Answer:
The mRNA strands go to the cytoplasm to meet ribosomes so protein synthesis can start.
Explanation:
In protein synthesis, the first step is to <em>synthesize messenger RNA</em>, mRNA. The coping process of the DNA section for the desired protein is called <u><em>transcription</em></u>, and it happens in the <em>nucleus</em>. After that, it occurs <em><u>translation</u></em>, when the formed <em>mRNA moves to the </em><em>cytoplasm</em> through the nucleus membrane pores. Protein synthesis is initiated in the cytoplasm when mRNA meets a free ribosome, the primary structure for protein synthesis. Ribosomes are made of <em>protein and ribosomal RNA</em> and can be found in the r<em>ough endoplasmic reticulum</em> or floating in the <em>cytosol</em>. They read the mRNA code and add the correct amino acid using <em>transference RNA</em> to build the protein. mARN has a <em>start and end codon</em> that tells where to start and stop adding amino acids. When the ribosome reaches the end codon, it means that protein synthesis is finished. The new protein is driven to the rough endoplasmic reticulum and translocated to the lumen. Once there, the protein suffers a few modifications, one of them is <em>folding</em> to become functional. Finally, protein is transported by vesicles to the Golgi complex, and from there to its final destiny.
I think the enzyme photolyase is activated by light and can repair thymine dimers caused by UV radiation. Exposure to UV radiation is the main factor that causes skin cells to become cancer cells. These enzymes are involved in the repair of ultraviolet light-induced DNA damage when activated by light absorption.
C i think...................
Answer:
Increasing substrate concentration
Explanation:
i just took a test for this
