Definition:
Any material of plant, animal, microbial or other origin that carries genetic information and that passes it from one generation to the next.
The information contained controls reproduction, development, behaviour, etc.
Source: GreenFacts
More:
For all currently known living organisms the genetic material is almost exclusively DNA with the exception of some viruses and prions (infectious forms of normal proteins).
Source: GreenFacts
Related words:
Genes
Translation(s):
Español: Material genético
Français: Matériel génétique
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A genome is the complete set of genetic information in an organism. It provides all of the information the organism requires to function. In living organisms, the genome is stored in long molecules of DNA called chromosomes. Small sections of DNA, called genes, code for the RNA and protein molecules required by the organism. In eukaryotes, each cell's genome is contained within a membrane-bound structure called the nucleus. Prokaryotes, which contain no inner membranes, store their genome in a region of the cytoplasm called the nucleoid. The full range of RNA molecules expressed by a genome is known as its transcriptome, and the full assortment of proteins produced by the genome is called its proteome.
There are 23 pairs of chromosomes in the human genome. Between 1990 and 2003, all twenty-three pairs were fully sequenced through an international research undertaking known as the Human Genome Project. The study and analysis of genomes is called genomics.
The spiral structure in the picture is a large organic molecule. What type of organic molecule is it?
Here’s a hint: molecules like this one determine who you are. They contain genetic information that controls your characteristics. They determine your eye color, facial features, and other physical attributes. What molecule is it?
You probably answered "DNA." Today, it is commonly known that DNA is the genetic material. For a long time, scientists knew such molecules existed. They were aware that genetic information was contained within organic molecules. However, they didn’t know which type of molecules play this role. In fact, for many decades, scientists thought that proteins were the molecules that carry genetic information. In this section, you will learn how scientists discovered that DNA carries the code of life.
DNA, deoxyribonucleic acid, is the genetic material in your cells. It was passed on to you from your parents and determines your characteristics. The discovery that DNA is the genetic material was another important milestone in molecular biology.
Many scientists contributed to the identification of DNA as the genetic material. In the 1920s, Frederick Griffith made an important discovery. He was studying two different strains of a bacterium, called R (rough) strain and S (smooth) strain. He injected the two strains into mice. The S strain killed (virulent) the mice, but the R strain did not (non-virulent) (see Figure below). Griffith also injected mice with S-strain bacteria that had been killed by heat. As expected, the killed bacteria did not harm the mice. However, when the dead S-strain bacteria were mixed with live R-strain bacteria and injected, the mice died.
Griffith’s Experimental Results. Griffith showed that a substance could be transferred to harmless bacteria and make them deadly.
Based on his observations, Griffith deduced that something in the killed S strain was transferred to the previously harmless R strain, making the R strain deadly. He called this process transformation, as something was "transforming" the bacteria from one strain into another strain. What was that something? What type of substance could change the characteristics of the organism that received it?
In the early 1940s, a team of scientists led by Oswald Avery tried to answer the question raised by Griffith’s results. They inactivated various substances in the S-strain bacteria. They then killed the S-strain bacteria and mixed the remains with live R-strain bacteria. (Keep in mind, the R-strain bacteria usually did not harm the mice.) When they inactivated proteins, the R-strain was deadly to the injected mice. This ruled out proteins as the genetic material. Why? Even without the S-strain proteins, the R strain was changed, or transformed, into the deadly strain. However, when the researchers inactivated DNA in the S strain, the R strain remained harmless. This led to the conclusion that DNA is the substance that controls the characteristics of organisms. In other words, DNA is the genetic material. You can watch an animation about the research of both Griffith and Avery at this link://www.dnalc.org/view/16375-Animation-17-A-gene-is-made-of-DNA-.html.
The conclusion that DNA is the genetic material was not widely accepted at first. It had to be confirmed by other research. In the 1950s, Alfred Hershey and Martha Chase did experiments with viruses and bacteria. Viruses are not made of cells. They are basically DNA inside a protein coat. To reproduce, a virus must insert its own genetic material into a cell (such as a bacterium). Then it uses the cell’s machinery to make more viruses. The researchers used different radioactive elements to label the DNA and proteins in viruses. This allowed them to identify which molecule the viruses inserted into bacteria. DNA was the molecule they identified. This confirmed that DNA is the genetic material.
- The work of several researchers led to the discovery that DNA is the genetic material.
- Along the way, Griffith discovered the process of transformation.
- List the research that determined that DNA is the genetic material.
- What is transformation?
- What happened to the R-strain bacteria when Avery and his colleagues inactivated DNA in the S strain bacteria?
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During the early 19th century, it became widely accepted that all living organisms are composed of cells arising only from the growth and division of other cells. The improvement of the microscope then led to an era during which many biologists made intensive observations of the microscopic structure of cells. By 1885 a substantial amount of indirect evidence indicated that chromosomes—dark-staining threads in the cell nucleus—carried the information for cell heredity. It was later shown that chromosomes are about half DNA and half protein by weight. DNA structure The revolutionary discovery suggesting that DNA molecules could provide the information for their own replication came in 1953, when American geneticist and biophysicist James Watson and British biophysicist Francis Crick proposed a model for the structure of the double-stranded DNA molecule (called the DNA double helix). In this model, each strand serves as a template in the synthesis of a complementary strand. Subsequent research confirmed the Watson and Crick model of DNA replication and showed that DNA carries the genetic information for reproduction of the entire cell. All of the genetic information in a cell was initially thought to be confined to the DNA in the chromosomes of the cell nucleus. Later discoveries identified small amounts of additional genetic information present in the DNA of much smaller chromosomes located in two types of organelles in the cytoplasm. These organelles are the mitochondria in animal cells and the mitochondria and chloroplasts in plant cells. The special chromosomes carry the information coding for a few of the many proteins and RNA molecules needed by the organelles. They also hint at the evolutionary origin of these organelles, which are thought to have originated as free-living bacteria that were taken up by other organisms in the process of symbiosis. messenger RNA; translation It is possible for RNA to replicate itself by mechanisms related to those used by DNA, even though it has a single-stranded instead of a double-stranded structure. In early cells RNA is thought to have replicated itself in this way. However, all of the RNA in present-day cells is synthesized by special enzymes that construct a single-stranded RNA chain by using one strand of the DNA helix as a template. Although RNA molecules are synthesized in the cell nucleus, where the DNA is located, most of them are transported to the cytoplasm before they carry out their functions.
human disease: Abnormal growth of cells
) The growth of cells in the body is a closely controlled function, which, together with limited and regulated expression...
The RNA molecules in cells have two main roles. Some, the ribozymes, fold up in ways that allow them to serve as catalysts for specific chemical reactions. Others serve as “messenger RNA,” which provides templates specifying the synthesis of proteins. Ribosomes, tiny protein-synthesizing machines located in the cytoplasm, “read” the messenger RNA molecules and “translate” them into proteins by using the genetic code. In this translation, the sequence of nucleotides in the messenger RNA chain is decoded three nucleotides at a time, and each nucleotide triplet (called a codon) specifies a particular amino acid. Thus, a nucleotide sequence in the DNA specifies a protein provided that a messenger RNA molecule is produced from that DNA sequence. Each region of the DNA sequence specifying a protein in this way is called a gene.
By the above mechanisms, DNA molecules catalyze not only their own duplication but also dictate the structures of all protein molecules. A single human cell contains about 10,000 different proteins produced by the expression of 10,000 different genes. Actually, a set of human chromosomes is thought to contain DNA with enough information to express between 30,000 and 100,000 proteins, but most of these proteins seem to be made only in specialized types of cells and are therefore not present throughout the body. (For further discussion, see below The nucleus.)
A cell with its many different DNA, RNA, and protein molecules is quite different from a test tube containing the same components. When a cell is dissolved in a test tube, thousands of different types of molecules randomly mix together. In the living cell, however, these components are kept in specific places, reflecting the high degree of organization essential for the growth and division of the cell. Maintaining this internal organization requires a continuous input of energy, because spontaneous chemical reactions always create disorganization. Thus, much of the energy released by ATP hydrolysis fuels processes that organize macromolecules inside the cell.
When a eukaryotic cell is examined at high magnification in an electron microscope, it becomes apparent that specific membrane-bound organelles divide the interior into a variety of subcompartments. Although not detectable in the electron microscope, it is clear from biochemical assays that each organelle contains a different set of macromolecules. This biochemical segregation reflects the functional specialization of each compartment. Thus, the mitochondria, which produce most of the cell’s ATP, contain all of the enzymes needed to carry out the tricarboxylic acid cycle and oxidative phosphorylation. Similarly, the degradative enzymes needed for the intracellular digestion of unwanted macromolecules are confined to the lysosomes.
| cytosol | 54 | 1 |
| mitochondrion | 22 | 1,700 |
| endoplasmic reticulum plus Golgi apparatus | 15 | 1 |
| nucleus | 6 | 1 |
| lysosome | 1 | 300 |
It is clear from this functional segregation that the many different proteins specified by the genes in the cell nucleus must be transported to the compartment where they will be used. Not surprisingly, the cell contains an extensive membrane-bound system devoted to maintaining just this intracellular order. The system serves as a post office, guaranteeing the proper routing of newly synthesized macromolecules to their proper destinations.
All proteins are synthesized on ribosomes located in the cytosol. As soon as the first portion of the amino acid sequence of a protein emerges from the ribosome, it is inspected for the presence of a short “endoplasmic reticulum (ER) signal sequence.” Those ribosomes making proteins with such a sequence are transported to the surface of the ER membrane, where they complete their synthesis; the proteins made on these ribosomes are immediately transferred through the ER membrane to the inside of the ER compartment. Proteins lacking the ER signal sequence remain in the cytosol and are released from the ribosomes when their synthesis is completed. This chemical decision process places some newly completed protein chains in the cytosol and others within an extensive membrane-bounded compartment in the cytoplasm, representing the first step in intracellular protein sorting.
The newly made proteins in both cell compartments are then sorted further according to additional signal sequences that they contain. Some of the proteins in the cytosol remain there, while others go to the surface of mitochondria or (in plant cells) chloroplasts, where they are transferred through the membranes into the organelles. Subsignals on each of these proteins then designate exactly where in the organelle the protein belongs. The proteins initially sorted into the ER have an even wider range of destinations. Some of them remain in the ER, where they function as part of the organelle. Most enter transport vesicles and pass to the Golgi apparatus, separate membrane-bounded organelles that contain at least three subcompartments. Some of the proteins are retained in the subcompartments of the Golgi, where they are utilized for functions peculiar to that organelle. Most eventually enter vesicles that leave the Golgi for other cellular destinations such as the cell membrane, lysosomes, or special secretory vesicles. (For further discussion, see below Internal membranes.)