Other stretches of DNA may be transcribed into small non-coding RNAs such as microRNA, transfer RNA (tRNA), small nucleolar RNA (snoRNA), small nuclear RNA (snRNA), or enzymatic RNA molecules called ribozymes[3] as well as larger non-coding RNAs such as ribosomal RNA (rRNA), and long non-coding RNA (lncRNA). After the first bond is synthesized, the RNA polymerase must escape the promoter. Some viruses (such as HIV, the cause of AIDS), have the ability to transcribe RNA into DNA. This produces an RNA molecule from 5' → 3', an exact copy of the coding strand (except that thymines are replaced with uracils, and the nucleotides are composed of a ribose (5-carbon) sugar where DNA has deoxyribose (one fewer oxygen atom) in its sugar-phosphate backbone). RNA sugar-phosphate backbone forms with assistance from RNA polymerase to form an RNA strand. An example of such an antibacterial is rifampicin, which inhibits bacterial transcription of DNA into mRNA by inhibiting DNA-dependent RNA polymerase by binding its beta-subunit, while 8-hydroxyquinoline is an antifungal transcription inhibitor. [5], Transcription has some proofreading mechanisms, but they are fewer and less effective than the controls for copying DNA. Such sites can be visualized by allowing engaged polymerases to extend their transcripts in tagged precursors (Br-UTP or Br-U) and immuno-labeling the tagged nascent RNA. Core promoters combined with general transcription factors are sufficient to direct transcription initiation, but generally have low basal activity. [32], Transcription inhibitors can be used as antibiotics against, for example, pathogenic bacteria (antibacterials) and fungi (antifungals). The segments of DNA transcribed into RNA molecules that can encode proteins are said to produce messenger RNA (mRNA). Phosphorylation of the transcription factor may activate it and that activated transcription factor may then activate the enhancer to which it is bound (see small red star representing phosphorylation of transcription factor bound to enhancer in the illustration). [14] Several cell function specific transcription factors (there are about 1,600 transcription factors in a human cell[15]) generally bind to specific motifs on an enhancer[16] and a small combination of these enhancer-bound transcription factors, when brought close to a promoter by a DNA loop, govern level of transcription of the target gene. [7] [35] When many of a gene's promoter CpG sites are methylated the gene becomes inhibited (silenced). [10] An enhancer localized in a DNA region distant from the promoter of a gene can have a very large effect on gene transcription, with some genes undergoing up to 100-fold increased transcription due to an activated enhancer. HIV has an RNA genome that is reverse transcribed into DNA. This directionality is because RNA polymerase can only add nucleotides to the 3' end of the growing mRNA chain. [18] An inactive enhancer may be bound by an inactive transcription factor. The enzyme ribonuclease H then digests the RNA strand, and reverse transcriptase synthesises a complementary strand of DNA to form a double helix DNA structure ("cDNA"). [20], Transcription begins with the binding of RNA polymerase, together with one or more general transcription factors, to a specific DNA sequence referred to as a "promoter" to form an RNA polymerase-promoter "closed complex". The term 'protist' is useful in describing those eukaryotes that are not within the Mediator (a complex usually consisting of about 26 proteins in an interacting structure) communicates regulatory signals from enhancer DNA-bound transcription factors directly to the RNA polymerase II (pol II) enzyme bound to the promoter. 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