Im pretty sure its plants
Answer:
The correct answer is: b. Budding of the secretory granule.
Explanation:
- In eukaryotic cells, the pathway by which secretory proteins are produced and are secreted can be explained below:
- The gene {DNA (Deoxyribonucleic Acid) sequence}, located on the genome, encoding the secretory protein is transcribed into an mRNA (messenger Ribonucleic Acid) by the RNA polymerase. This process happens in the Nucleus.
- The mature mRNA is translocated from the nucleus into the cytoplasm.
- In the cytoplasm it associates with the ribosome but translation process does not begin now.
- This is because, as the mRNA sequence has the tag of forming a secretory protein, it can be translated only when the ribosome bound mRNA sequence attaches itself to the ER (Endoplasmic Reticulum).
- On attachment to the ER, the process of translation begins and the polypeptide formed is released into the lumen of the ER.
- The process of glycosylation starts in the ER.
- The glycosylated protein is then transported from the ER in membrane bound vesicles to the cis, medial and trans Golgi, where the process of glycosylation gets completed and the protein gets completely folded.
- After this, secretory vesicles buds off from the Golgi and migrate towards the plasma membrane.
- At the plasma membrane, the secretory vesicles fuse with the plasma membrane and releases the protein out of the cell by the process of Exocytosis.
- In the given question completely folded glycosylated protein is formed but it is not secreted. This means the protein is able to reach to the Golgi bodies. But secretory vesicle formation does not take place.
- Hence the Substance X might inhibit the formation or budding of Secretory Vesicles.
When the two strands split
Answer:
1. A mutation that causes changes in the amino acid sequence downstream of the mutation is called FRAME SHIFT MUTATION. The correct option is D. A frame shift mutation is one in which the mutation is caused either by the addition or deletion of base pairs in the DNA of a gene, this results in the translation of the genetic code in the wrong reading frame starting from the position of the mutation to the end of the affected gene. Frame shift mutation result in the production of nucleotide that are not divisible by three. Because the nucleotide codons are usually pair in three, frame shift mutation causes a change in the reading frame and this result in a protein translation that is different from the original.
2. The correct option is D.
If the third base A is deleted from the codon given in the question, it will results in the formation of frame shift mutation and this will change the translation of the protein from leucine to tyrosine. The deletion will not affect the first amino acid in the sequence.
3. Albinism is a type of mutation that can is described as DELETERIOUS. The correct option is D.
Deleterious mutation refers to any type of mutation which reduces the fitness of a living organism. Albinism is a medical condition in which an individual experience a partial or total loss of skin pigmentation. The condition is a genetic disorder that is caused by lack of adequate amount of melanin pigment in the skin. Albinism causes vision loss, extreme sun sensitivity and stigma.
4. The type of mutation that occur is INSERTION. The correct option is B. Insertion is a type of mutation in which one or more nucleotide base pairs are added to a DNA sequence. The inserted base pairs can be small or large. Examples of disease conditions that resulted from insertion mutation are Huntington's disease and fragile X syndrome.
