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Flura [38]
3 years ago
9

If hardy-weinberg conditions exist, what will happen to the frequency of a dominant allele over time? the frequency will increas

e. the frequency will decrease. the frequency will remain the same. the frequency will double with each generation. it is impossible to predict the frequency.
Biology
2 answers:
8090 [49]3 years ago
5 0

Answer:

its frequency will remain the same

Explanation:

Darya [45]3 years ago
3 0

its frequency will remain the same

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You take a human smooth muscle cell and block the release of calcium from the sarcoplasmic reticulum. What effect does that have
Murljashka [212]

Answer:

The correct option is E) Contraction still occurs because Ca2+ can enter the cell directly through Ca2+ channels in the plasma membrane and bind to calmodulin.

Usually, the calcium ions are released from the sarcoplasmic reticulum of a cell during a muscle contraction, but if those are blocked, the contractions is an cell can still arise through the calcium ions which are present in the cell membrane of a cell.

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3 0
4 years ago
If thymidine dimers created by UV irradiation persist until DNA replication, DNA polymerase is likely to make a mistake reading
marishachu [46]

Answer:

Thymidine dimers is likely to be repair as soon as it is originated but if left unrepaired then it causes  frame shift mutations.

Explanation:

In case of Bacterium if UV irradiation induces covalent linkage of two thymidine present adjacently to each other or on a single strand to make thymidine dimers.

These either excised via DNA repair enzyme like Endonuclease V and the proof reading activity of DNA polymerase I enzyme help in incorporation of nucleotide by taking the unmutated original strand as a template.

These dimers if not excised before second round of replication than the sequence of newly synthesized strand will be altered. As DNA polymerase III enzyme read thymidine dimers as single thymidine nucleotide and incorporate only 1 adenine in the newly synthesizing complementary strand which results in frame shift mutations

It is the mutation in which reading frame of codons is shifted or altered due to deletion or addition of a single nucleotide.

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