have adverse effects (missense mutation).
Adverse effects come about because the change in codons in mRNA transcribed from the DNA strand. A point substitution can change the amino acid being coded for in the particular polypeptide change. If that animo acid is a structural residue of the protein, the structure of the protein will be altered, which may or may not lead to a change in protein function. If that particular amino acid is a catalytic residue of the protein, it may alter the 3D conformation and charge of the active site (if protein is an enzyme) or the binding site of protein. Function of protein formed from mutated DNA will be lost or altered.

Hope this helps! :)
6 0
2 years ago
The state of health and functioning of the liver is often assessed with dye-tracer techniques. The dye used most frequently is b
elena-s [515]

Answer

1.Radioactive or chemical decay

2. X(t) = Xoe^-kt

lnY(t) = -t + lnYo

4. 6.07mg

Explanation:

Let the liver and and blood compartment be represented by the symbol L and B respectively

For the liver

Suppose a first Order removal process started with an amount X, in which amount b disappeared in time t, the process is decay process which can be represented as follows,

∫dX/dt = -K1X

By rearrangement and integration;

∫dX/X = -K1t

ln X = -K1t + C

Since At t= 0, X = Xo then

C = lnXo

The equation becomes:

lnX = -K1t + lnXo

lnX - lnXo = -K1t

ln(X/Xo) = -K1t

X/Xo = e^-kt

X(t) = Xoe^-kt

X(t) = Xoe^-0.5t........(2)

Similarly for B (blood), suppose a first order flow flow of the dye move from the blood to the liver, let Y be the initial concentration, and amount b that has flown to the liver in time t

B---------> B(t)

t=0 Yo 0

t=t. Y-b. b

dY/dt = -K12(Y-b)...........(3)

Let Y-b = Y(t)

∫dY/dt = -∫K12t

By rearrangement and integration;

∫dy/Y(t) = ∫-K12dt

lnY(t) = -K12t + C1

at t= 0, C1 = ln(Yo)

Therefore ln Y(t) = -K12t + lnYo

But K12 =1

ln Y(t) = -t + lnYo.............(4)

(3) The assumptions used here

is that of a decay for the liver . The amount remaining taking as the amount of a substance

(4) using the equation 2,

X(t)= Xo e^-K1t........(2)

For time t = 1hour, and an initial amount X = 10mg, K = 0.5

X(t) = 10× e^-0.5

X(t) = 10 × 0.607

X(t) = 6.07mg

(5) within the scope of information presented, I have no data to make this judgment.

3 0
2 years ago
Historically, the x chromosome had more genes assigned to it than its physical size would seem to warrant relative to the other
sweet-ann [11.9K]

Answer:

Humans contain 46 chromosome or 23 pairs of chromosomes. Among them  22 pairs are autosomes and one pair contains the sex chromosome. Humans female are XX and human males are XY.

The X chromosome determines the sex of an individual and females one X chromosome is randomly inactivated. The human X chromosome has large number of genes and contains large euchromatic regions that are highly activating gene regions. The X chromosome also contains the conserved regions that are far shorter in Y chromosome. The X chromosome is large in size and has large number of genes.

5 0
2 years ago
Why does the mouthpiece of an aphid contains a high concentration of dissolved sugars after feeding
Korolek [52]
An aphid eats from grass which creates High levels of glucose from the process of photosynthesis therefore when the aphid eats the grass the glucose is transferred to the aphid and as a result has a higher concentration of dissolved sugars
6 0
2 years ago
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