The nucleic acid are Macromolécule S, i.e. large relatively complex molecules. They enter the family of the Biomolécule S since they are of very great importance in the reign of the life, “ bio ” meaning life in Greek.
The nucleic acid are Polymère S of which the basic unit, or Monomère, is the Nucléotide. These nucleotides are related the ones to the others by connections phosphodiester.
The DNA is in the cellular core at the Eucaryote S. It joins Protéine S like Histone S. This fitting of DNA and proteins forms the Chromatine which one finds in the form of linear Chromosome S at the Eucaryote S (quite visible during the Mitose) and in the form of single helicoid chromosome at the Procaryote S. For its part, the ARN is found as much on the level of the core as on the level of the Cytosol.
The connections phosphodiester are covalent bonds . (One can say that all the connections phophodiester are covalent bonds, but all the covalent bonds are not connections phophodiester).
Put aside, hydrogen bonds, that one often names hydrogen interactions because makes of it, it does not have “connection” itself there, any other connection present in the nucleic acids are covalent connections .
The skeleton is a relatively rigid part since it is composed of covalent bonds, of the very strong chemical bonds.
This flexible structure is ideal to allow the Protéine S the such Polymérase S, the Primase S and the Ligase S, to translate or duplicate the DNA.
the ARN messenger (ARNm) : is the product of the épissage of the ARN prémessager (ARNpm), which is to him the product of the transcription operated on the DNA. the ARN prémessager is also called heterogeneous ARN nuclear (ARNnh) because it is found strictly in the core and is composed of Intron S and of Exon S. the épissage of ARNpm consists in removing will introns them and to connect let us exons them the ones following the others. This chain of let us exons then constitutes the ARN messenger “finished product”. Contrary to the ARN prémessager, the ARN messenger leaves the core and ultimement is ultimement translated into Peptide in the cytosol or in the endoplasmic Réticulum. ARNm is the “plan of construction” of a Protéine. There is no épissage at the Procaryote S where the ARN produced by the transcription is directly ARNm (indeed these organizations do not have a core and ribosomes are fixed on the molecule of ARN while it is synthesized).
the ARN of transfer (ARNt) : is implied at the time of the translation of the ARN messenger in Peptide. It is charged to bring the amino-acid goods by deciphering the language which constitute code them and to translate them into sequence Amino-acid . A codon consists of three Nucléotide S adjacent. A codon corresponds to only one Amino-acid, but the same amino-acid can be specified by different code.
See genetic Code to know which amino-acids are associated with which code.
|The ribosomal ARN (ARNr) : constitute the Ribosome after maturation and association with Protéine S. the Ribosome S are manufacturing planies of Protéine S. ribosome joins the ARN messenger and “reads” the Codon S which are found there. It manages then the entry and the exit of the ARN of transfer which transport the amino-acid . The birth of a Peptide follows which will be possibly, after several stages of maturation and assembly, transformed into Protéine.
the microARN (miARN) : discovered in 1993 by Victor Ambros in the worm Caenorhabditis elegans. They have a structure simple bit and are long of 19 to 25 nucleotides. They play a part in the cellular metabolism by preventing the translation some ARN messenger in Peptide S. While binding to ARN messengers of which they are partially complementary, the microARN involve the blocking of the translation of ARNm by ribosomes.
the silencingRNA (siRNA) are small ARN of 21-22 nucleotides perfectly complementary to their ARNm targets. Contrary to the miRNA, the siRNA are not coded by the genome of the host cell but rather not brought by a possible invader such as the viruses. Moreover, they have a structure in double bit, and their action consists in degrading ARNm. It is carried out in collaboration with proteins called RISC (RNA Induced Silencing Complex). These last set on the bit antisens (complementary to the coding bit) siARN, the bit direction is abandoned, and the complex (RISC + ARN simple bit antisens) thus formed can recognize the fragment of corresponding ARNm and destroy it, thus preventing the form of associated gene.
These short ARN became a tool very much used in molecular biology to one by one extinguish the genes whose one wishes to determine the metabolic role. Their specificity of action makes siARN a way very studied in the fight against cancer and the viral diseases.
snRNA (small nuclear RNA), snoRNA (small nucleolus RNA), scaRNA (small cajal bodies RNA): they are short chains of ribonucléotides (which is found exclusively in the core and more precisely in compartments of the core like the nucleole Pr the snoRNA and the bodies of Cajal for the scaRNA. These ARN not coding join proteins to form named complexes small ribonucleoproteins nuclear (RNPpn), essential during the process of épissage of ARN prémessagers and during the process of maturation of ARNr and ARNtm
Let us note that one separates the viruses in several classes, according to the form under which is presented the Genetic material virus. Thus the HIV, the virus transmitting the AIDS, are a Rétrovirus, or virus with ARN because its genetic material is presented in the form of ARN inside its Capside. In a general way, there is no particular name for the viruses with DNA.
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