Yes they do just like we do
Explanation:
Meiosis makes genetic variety possible. It makes sperm & egg cells called gametes. Each gamete has 23 chromosomes. To make a diploid cell two gametes (sperm & cell) come together.
During prophase 1 the chromosomes pair up with their homologous pairs so they can transfer their genetic information and exchange it between each other. It makes recombinant chromosomes that influence the genetic diversity between the same people.
Now they are in metaphase 1, the chromosomes are in pairs in the middle of the cell. In anaphase 1, the chromosomes are pulled away by the spindle fibers. Then in telophase 1, there are two formed nuclei. Cytokinesis 1 then splits the cytoplasm.
Now they are in meiosis 2. During prophase 2, there are chromosomes and the spindles are starting to form again without crossing over like in prophase 1. In metaphase 2, chromosomes are going to line up in the middle in both cells unlike during metaphase 1 where the chromosomes were only in pairs. In anaphase 2, only the chromatids are being pulled away by the spindle fibers. Next in telophase 2 the nuclei reform and the 2 cells are each going to divide into 4 cells. Finally, cytokinesis completely splits the cytoplasm.
Keeping in mind that each sex only produces one type of gamete cell (sperm or eggs), and of the independent assortment and crossing over of chromosomes, the end result will be diversity.
Answer:
Yes, extra chromosomes can be received by the tasmanian devil.
Explanation:
Extra chromosomes can be received by the tasmanian devil due to tumor disease in the tasmanian devil. In the beginning the old genome of tasmanian devil has 13 chromosomes but with the tumor disease, it receives one extra chromosome and completed 14 chromosomes. Tumor occurs when the dead cells are not removed from the body and the new ones are formed.
A linear shaped piece of DNA strand is obtained when a plasmid is cut HindIII, Apa1, and Sma1.
Explanation:
Restriction enzymes are endonucleases which enzymatic proteins which can cut a DNA at specific sequences at particular recognition sites. The sequences recognized by these enzymes are usually palindromic that occurs for a definite length (6 bp, 4 bp, or 8 bp).
They can either be blunt cutters or sticky end cutters. APA1, SMA1, and HindIII are all restriction enzymes which can cut a circular plasmid at specific locations.
These restriction enzymes bind with the DNA at specific locations and cuts them to give linear strands of DNA either with a blunt or a sticky end.
