Page last updated: 2024-10-24

pyrimidine nucleoside transport

Definition

Target type: biologicalprocess

The directed movement of a pyrimidine nucleoside, a pyrimidine base covalently bonded to a ribose or deoxyribose sugar, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. [GOC:ai]

Pyrimidine nucleoside transport is a crucial biological process responsible for the uptake of pyrimidine nucleosides, such as cytidine, uridine, and thymidine, into cells. These nucleosides serve as precursors for the synthesis of DNA and RNA, making their transport essential for cell growth and proliferation.

The transport process is facilitated by specific membrane proteins known as nucleoside transporters. These transporters are integral membrane proteins that bind to pyrimidine nucleosides on one side of the membrane and facilitate their movement across the membrane to the other side. The transport mechanism is often coupled to the movement of ions, such as sodium or protons, creating a concentration gradient that drives nucleoside uptake.

Pyrimidine nucleoside transport is a highly regulated process influenced by factors such as substrate concentration, cell type, and physiological state. For instance, some cells express multiple nucleoside transporter isoforms, allowing for the selective uptake of specific nucleosides. Additionally, the expression and activity of these transporters can be modulated by signaling pathways and transcription factors, ensuring appropriate nucleoside levels within the cell.

There are two main types of pyrimidine nucleoside transporters: equilibrative nucleoside transporters (ENTs) and concentrative nucleoside transporters (CNTs). ENTs mediate passive diffusion of nucleosides across the membrane, driven by the concentration gradient. CNTs, on the other hand, utilize energy to transport nucleosides against their concentration gradient, resulting in accumulation of nucleosides inside the cell.

The importance of pyrimidine nucleoside transport is highlighted by its involvement in various physiological processes and diseases. Disruptions in nucleoside transport can lead to impaired DNA and RNA synthesis, leading to developmental abnormalities, immune deficiencies, and cancer. Conversely, nucleoside analogs, which are synthetic compounds that resemble natural pyrimidine nucleosides, are used as antiviral and anticancer drugs by targeting nucleoside transport and inhibiting viral or tumor cell proliferation.

In conclusion, pyrimidine nucleoside transport is a complex and essential biological process that ensures the availability of pyrimidine nucleosides for DNA and RNA synthesis, thereby supporting cell growth, proliferation, and various physiological functions. Disruptions in this process can have significant consequences for human health, highlighting its importance for maintaining cellular homeostasis.'
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Proteins (1)

ProteinDefinitionTaxonomy
Solute carrier family 28 member 3A solute carrier family 28 member 3 that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q9HAS3]Homo sapiens (human)

Compounds (10)

CompoundDefinitionClassesRoles
phloretindihydrochalconesantineoplastic agent;
plant metabolite
uridineuridinesdrug metabolite;
fundamental metabolite;
human metabolite
phlorhizinaryl beta-D-glucoside;
dihydrochalcones;
monosaccharide derivative
antioxidant;
plant metabolite
resacetophenone2',4'-dihydroxyacetophenone : A dihydroxyacetophenone that is acetophenone carrying hydroxy substituents at positions 2' and 4'.

resacetophenone: structure in first source
dihydroxyacetophenone;
resorcinols
plant metabolite
adenosinequinquefolan B: isolated from roots of Panax quinquefolium L.; RN not in Chemline 10/87; RN from Toxlitadenosines;
purines D-ribonucleoside
analgesic;
anti-arrhythmia drug;
fundamental metabolite;
human metabolite;
vasodilator agent
4-nitrobenzylthioinosine4-nitrobenzylthioinosine: inhibitor of nucleoside transport; acts on ENT1purine nucleoside
2,4,6-trihydroxyacetophenone2',4',6'-trihydroxyacetophenone : A benzenetriol that is acetophenone in which the hydrogens at positions 2, 4, and 6 on the phenyl group are replaced by hydroxy groups. It is used as a matrix in matrix-assisted laser desorption/ionization (MALDI) mass spectrometry for the analysis of acidic glycans and glycopeptides.

monoacetylphloroglucinol: structure in first source
aromatic ketone;
benzenetriol;
methyl ketone
MALDI matrix material;
plant metabolite
2,6-dihydroxyacetophenone2,6-dihydroxyacetophenone: inhibits aminopyrine-N-demethylase in rat liver microsomal preparationsaromatic ketone
tecadenosontecadenoson: an A1 adenosine receptor agonist
trilobatintrilobatin : An aryl beta-D-glucoside that is phloretin attached to a beta-D-glucopyranosyl residue at position 4' via a glycosidic linkage. It is isolated from the leaves of the Chinese sweet tea Lithocarpus polystachyus and exhibits significant anti-hyperglycemic, anti-oxidative and anti-inflammatory properties.

trilobatin: anti-inflammatory from Lithocarpus polystachyus leaves; structure in first source
aryl beta-D-glucoside;
dihydrochalcones;
monosaccharide derivative
anti-inflammatory agent;
antioxidant;
plant metabolite;
sweetening agent