Answer:
1. 50% of the genome comes from each parent because it is crucial otherwise if the ratio changes, the zygote may not form and if formed the fetus may have some other kind of chromosome number related syndromes etc.
2. Sexual reproduction produces greater genetic variability than asexual methods. This is because of the process of crossing over during meiosis that exchange the segments of chromosome that is necessary for producing mutations and genetic variability.
3. 50% of chromosomes match with each parent because both of the parents contributed 23 chromosomes and exactly 50% of their genome.
4. The gametes must be produced by two different individuals cause that is the main purpose of sexual reproduction and give better survival like this to the forming next generation. Not to mention produces greater genetic variability among species.
5. Plants always produces both eggs because they are hermaphroditic in nature.
Answer:
<em>The correct option is D) cytokinesis</em>
Explanation:
Mitosis can be described as a process in a cell replicates to form two identical copies of itself.
Cytokinesis can be described as the last stage of cell division for both prokaryotes and eukaryotes. During this stage, the cytoplasm eventually divides and the cell splits into two with equal portions of cytoplasm in each side. Although the mechanism of cytokinesis is different for both plants and animals yet it is the final stage for both the cell type in which the cytoplasm splits.
Established on the data, sickle cell hemoglobin displays altered primary structure and altered quaternary structure; the secondary and tertiary structures may or may not be altered. The sickle cell disease is a cluster of disorders that disturbs hemoglobin, the molecule in red blood cells that transports oxygen to cells all over the body. A person with this disorder have uncharacteristic hemoglobin molecules named hemoglobin S which can interfere with red blood cells into a sickle or crescent shape.
Answer:
to break down food
Explanation:
and also to absorb nutrients
In chromatin, substitution mutations are most common in linker regions. Option d is the correct answer.
Mutation by substitution When one nucleotide base is replaced by another, this occurs. Mismatch mutation A type of substitution mutation in which a single nucleotide is replaced, resulting in the coding of an incorrect amino acid, which usually results in a malfunctioning protein. Silent mutations are the result of genetic code redundancy (degeneracy): This is false, as silent mutations are the result of a base substitution that has no discernible effect on a protein's amino acid sequence.
Learn motre more about subsitution here:
brainly.com/question/29383142
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