Ok, so I wrote these out just to make it a little bit easier for you to understand what I am about to explain.
So for the first one you have two different traits that can be inherited- having freckles or having no freckles, F and f respectively. The dominant trait (or having freckles) is shown by the capital F, and is almost always expressed over the recessive trait, or the lowercase f. So, for example, if you have a genotype of Ff, the trait having freckles will show up instead of not having freckles. The only way that you could have the trait of no freckles show up is if there are two recessive alleles for having no freckles, or ff. In this case, you have two parents who are both heterozygous for the trait of having freckles, so in other words the mother has Ff and the father has Ff. Each parent passes down one allele to the offspring, so since you are breeding Ff and Ff, you should result in having the possible genotypes of FF, Ff, Ff, and ff. This means that there is a 25% chance that the offspring will be homozygous for having freckles, a 50% chance that the offspring will be heterozygous for having freckles and a 25% chance that they would be homozygous for having no freckles, or a 1:2:1 ratio.
Incomplete dominance is a little bit different that just a normal monohybrid cross. Instead of just the dominant gene showing up in a heterozygous genotype, both traits show up. So like the question says, if a homozygous red flower plant was crossed with a homozygous white flower plant, their offspring would not just be white or red, they would be pink because it is a mixture of white and red. So then if you crossed the heterozygous, or Rr plants, the result would be a 25% chance of getting a homozygous RR red plant, a 50% chance of getting a pink Rr plant, and a 25% chance of getting a white rr plant, or another 1:2:1 ratio.
Sorry for the wordy answer, but hopefully this helps you understand this a little better :)
D.) Both are circumstantial evidence....
Answer:
All of the above are true
Explanation:
Organisms possess two types of genome viz; prokaryotic genome and eukaryotic genome. The eukaryotic genome is possessed by cells with a well-defined nucleus, where their genetic material (DNA). The prokaryotic genome, on the other hand, lacks a membrane-bound nucleus. The major organization or content between these two genomes are:
- Prokaryotic genomes generally have less DNA and fewer genes than eukaryotic genomes.
- Prokaryotic genomes have fewer repeated sequences and noncoding, intragenic sequences than eukaryotic genomes.
- Most prokaryotic genomes are contained in one circular chromosome while most eukaryotic genomes are contained on several linear chromosomes.
- In general, eukaryotic genomes contain many introns, repeated sequences, and transposable elements.
Based on this, all of the above options are TRUE
Answer:
1.
mRNA - Messenger RNA: Encodes amino acid sequence of a polypeptide.
tRNA - Transfer RNA: Brings amino acids to ribosomes during translation.
rRNA - Ribosomal RNA: With ribosomal proteins, makes up the ribosomes, the organelles that translate the mRNA.
2.
Transcription is the process by which DNA is copied (transcribed) to mRNA, which carries the information needed for protein synthesis. Transcription takes place in two broad steps. First, pre-messenger RNA is formed, with the involvement of RNA polymerase enzymes.
3.
During translation, which is the second major step in gene expression, the mRNA is "read" according to the genetic code, which relates the DNA sequence to the amino acid sequence in proteins. Each group of three bases in mRNA constitutes a codon, and each codon specifies a particular amino acid (hence, it is a triplet code). The mRNA sequence is thus used as a template to assemble—in order—the chain of amino acids that form a protein.
Explanation: