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hoa [83]
2 years ago
9

A scientist discovers a cell that has chloroplasts, cytoplasm, DNA, and a cell membrane. Which statement best describes how the

cell could be classified? The cell is prokaryotic because it has DNA. The cell is prokaryotic because it has cytoplasm. The cell is eukaryotic because it has a cell membrane. The cell is eukaryotic because it has chloroplasts.
Biology
2 answers:
Zina [86]2 years ago
4 0
<span>The correct answer is The cell is eukaryotic because it has chloroplasts. Prokaryotic cells don't have chloroplasts as they are only found in eukaryotic cells. The closest thing there is to chloroplasts are the cyanobacteria who function similarly and also photosynthesize but are in the end not chloroplasts themselves.</span>
weqwewe [10]2 years ago
4 0

D. The cell is eukaryotic because it has chloroplasts.

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Galactosemia is a metabolic disorder characterized by the inability to metabolize the sugar galactose. People with galactosemia
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Answer:

Genetic mapping for unequivocal identification of the potentially causative mutation  

Explanation:

Galactosemia is a genetic disorder caused by mutations in the Galactose-1-phosphate uridylyltransferase (GALT) gene, which encodes an enzyme involved in the metabolism of galactose. Gene mapping is a technique widely used in genetics to identify the position of one locus a chromosome by using molecular markers to estimate genetic distances. Genetic mapping provides useful evidence in order to identify when a disease that is transmitted from parent to offspring can be associated with one or more genes and then determine which gene/s is/are responsible for this condition.

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3.How many plants were likely to have been in the<br> pond on day 15?
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Rosa drew a diagram to compare substitution mutations and insertion mutations.
djverab [1.8K]
<h2>Hey There!</h2><h2>_____________________________________</h2><h2>Answer:</h2>

\huge\boxed{Option A}

<h2>_____________________________________</h2><h2>Mutations:</h2>

Mutations are the changes produced in the nucleotide sequence of the genome.

There are four main types of mutations

Substitution

Insertion

Deletion

Duplication.

<h2>_____________________________________</h2><h3>DELETION:</h3>

A small segment of chromosome mat be missing. This condition is known as deletion.

For example, Normal chromosome has A B C D E F G. If deletion mutation occurs then mutated chromosome has A D E F G and B C got deleted.

<h2>_____________________________________</h2><h3>DUPLICATION:</h3>

In this condition, a part of chromosome present in exec ess to the normal chromosome.

For example, Normal Chromosome has A B C D E F G. If duplication mutation occurs, then mutated chromosome had A B C B C D E F G and B C is duplicated.

<h2>_____________________________________</h2><h3>SUBSTITUTION MUTATION:</h3>

Substitution is a type of mutation where one base pair is replaced by a different base pair.

For example, in the sequence CAAGT, if C replaces G, it is a substitution mutation.

<h3>INSERTION MUTATION:</h3>

In genetics, an insertion is the addition of one or more nucleotide base pairs into a DNA sequence.

For example, in the sequence CAAGT, if extra base G gets inserted after C, the new sequence would be CGAAGT.

<h2>_____________________________________</h2>

Both substitution and insertion mutations change the position of nucleotide thus, the type of amino acid.

<h2>_____________________________________</h2><h2>Best Regards,</h2><h2>'Borz'</h2>

3 0
1 year ago
Read 2 more answers
Jill is heterozygous for gene A and is going to have a child with Jack, who is homozygous recessive for gene A. Which of the fol
Igoryamba

Answer:

D. Aa

Explanation:

Given:

Jill (mother) is heterozygous for gene A --------- i.e Jill = Aa

Jack (father) who is homozygous recessive for gene A-------- i.e Jack = aa

Now if both cross and fertilization occurs, we have:

         A          a

a        Aa        aa

a        Aa        aa

The offsprings are (Aa, Aa, aa, aa)

Nondsijunction is the inability of homologous chromosomes to seperate properly during cell division. Now, we were told that this fertilization undergone nondisjunction in meiosis 1. Hence, both homologous chromosome move into the same daughter cells instead of different daughter cells because separation of homologous chromosome does not occur properly.

Therefore the result of these fertilization of a normal haploid sperm with an egg that had undergone nondisjunction in meiosis yields offspring with genotype Aa of their Mother (Jill).

4 0
2 years ago
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