DNA is essentially a storage molecule. It contains all of the instructions a cell needs to sustain itself. These instructions are found within genes, which are sections of DNA made up of specific sequences of nucleotides. In order to be implemented, the instructions contained within genes must be expressed, or copied into a form that can be used by cells to produce the proteins needed to support life.
The instructions stored within DNA are read and processed by a cell in two steps: transcription and translation. Each of these steps is a separate biochemical process involving multiple molecules. During transcription, a portion of the cell's DNA serves as a template for creation of an RNA molecule. (RNA, or ribonucleic acid, is chemically similar to DNA, except for three main differences described later on in this concept page.) In some cases, the newly created RNA molecule is itself a finished product, and it serves an important function within the cell. In other cases, the RNA molecule carries messages from the DNA to other parts of the cell for processing. Most often, this information is used to manufacture proteins. The specific type of RNA that carries the information stored in DNA to other areas of the cell is called messenger RNA, or mRNA.
How does transcription proceed?
Transcription begins when an enzyme called RNA polymerase attaches to the DNA template strand and begins assembling a new chain of nucleotides to produce a complementary RNA strand. There are multiple types of types of RNA. In eukaryotes, there are multiple types of RNA polymerase which make the various types of RNA. In prokaryotes, a single RNA polymerase makes all types of RNA. Generally speaking, polymerases are large enzymes that work together with a number of other specialized cell proteins. These cell proteins, called transcription factors, help determine which DNA sequences should be transcribed and precisely when the transcription process should occur.
Starch is made up of alpha glucose. Fiber and Cellulose is made up of beta glucose.
Answer: he) is specified by the codons UUU and UUC, and the amino acid leucine (Leu) is specified by the codons CUU, CUC, CUA, and CUG.
Explanation:
Mutations present permanent and heritable changes in the genome. We distinguish gene and chromosome mutations. Mutations in the level of genes are called point mutations because only one to several nucleotides are changed. These processes are known as deletion, insertion, and substitution. Deletion presents a loss of nucleotides which changes DNA sequence. When new nucleotides are embedded in the DNA chain, it is known as insertion. Substitution implies the process where new nucleotides are inserted while the ones that were present in that specific spot in a DNA molecule are deleted.
Mutations can also appear in chromosomes altering their number and structure. There are four types of mutations - deletion, duplication, inversion, and translocation. In deletion, a whole or one part of a chromosome is lost. Duplication presents an extra copy of a whole or one part of a chromosome. In an inversion, parts of a chromosome change order, while in translocation a part of one chromosome detaches and then connects to another.
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