Let us solve first the
phenotype of this problem.
Starchy grain = AA (dominant)
Sugary Corn = aa (recessive)
AA x aa = AaAa ; AaAa
<span> A A</span>
<span>a Aa Aa</span>
<span>a Aa Aa</span>
The result of the cross is
that the progeny will become heterozygous.
<span>If there is 58 progeny
sugary, there will also be 58 starchy. It is 50%.</span>
Answer:
A mutation in <u>DNA </u>results in a change in <u>RNA </u>that sometimes produces a <u>protein </u>with altered structure and function.
Explanation:
DNA is the hereditary material which causes gene expression in our body by producing protein. The type of protein which is produced by DNA totally depends upon the sequence of nucleotides in the DNA. But, DNA molecule does not produce protein directly. Initially it produces RNA (mRNA, tRNA, rRNA) by the process of transcription, the nucleotides in the RNA are complimentary to those in DNA. In short, the message regarding the structure and composition of the type protein to be produced by DNA is first decoded from DNA in the form of RNA. These RNA molecules then synthesize the protein as per the instructions from DNA by the process of translation.
But, in case a mutation occurs in the DNA which causes a change in it's nucleotide/nucleotides, the protein which will be produced will be different in the structure and function than the protein which was supposed to be synthesized. It happens because, a triplet of nucletiodes in the DNA and hence RNA specifies a particular type of amino acid and several amino acids are joined in a long chain to form polypeptide which ultimately forms protein. But, if any nucleotide in the triplet is changed due to mutation it may change the amino acid and if amino acid will change the protein will also get altered.
It breaks apart the hydrogen bonds
C: primary Consumer
<em>primary consumers</em> are typically animals that eat plants aka herbivores.
<em>producers </em>would be plants
<em>secondary consumers </em>are typically ones that eat meat or eat meat and plants aka omnivores.
<em>decomposers, </em>I believe are like your fungus or anything that feeds off of dead organisms or eat the waste of that organism.
Hopefully this helped. I remember learning about this in college.
The pattern of inheritance of the offspring of a hemophiliac father would be heterozygous.
<h3>What is Hemophilia?</h3>
Hemophilia is defined as the sex–linked disorder that occurs due to an abnormality of the X chromosome.
A father that has hemophilia would be affected only on his X chromosome and can only pass it to their children making them carries.
This is because the children would inherit only one X chromosome from their father and a healthy X chromosome from their mother.
Learn more about chromosome here:
brainly.com/question/269366
#SPJ1
