Answer:
Some diseases are more common in certain groups of people, such as Caucasians or African Americans because individuals in such ethnic groups often share certain alleles (versions of their genes), that have been passed down to them from common ancestors and a particular genetic disorder may be more frequently seen in such groups if one of these shared genes contains a disease-causing mutation.
Explanation:
Some genetic diseases are frequently seen in certain ethnic groups like Caucasians or African Americans. Individuals in such groups often share certain alleles (versions of their genes), that have been passed down to them from common ancestors and one of these shared genes may contains a disease-causing mutation.
Examples of certain genetic disorders that are more common in particular ethnic groups include the Tay-Sachs disease, which is more common in people of eastern and central Europe (Ashkenazi), Jewish or French Canadian ancestry and the sickle cell disease, which occur among people of African, African American, or Mediterranean heritage.
Some genetic disorders are more common in people whose ancestry can be traced to a particular geographic area. The factors that can lead to development of populations with very different genetic allele frequencies include their geographic origin, selection, patterns of migration, historic events, etc. Certain natural barriers like oceans and other water bodies, high mountains, large deserts, or major cultural factors had prevented communication and interaction between people. So mating was restricted within the group, and this produces genetic marker differences and differences in the presence of specific disease-related alleles.
Answer:
As they produce food by the process of photosynthesis which cannot be done by anyone else. Plants use chlorophyll, CO2 and H2O in photosynthesis( which is a biochemical process). Plants became a cause of life on earth. Hence plants are the ultimate source of food on earth.
Answer:
The correct answer would be C. The protein synthesized will contain many erroneous amino acids since the loss of one base will shift the reading of the encoded base sequence.
Deletion mutation that does not occur in the multiple of three bases can results in frame-shift mutation.
It changes the reading frame of nucleotide in DNA. Thus, the reading frame of codons in mRNA would also change.
Consequently, the sequence of amino acids in a polypeptide chain would change or alter. Thus, a protein would contain many erroneous amino acids.
An example of the same is shown below in the image.
A- valve replacement
b- stents
x- heart transplant
