Answer
- causes genetic recombination
- causes genetic variation
Explanation;
-Meiosis is a type of cell division which in which cells involved divides into four daughter cells which have half the number of chromosomes as the parent cells.
-Meiosis is important as it results to genetic variation in organisms through the process of cross over, in which genetic materials are exchanged by the homologous chromosomes, where segments of chromosome are exchanged by non-sister chromatids.
-Additionally, meiosis results to genetic recombination as a result of pairing of homologous chromosomes. This takes place when two molecules of DNA exchange their genetic material with one other.
Complex carbohydrates
Such as insoluble fiber. Your body will break that down first because I is much faster than other source to convert to energy. If there isn't any carbs available your body will then convert fat into energy and lastly if there is t and carbs or fat your body will then breakdown protien into energy but that is truly the last resort. Sorry for the errors in this texts I was writing very fast and my phone will not allow me to edit.
If signals stop working properly, then cell division may occur rapidly or not occur at all. This can cause cancer or infections due to a lack of wound healing.
I hope I helpedb
Answer:
Generate moral statements.
Explanation:
The scientific methods may be defined as the empirical methods that are used to characterize the development of science. The assumptions can be explained on the scientific levels.
Scientific methods involves the different strategy and procedures to explain the particular phenomena of the nature. The moral statements cannot be generated by the scientific methods and can only believes on the scientific evidence.
Thus, the correct answer is option (c).
Answer:
C) An extra chromosome is added, causing mismatching of the chromosome pairs.
Explanation:
Mutation is any change, whether big or small, that occurs in the nucleotide sequence of a gene. Mutation can be of different types depending on how it occurs.
According to the question, frameshift mutation is a mutation that causes the normal reading frame of the nucleotide sequence to be altered. It is caused when an extra chromosome is added (insertion) or when one chromosome is removed (deletion). In either way, there will be a mismatch or alteration in the chromosome pair, hence affecting the reading of the nucleotide sequence.
In frameshift mutation, the insertion or deletion causes the
normal CODONS (triplet nucleotide) to be missing or incomplete, hence, disrupts the manner at which the reading takes place (reading frame). Note, frameshift mutation only occurs as a result of insertion or deletion of chromosomes/bases that are not multiples of three that can maintain the normal reading pattern/frame.
