| LV | laryngeal vestibule; lateral ventricle; lecithovitellin; left ventricle, left ventricular; leucovori... |
|---|---|
| MDV | Marek disease virus; mean dye [bolus] velocity; mucosal disease virus |
| MLV | Moloney leukemia virus; multilaminar vesicle; murine leukemia virus |
| MSV | maximum sustained level of ventilation; mean scale value; mean spatial velocity; Moloney sarcoma vir... |
| MTV | mammary tumor virus; metatarsus varus; mouse mammary tumor virus |
| AP PCR | Arbitrary primed polymerase chain reaction |
|---|---|
| PARP | B/poly-ADP ribose polymerase |
| cPCR | Competitive polymerase chain reaction |
| DDRT-PCR | Differential Display Reverse Transcriptase Polymerase Chain Reaction |
| DD-PCR | Differential display polymerase chain reaction |
| DNA hybridization | A technique used to determine the relatedness of microorganisms by the speed and efficiency of the reassociation of single-stranded DNA to form double-stranded DNA when one of the strands originates from one organism and the other strand from another organism; occurs when the base sequences are complementary or nearly so. (05 Mar 2000) |
|---|---|
| DNA insertion elements | Discrete transposable segments of DNA which can insert into chromosomal, phage, and plasmid DNA. Some insert at random while others are site-specific; most have not been found to exist except in the inserted state. Their insertion into a genome always produces a mutation ("insertion mutation"), and their excision frequently results in a loss of host genetic information. Types of transposable elements include is elements (insertion sequence elements), which are composed of between 700 and 1400 bases and contain no genes unrelated to insertion function and tn elements (transposon elements), which are generally larger than 1400 bases and contain genes unrelated to insertion function. The concept also includes the delta element of saccharomyces cerevisiae and the integration site. (12 Dec 1998) |
| DNA iteron | <molecular biology> Repeated DNA sequence found near the origin of replication of some plasmids. (18 Nov 1997) |
| DNA, kinetoplast | Mitochondrial DNA of trypanosomes and related parasitic protozoa within the order kinetoplastida. Kinetoplast DNA is used as a DNA probe and consists of a complex network of numerous catenated rings of two classes; the first being a large number of small DNA duplex rings, called minicircles, approximately 2000 base pairs in length, and the second being several dozen much larger rings, called maxicircles, approximately 37 kb in length. (12 Dec 1998) |
| DNA library | <molecular biology> A collection of DNA molecules, derived from restriction fragments that have been cloned in vectors, that includes all or part of the genetic material of an organism. (18 Nov 1997) |
| DNA ligase | <enzyme, molecular biology> Enzyme involved in DNA replication. The DNA ligase of E. Coli seals nicks in one strand of double stranded DNA, a reaction required for linking precursor fragments during discontinuous synthesis on the lagging strand. Nicks are breaks in the phosphodiester linkage that leave a free 3_ OH and 5_ phosphate. The ligase from phage T4 has the additional property of joining two DNA molecules having completely base paired ends. DNA ligases are crucial in joining DNA molecules and preparing radioactive probes (by nick translation) in recombinant DNA technology. (18 Nov 1997) |
| DNA ligases | <enzyme> Poly(deoxyribonucleotide):poly(deoxyribonucleotide)ligases. Enzymes that catalyze the joining of preformed deoxyribonucleotides in phosphodiester linkage during genetic processes during repair of a single-stranded break in duplex DNA. The class includes both ATP and NAD. Registry number: EC 6.5.1.- (12 Dec 1998) |
| DNA ligation | <molecular biology> The joining of two DNA strands by their ends with a phosphodiester bond. (09 Oct 1997) |
| DNA markers | Segments of chromosomal DNA known to be linked with heritable traits or diseases. Although the markers themselves to not produce the conditions, they exist in concert with the genes responsible and are passed on with them. Certain markers, restriction fragment length polymorphisms, consist of segments of DNA that can be identified on autoradiographs (produced after digestion of the DNA by restriction enzymes and segregation of the resulting fragments through gel electrophoresis). (05 Mar 2000) |
| DNA melting | <molecular biology> Denaturation of a DNA molecule with heat. The double-stranded molecule breaks up into two single-stranded molecules as a result of heat. (09 Oct 1997) |
| DNA methylation | <molecular biology> Process by which methyl groups are added to certain nucleotides in genomic DNA. This affects gene expression, as methylated DNA is not easily transcribed. The degree of methylation is passed on to daughter strands at mitosis by maintainance DNA methylases. Accordingly, DNA methylation is thought to play an important developmental role in sequentially restricting the transcribable genes available to distinct cell lineages. In bacteria, methylation plays an important role in the restriction systems, as restriction enzymes cannot cut sequences with certain specific methylations. (18 Nov 1997) |
| DNA, mitochondrial | Double-stranded DNA of mitochondria. In eukaryotes, the mitochondrial genome is circular and codes for ribosomal rnas, transfer rnas, and about 10 proteins. (12 Dec 1998) |
| DNA modification | <molecular biology> A variety of chemical changes made to a DNA molecule just after it has been replicated. An example is DNA methylation. (09 Oct 1997) |
| DNA modification methylases | <enzyme> Enzymes that are part of the restriction-modification systems. They are responsible for producing a species-characteristic methylation pattern, on either adenine or cytosine residues, in a specific short base sequence in the host cell's own DNA. This methylated sequence will occur many times in the hosT-cell DNA and remain intact for the lifetime of the cell. Any DNA from another species which gains entry into a living cell and lacks the characteristic methylation pattern will be recognised by the restriction endonucleases of similar specificity and destroyed by cleavage. most have been studied in bacterial systems, but a few have been found in eukaryotic organisms. Registry number: EC 2.1.1.- (12 Dec 1998) |
| DNA molecules, recombinant | A combination of DNA molecules of different origin that are joined using recombinant DNA technology. (12 Dec 1998) |