Iron-sulfur cluster assembly enzyme
The ISCU gene provides instructions for making a protein called the iron-sulfur cluster assembly enzyme. As its name suggests, this enzyme is involved in the formation of clusters of iron and sulfur atoms (Fe-S clusters). Specifically, the enzyme acts as a platform, or scaffold, for the assembly of these clusters. Fe-S clusters are critical for the function of many different proteins, including those needed for DNA repair and the regulation of iron levels. Proteins containing Fe-S clusters are also necessary for energy production within mitochondria, which are the cell structures that convert the energy from food into a form that cells can use.
2. Health Conditions Related to Genetic Changes
2.1. Myopathy with Deficiency of Iron-Sulfur Cluster Assembly Enzyme
At least two mutations in the ISCU gene have been found to cause myopathy with deficiency of iron-sulfur cluster assembly enzyme. The more common mutation, written as IVS5+382G>C, alters the way the gene's instructions are pieced together to produce the enzyme. Most affected individuals have this mutation in both copies of the ISCU gene in each cell. The other mutation, which has been identified in one family, replaces the amino acid glycine with the amino acid glutamate at position 50 in the enzyme (written as Gly50Glu or G50E). Affected individuals in this family have had the G50E mutation in one copy of the ISCU gene in each cell and the IVS5+382G>C mutation in the other copy of the gene. This combination of mutations causes a severe variant of the disorder characterized by progressive muscle weakness and wasting.
Mutations in the ISCU gene severely limit the amount of iron-sulfur cluster assembly enzyme that is made in cells. A shortage of this enzyme prevents the normal production of proteins that contain Fe-S clusters, which disrupts a variety of cellular activities. A reduction in the amount of iron-sulfur cluster assembly enzyme is particularly damaging to skeletal muscle cells. Within the mitochondria of these cells, a lack of this enzyme causes problems with energy production and an overload of iron. These defects lead to muscle weakness, pain, and the other features of myopathy with deficiency of iron-sulfur cluster assembly enzyme.
3. Other Names for This Gene
iron-sulfur cluster scaffold homolog (E. coli)
IscU iron-sulfur cluster scaffold homolog
NifU-like N-terminal domain containing
nitrogen fixation cluster-like
The entry is from https://medlineplus.gov/genetics/gene/iscu
- Kollberg G, Tulinius M, Melberg A, Darin N, Andersen O, Holmgren D, Oldfors A,Holme E. Clinical manifestation and a new ISCU mutation in iron-sulphur clusterdeficiency myopathy. Brain. 2009 Aug;132(Pt 8):2170-9. doi: 10.1093/brain/awp152.
- Li K, Tong WH, Hughes RM, Rouault TA. Roles of the mammalian cytosoliccysteine desulfurase, ISCS, and scaffold protein, ISCU, in iron-sulfur clusterassembly. J Biol Chem. 2006 May 5;281(18):12344-51.
- Mochel F, Knight MA, Tong WH, Hernandez D, Ayyad K, Taivassalo T, Andersen PM,Singleton A, Rouault TA, Fischbeck KH, Haller RG. Splice mutation in theiron-sulfur cluster scaffold protein ISCU causes myopathy with exerciseintolerance. Am J Hum Genet. 2008 Mar;82(3):652-60. doi:10.1016/j.ajhg.2007.12.012.
- Olsson A, Lind L, Thornell LE, Holmberg M. Myopathy with lactic acidosis islinked to chromosome 12q23.3-24.11 and caused by an intron mutation in the ISCUgene resulting in a splicing defect. Hum Mol Genet. 2008 Jun 1;17(11):1666-72.doi: 10.1093/hmg/ddn057.
- Rouault TA, Tong WH. Iron-sulfur cluster biogenesis and human disease. Trends Genet. 2008 Aug;24(8):398-407. doi: 10.1016/j.tig.2008.05.008.Review.
- Tong WH, Rouault TA. Functions of mitochondrial ISCU and cytosolic ISCU inmammalian iron-sulfur cluster biogenesis and iron homeostasis. Cell Metab. 2006Mar;3(3):199-210.