The central dogma of life is an explanation of the flow of genetic information within a biological system. It is often stated as "DNA makes RNA and RNA makes protein. It was first stated by Francis Crick as “The Central Dogma - This states that once 'information' has passed into protein it cannot get out again. In more detail, the transfer of information from nucleic acid to nucleic acid, or from nucleic acid to protein may be possible, but transfer from protein to protein, or from protein to nucleic acid is impossible. Information means here the precise determination of sequence, either of bases in the nucleic acid or of amino acid residues in the protein”. [ Francis Crick, 1958].
The central dogma of life deals with the detailed residue-by-residue transfer of sequential information. It states that such information cannot be transferred back from protein to either protein or nucleic acid [Modified by Francis Crick, 1959].
DNA in cells exists as a double-stranded helix; the two strands are held together by hydrogen bonds between specific nitrogenous base pairs: A-T and C-G. A gene is a segment of DNA, a sequence of nucleotides, that code for a functional product, usually a protein. When a gene is expressed, DNA is transcribed to produce RNA; mRNA is then translated into proteins. The proteins cannot provide the genetic information from one generation to another. This is also referred as Central Dogma of Life. The DNA in a cell is replicated before the cell divides, so each daughter cell receives the same genetic information.
Because of this process, we could differentiate living and non-living things. Please note that some viruses do not possess the above by themselves - of course they use host systems - That's why we consider them as living system
Genetics is a discipline of biology, is the science of genes, heredity, and variation in living organisms. The word is derived from Ancient Greek word “genetikos”, (genitive) and that from genesis meaning origin.
Genetics deals with the
Gene is the genetic unit of function. A gene may encode a polypeptide or a molecule of non-translated RNA (e.g. ribosomal RNA, transfer RNA, or a regulatory RNA). As per the Mendel’s observation, gene is an unit of inheritance.
Given that genes are universal to living organisms, genetics can be applied to the study of all living systems, from viruses and bacteria, through plants and domestic animals, to humans.
DNA and Chromosomes
The DNA in a chromosome exists as one long double helix associated with various proteins that regulate genetic activity.
The eukaryotes have linear DNA fragmented into large-sized physical units called chromosomes. Whereas, the bacterial DNA is circular; the chromosome of E. coli, for example, contains about 4 million base pairs and is approximately 1000 times longer than the cell.
Genomics is the molecular characterization of genomes. Information contained in the DNA is transcribed into RNA and translated into proteins.
Enzymes that associated with DNA:
During DNA replication, the two strands of the double helix separate at the replication fork, and each strand is used as a template by DNA polymerases to synthesize two new strands of DNA according to the rules of nitrogenous base pairing.
The result of DNA replication is two new strands of DNA, each having a base sequence complementary to one of the original strands. Because each double-stranded DNA molecule contains one original and one new strand, the replication process is called as semiconservative. DNA is synthesized in one chemical direction called 5' to 3' (5' is phosphate end; 3' is hydroxyl end of deoxyribose). At the replication fork, the leading strand is synthesized continuously and the lagging strand, discontinuously. DNA polymerase proofreads new molecules of DNA and removes mismatched bases before continuing DNA synthesis. Errors only occur ~1 time for every 1010 bases added. Each daughter bacterium receives a chromosome identical to the parent's.
Transcription
During transcription, the enzyme RNA polymerase synthesizes a strand of RNA from one strand of double-stranded DNA, which serves as a template.
RNA is synthesized from nucleotides containing the bases A, C, G, and U, which pair with the bases of the DNA sense strand. The starting point for transcription, where RNA polymerase binds to DNA, is the promoter site; the region of DNA that is the endpoint of transcription is the terminator site; RNA is synthesized in the 5' to 3' direction.
Translation
Translation is the process in which the information in the nucleotide base sequence of mRNA is used to dictate the amino acid sequence of a protein.The mRNA associates with ribosomes, which consist of rRNA and protein. Three-base segments of mRNA that specify amino acids are called codons. The genetic code refers to the relationship among the nucleotide base sequence of DNA, the corresponding codons of mRNA, and the amino acids for which the codons code. The genetic code is degenerate; that is, most amino acids are coded for by more than one codon. Of the 64 codons, 61 are sense codons (which code for amino acids), and 3 are nonsense codons (stop codons) which do not code for amino acids and are stop signals for translation. The start codon, AUG, normally codes for methionine (formylmethionine at the beginning of a protein). Specific amino acids are attached to molecules of tRNA. Another portion of the tRNA has a base triplet called an anticodon. The base pairing of codon and anticodon at the ribosome results in specific amino acids being brought to the site of protein synthesis. The ribosome moves along the mRNA strand as amino acids are joined to form a growing polypeptide; mRNA is read in the 5' —> 3' direction. Translation ends when the ribosome reaches a stop codon on the mRNA.
BACTERIAL GENOME ORGANIZATION
DNA molecules that replicate as discrete genetic units in bacteria are called replicons. In some Escherichia coli strains, the chromosome is the only replicon present in the cell. Other bacterial strains have additional replicons, such as plasmids and bacteriophages.
Bacterial genomes vary in size from about 0.4 x 109 to 8.6 x 109 daltons (Da), some of the smallest being obligate parasites (Mycoplasma) and the largest belonging to bacteria capable of complex differentiation such as Myxococcus. The amount of DNA in the genome determines the maximum amount of information that it can encode. Most bacteria have a haploid genome, a single chromosome consisting of a circular, double stranded DNA molecule. However linear chromosomes have been found in Gram-positive Borrelia and Streptomyces spp., and one linear and one circular chromosome is present in the Gram-negative bacterium Agrobacterium tumefaciens.
The single chromosome of the common intestinal bacterium E. coli is 3 x 109 Da (4,500 kilobase pairs [kbp]) in size, accounting for about 2 to 3 percent of the dry weight of the cell. The E. coli genome is only about 0.1% as large as the human genome, but it is sufficient to code for several thousand polypeptides of average size (40 kDa or 360 amino acids).
The chromosome of E. coli has a contour length of approximately 1.35 mm, several hundred times longer than the bacterial cell, but the DNA is supercoiled and tightly packaged in the bacterial nucleoid. The time required for replication of the entire chromosome is about 40 minutes, which is approximately twice the shortest division time for this bacterium. DNA replication must be initiated as often as the cells divide, so in rapidly growing bacteria a new round of chromosomal replication begins before an earlier round is completed. At rapid growth rates there may be four chromosomes replicating to form eight at the time of cell division, which is coupled with completion of a round of chromosomal replication. Thus, the chromosome in rapidly growing bacteria is replicating at more than one point. The replication of chromosomal DNA in bacteria is complex and involves many different proteins.
Plasmids are replicons that are maintained as discrete, extra chromosomal genetic elements in bacteria. They are usually much smaller than the bacterial chromosome, varying from less than 5 to more than several hundred kbp, though plasmids as large as 2 Mbp occur in some bacteria. Plasmids usually encode traits that are not essential for bacterial viability, and replicate independently of the chromosome. Most plasmids are supercoiled, circular, double-stranded DNA molecules, but linear plasmids have also been demonstrated in Borrelia and Streptomyces.
Many plasmids control medically important properties of pathogenic bacteria, including resistance to one or several antibiotics, production of toxins, and synthesis of cell surface structures required for adherence or colonization. Plasmids that determine resistance to antibiotics are often called R plasmids (or R factors) and the plasmids responsible for conjugation are F plasmids.
Plasmids are classified based on their function in the host cell. Some of the important plasmids found in bacteria are:
Apart from these, some special plasmids are found in soil bacteria, which involve the plant-microbe interactions.