SLC29A3 gene

solute carrier family 29 member 3

The SLC29A3 gene provides instructions for making a protein called equilibrative nucleoside transporter 3 (ENT3). ENT3 belongs to a family of proteins that transport molecules called nucleosides in cells. With chemical modification, nucleosides become the building blocks of DNA, its chemical cousin RNA, and molecules such as ATP and GTP, which serve as energy sources in the cell. Molecules derived from nucleosides play an important role in many functions throughout the body.

ENT3 is found in the membranes surrounding cell structures known as lysosomes and mitochondria. Lysosomes are compartments within the cell that use digestive enzymes to break down large molecules into smaller ones that can be reused by cells. Researchers believe that ENT3 transports nucleosides generated by the breakdown of DNA and RNA out of lysosomes into the cell so they can be reused.

Mitochondria are structures within cells that convert the energy from food into a form that cells can use. While most DNA is packaged in chromosomes within the nucleus, mitochondria also have a small amount of their own DNA (called mitochondrial DNA). Researchers believe that the ENT3 protein in mitochondrial membranes helps transport nucleosides into mitochondria; the nucleosides can then be used for the formation or repair of mitochondrial DNA and RNA, which are essential for proper functioning of the structures.

Mutations in the SLC29A3 gene cause histiocytosis-lymphadenopathy plus syndrome, which is a group of conditions with overlapping signs and symptoms that affect many parts of the body. A feature common to the disorders in this spectrum is histiocytosis, which is the overgrowth of immune system cells called histiocytes. These cells abnormally accumulate in tissues, often in the lymph nodes of the neck. Buildup of these cells in the lymph nodes causes swelling of the lymph nodes (lymphadenopathy). Other features can include unusually dark (hyperpigmented) skin patches with excessive hair growth (hypertrichosis), diabetes, and hearing loss.

The SLC29A3 gene mutations involved in this spectrum of disorders reduce or eliminate the activity of the ENT3 protein. Researchers are unsure how loss of ENT3 activity causes histiocytosis and other features of histiocytosis-lymphadenopathy plus syndrome. They speculate that the resulting impairment of nucleoside transport leads to a buildup of nucleosides in lysosomes and possibly in other cellular structures. The excess nucleosides may be damaging to cell function. A lack of ENT3 activity can also lead to a reduction in the amount of nucleosides in mitochondria. This nucleoside shortage could impair cellular energy production, which would impact many body systems. It is unclear how SLC29A3 gene mutations cause different patterns of signs and symptoms, even within the same family.

Cytogenetic Location: 10q22.1, which is the long (q) arm of chromosome 10 at position 22.1

Molecular Location: base pairs 71,319,253 to 71,363,390 on chromosome 10 (Homo sapiens Annotation Release 108, GRCh38.p7) (NCBI)

Cytogenetic Location: 10q22.1, which is the long (q) arm of chromosome 10 at position 22.1
  • ENT3
  • equilibrative nucleoside transporter 3
  • FLJ11160
  • HJCD
  • PHID
  • solute carrier family 29 (equilibrative nucleoside transporter), member 3
  • solute carrier family 29 (nucleoside transporters), member 3