Answer:
Malignant melanoma cells would have active telomerases that constantly replenish and lengthen telomeres.
Explanation:
Telomerase can be described as enzymes which add the repetitive sequences called telomeres at the end of a chromosome. Telomeres can be described as repetitive sequences at the end of the chromosome which are involved in protecting the chromosome from any damage.
In a normal skin cell, the telomeres will shorten with time. But in a malignant skin cell, the telomerase will add the repetitive sequence again and again. The telomers will not be able to shorten.
The fossils from
Australopithecus provide evidence for evolution because some parts of the bone
that contains the DNA of it can be identified as this type of animal. They can
be detected through the use of carbon dating devices.
Answer:
A molecule of mRNA is formed.
Explanation:
Translation is the second process that occurs in gene expression. It is the process by which the information encoded in the mRNA transcript is used to synthesize a protein.
The mRNA nucleotide sequence is read in a group of three nucleotides called CODON. Each codon specifies an amino acid. Translation, which occurs in the ribosomes (cytoplasm), reads the codon with an anticodon using the complementary base pairing rule i.e. A-U, G-C. This means that a CODON-ANTICODON pairs.
The anticodon carries a corresponding amino acid to the polypeptide sequence. A peptide bond is formed when two amino acids joins together in a condensation reaction.
Note: A molecule of mRNA is formed during transcription
Answer:
the reporter gene can randomly insert near to an enhancer sequence which can induce its expression
Explanation
Enhancers are genetic sequences capable of activating gene expression by binding to specific proteins (e.g., transcription factors). Enhancers can regulate the expression of nearby genes located thousands of nucleotides away, i.e., over several kilobases away. In the human genome, it is well known that enhancers are scattered across the 98% of the genome. In this case, it is expected that the reporter GFP gene construct is randomly inserted near an enhancer sequence (a 10% chance of insertion), thereby being regulated by that enhancer.
Answer:
There will be few if any complications.
Explanation:
Just took the unit test review
