Answer:
DNA replication a process of copying of a cell's DNA. DNA replication is semiconservative process which means that each strand in the double helix helps in the synthesis of new, complementary strand and conserve the parent template.
The Molecular mechanism of DNA replication is as following:
- The double starnded DN in binded with hydrogen bond, the enzyme helicase opens up the DNA at the replication fork.
- A single stranded binding protein prevent the rewinding of DNA and so binds to the DNA around the replication fork
- Topoisomerase prevent supercoiling at replication fork.
- The ezymes primase come in action and produces RNA primers which are complementary to the DNA strand.
- DNA polymerase III help to extends the primers and allow them to add to the 3' end, to make new DNA.
- DNA Polymerase then remove RNA primers and replace with DNA.
- DNA ligase blocks the the gaps between DNA fragments.
So, this is the molecuar mechanism of DNA replication.
Answer:
guanine, adenine, cytosine,
Explanation:
Answer:
c. autotrophs and animals are heterotrophs
Explanation:
There's many differences between the plants and the animals, be it their physical appearance, way of live, how do they function, their requirements for survival. One of the major differences between the plants and the animals is that the plants are autrotrophs, while the animals are heterotrophs. The autrophs are the organisms that are able to produce their own food, thus they are producers, meaning that they do not need nutrition from other organic sources. The heterotrophs on the other side are the organisms that are not able to produce food for themselves, but instead they get their food through consuming of other living organisms, making them primary, secondary, and tertiary consumers.
Explanation:
<u>C. A red allele is present on both homologous chromosomes</u>
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Homologous chromosomes are pairs of chromosome of similar lengths, banding patterns, and centromere positions, with genes at the same loci. For dominance, gene copies are present on both of the chromosomes; the dominat variant overrides the effect of the other recessive allele.
Further Explanation:
DNA molecules contain chromosomes that may have different forms called alleles. DNA, which is the genotype, is transcribed into mRNA and later translated into amino acids which are connected together by rRNA to form proteins which constitute the phenotype of an organism. DNA sequence mutations form new alleles, impacting the associated mRNA, and thus the encoded protein.
Homozygous individuals have a chromosome containing two variants of the same allele. Dominant homozygous individuals bear two copies of the dominant allele, whereas recessive homozygous individuals hold two copies of the recessive allele.
Learn more about mutations at brainly.com/question/4602376
Learn more about DNA and RNA at brainly.com/question/2416343?source=aid8411316
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