Answer:A. The release of calcium ions causes myosin and actin to attach to each other.
The contraction of skeletal muscles takes place by induction of a nerve impulse, which produces a movement and the interaction of the filaments containing proteins named as actin and myosin. This interaction of filaments is regulated by proteins called tropomyosin and troponin present on the actin filaments. The motor nerve causes the depolarization of the muscle membrane sarcolemma. This triggers the sarcoplasmic reticulum to release calcium ions. This calcium binds to troponin and thus allows the tropomyosine strand on the actin filament to displace so that the part of the actin where myosine head needs to be attached remain uncovered. Binding of the actin myosine filament results in contraction.
Hence, the release of calcium ions causes myosin and actin to attach to each other causes muscle contraction.
Honestly it would be the Exosphere<span> but since that's not one of the choices it would be the Thermosphere. </span>
A
Explanation:
The genome of prokaryotes has no introns hence their mRNA does not need splicing like in eukaryotic cells. Also, because the genome of prokaryotes is not delimited from the cytoplasm by a nuclear membrane, ribosomes can attach to the elongating mRNA during transcription and begin translation. Therefore translation of mRNA occurs concurrently with transcription which cannot happen with eukaryotic cells.
In the nucleus of eukaryotic cells, transcription results to a nascent mRNA which is spliced into a mature mRNA.The mature mRNA has to travel outside the nucleus to the cytoplasm to be translated by ribosomes.
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B. Mutations cause a person's body cells to divide uncontrollably. There isn't a signal for cells to stop dividing, so this can cause cancer because cancer cells won't stop dividing without this signal.
Answer:
1. The difference between the normal hemoglobin protein DNA sequence and the sickle cell hemoglobin DNA sequence is a base to base shift, in this case adenine (GAG) to thymine (GTG).
2. The difference affects the amino acid sequence of the protein by replacing glutamic acid (Glu) with valine (Val).
Explanation:
In sickle cell anemia, a change in the DNA nucleotide sequence is observed, where adenine is substituted by thymine, whose expression is the change in the amino acid sequence of globine β, incorporating valine instead of glutamic acid. This represents a molecular mutation - point mutation - by subtitution, which corresponds to missense mutation.
<u>Normal hemoglobin protein in a RBC</u>
DNA CTG ACT CCT GAG GAG AAG TCT
Amino acids Leu Thr Pro Glu Glu Lys Ser
<u>Sickle cell hemoglobin protein in a RBC</u>
DNA CTG ACT CCT <em>GTG</em> GAG AAG TCT
Amino acids Leu Thr Pro <em>Val</em> Glu Lys Ser
When GAG is transcribed to mRNA, the CUC codon is obtained, which codes for glutamic acid. Thymine substitution causes the DNA sequence to change to GTG, which is transcribed as CAC, the codon that encodes the amino acid valine. The <u>change from glutamic acid to valine in β-globin causes an altered hemoglobin, giving the abnormal erythrocytes observed in sickle cell disease</u>.
