Answer:
RNA molecules are made of nucleotides. (Ans. C)
Explanation:
RNA, which is also known as ribonucleic acid is found in cytoplasm of the cell, and synthesized in the nucleus. It is shorter, and a single stranded molecule. It is composed of one or more nucleotides which are linked together by phosphodiester bonds.
In RNA, the ribonucleotide contains pentose sugar ribose, four nitrogenous bases (A,U,C,G), and a phosphate group. RNA plays many types of role in cells, but mainly involved in the translation process, and it's regulation which is known as protein synthesis.
heir function is to base pair with the codon on a strand of mRNA during translation. This action ensures that the correct amino acid will be added to the growing polypeptide chain. A tRNA molecule will enter the ribosome bound to an amino acid.
Answer:
No hablo español, así que pido disculpas por cualquier error.
La teoría de la panspermia, que sugiere que la vida en la Tierra no se originó en nuestro planeta, sino que fue transportada aquí desde otro lugar del universo.
As already said, light years is the correct answer, give other peep brainiest
Answer and Explanation:
The Huntington disease is caused by a mutation in the gene that codifies for the Huntingtin protein (Htt). The mutation produces an altered form of the protein leading to the neuron´s death in certain areas of the brain.
The Huntington disease characterizes for being,
- Hereditary, passing from generation to generation. To express the disease, a person must have been born with an altered gene.
- Autosomal, affecting men and women equally, because the mutated gene is located on an autosomal chromosome.
- Dominant, which means that by getting only one copy of the altered gene coming from any of the parents, the receiving person will express the disease. The mutation in the gene dominates over the normal gene copy.
- Expressed by heterozygosis. Most people affected by the disease are heterozygous, with a normal copy and a mutated copy.
There are just a few cases all around the world (3% approximately) in which the disease is expressed with no family history. The progenitors are not affected by the mutation. These cases are very rare and are called <u>"de-novo" mutations.</u> A new mutation is spontaneously produced and it is not inherited from any of the parentals. It consists of an increase in the number of CAG repetitions. In a normal person, the number of CAG repetitions is less than 35. When there are 40 or more repetitions it occurs the disease. But when there are between 35 and 39 repetitions, the penetrance of the disease is incomplete. This is a "gray zone". Those alleles that fall in the gray zone are unstable and might produce the HD. Individuals with these unstable alleles have a tendency to increase the number of repetitions from generation to generation until the number reaches 40 repetitions and the person expresses the disease. This <u>usually occurs in the paternal germinal line</u>, as it is particularly unstable in sperm and probably meiosis greatly affects their instability, causing an increase in the number of CAG repeats.
