Answer:
the last answer
Explanation:
because f,g,h both come from a so you can be sure
Answer:
1. Chromatin condense into chromosomes.
4. Homologous chromosomes pair up (formation of tetrads).
5. Homologous chromosomes separate and move to poles.
2. Sister chromatids separate.
3. Chromosomes unravel in to chromatin.
Explanation:
This question portrays the process of meiosis in a cell. The ordered sequence of events in the options are:
1. Chromatin condense into chromosomes - This process occurs in the Prophase stage. Prior to the cell division, the nuclear material is found as Chromatin material. This Chromatin material then undergoes condensation to form visible chromosomes.
4. Homologous chromosomes pair up (formation of tetrads) - This process also occurs during the Prophase stage of meiosis I. In this stage, homologous chromosomes (similar but non-identical chromosomes received from each parent) are paired up side by side to form a structure known as TETRAD or BIVALENT.
5. Homologous chromosomes separate and move to poles - This process characterizes the Anaphase stage of meiosis I. Homologous chromosomes are pulled apart to opposite poles of the cell by spindle microtubules.
2. Sister chromatids separate - After meiosis I, meiosis II involving sister chromatids instead of homologous chromosomes follows. In the Anaphase stage of meiosis II specifically, sister chromatids are pulled apart towards opposite poles of the cell.
3. Chromosomes unravel in to chromatin - After the whole division process i.e. karyokinesis (division of the nuclear material), the chromosomes begin to unravel to form the CHROMATIN threads once again. This process occurs in the Telophase stage of meiosis.
Answer:
Base substitution mutation
Explanation:
Mutation is the alteration or change that occurs to the sequence of a gene caused by a mutagen (chemicals) or spontaneously-induced. Depending on how the mutation occurs, it is of different types. The mutation shown in this question is as follows:
ATCGGCTTAACG to ATCGGCTAAACG
This type of mutation is called SUBSTITUTION MUTATION. Substitution mutation is a type of mutation that involves the replacement of one or more nucleotide base by another. In this original sequence; ATCGGCTTAACG, the eight base T was replaced by base A in the sequence, hence, it is a substitution mutation.
