Most genes contain the information needed to make functional molecules called proteins. (A few genes produce other molecules that help the cell assemble proteins.) The journey from gene to protein is complex and tightly controlled within each cell. It consists of two major steps: transcription and translation. Together, transcription and translation are known as gene expression.
During the process of transcription, the information stored in a gene's DNA is transferred to a similar molecule called RNA (ribonucleic acid) in the cell nucleus. Both RNA and DNA are made up of a chain of nucleotide bases, but they have slightly different chemical properties. The type of RNA that contains the information for making a protein is called messenger RNA (mRNA) because it carries the information, or message, from the DNA out of the nucleus into the cytoplasm.
Translation, the second step in getting from a gene to a protein, takes place in the cytoplasm. The mRNA interacts with a specialized complex called a ribosome, which "reads" the sequence of mRNA bases. Each sequence of three bases, called a codon, usually codes for one particular amino acid. (Amino acids are the building blocks of proteins.) A type of RNA called transfer RNA (tRNA) assembles the protein, one amino acid at a time. Protein assembly continues until the ribosome encounters a “stop” codon (a sequence of three bases that does not code for an amino acid).
The flow of information from DNA to RNA to proteins is one of the fundamental principles of molecular biology. It is so important that it is sometimes called the “central dogma.”
Through the processes of transcription and translation, information from genes is used to make proteins.
Answer:
A nurse observes a few small, yellow nodules on the cervix of a client during the speculum exam. They are not painful or odorous, and a thin, clear discharge is present. The nurse recognizes that these are most indicative of nabothian cysts.
Explanation:
Nabothian cysts or nabothian follicles are also called mucinous retention cysts or epithelial cysts. It is a mucus-filled cyst on the surface of the cervix. Many women have multiple cysts they are common, benign and considered a normal feature of the adult cervix. They may be translucent or opaque, whitish to yellow, and range from a few millimeters to 3 to 4 cm in diameter. They are most often caused when stratified squamous epithelium of the ectocervix which is the nearest portion to the vagina that grows over the simple columnar epithelium of the endocervix which is the nearest portion to the uterus.
There are no serious complications or threat to your health with nabothian cysts.
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Answer:
A genetic disorder that is inherited as a recessive trait is sickle cell anemia.
Explanation:
Sickle cell anemia can be described as a disorder which is caused by a mutation in the hemoglobin beta gene which is found on chromosome number 11. The pattern of inheritance of sickle cell anemia is autosomal recessive which means that both the alleles of the gene shall be recessive for the trait to occur. A person with one recessive allele for the trait will not carry the disease but will be a carrier for the disease.
