MIR17HG gene

miR-17-92a-1 cluster host gene

The MIR17HG gene provides instructions for making the miR-17~92 microRNA (miRNA) cluster. MiRNAs are short pieces of RNA, a chemical cousin of DNA. These molecules control gene expression by blocking protein production. The miR-17~92 cluster includes six miRNAs: miR-17, miR-18a, miR-19a, miR-19b-1, miR-20a, and miR-92a-1. MiRNAs in this cluster control the expression of hundreds of genes. These miRNAs help regulate signaling pathways that direct several cellular processes involved in growth and development, including cell growth and division (proliferation), cell maturation (differentiation), and the self-destruction of cells (apoptosis). Studies suggest that the miR-17~92 cluster is necessary for normal development of the skeleton, heart, kidneys, lungs, and nervous system.

The MIR17HG gene belongs to a class of genes known as oncogenes. When mutated, oncogenes have the potential to cause normal cells to become cancerous.

Genetic changes that reduce the amount of the MIR17HG gene cause Feingold syndrome type 2. This developmental disorder is characterized by abnormalities of the fingers and toes, particularly shortening of the second and fifth fingers (brachymesophalangy). Other common features include an unusually small head size (microcephaly) and learning disabilities. The mutations involved in this condition, known as 13q31.3 microdeletions, remove (delete) a small region of chromosome 13 that includes the MIR17HG gene and sometimes part or all of other nearby genes. Loss of the MIR17HG gene is thought to underlie the characteristic features of the disorder, although loss of other genes may play a role in some cases.

Deletion of one copy of the MIR17HG gene reduces the amount of miR-17~92 cluster miRNAs available to control the activity of specific genes during development before birth. While it is likely that the resulting disruption of signaling pathways leads to the problems with growth and development characteristic of Feingold syndrome type 2, it remains unclear exactly how a shortage of miR-17~92 cluster miRNAs causes the specific features of the condition.

Genetic changes that result in extra copies of the MIR17HG gene have been found in cancer. These genetic changes likely occur when DNA makes a copy of itself (replicates) in preparation for cell division. Errors in the replication process can result in one or more extra copies of a gene within a cell, which is known as gene amplification. The amplifications are somatic, which means they are not inherited but instead occur in cells that give rise to the tumor. Gene amplifications involving MIR17HG have been found in a cancer of immune system cells called diffuse large B-cell lymphoma. Such amplifications are thought to increase the amount of miR-17~92 miRNAs. The resulting alterations to cell signaling pathways may lead to too much cell proliferation or too little apoptosis. As a result, cells can grow and divide uncontrollably, leading to the development of cancer.

Genetic changes, called microduplications, that result in an extra copy of the MIR17HG gene have been associated with developmental problems in a small number of people. Some individuals with these microduplications have overgrowth of the skeleton, resulting in extra fingers (polydactyly) and an unusually large head size (macrocephaly). Others with these microduplications have impaired growth, leading to short fingers (brachydactyly) and short stature. Affected individuals may also have features of autism spectrum disorder, which is characterized by impaired communication and social interaction. Researchers suggest that an extra copy of the MIR17HG gene disrupts normal skeletal growth, although they are unsure why the microduplications can either increase or reduce growth.

Cytogenetic Location: 13q31.3, which is the long (q) arm of chromosome 13 at position 31.3

Molecular Location: base pairs 91,347,820 to 91,354,575 on chromosome 13 (Homo sapiens Annotation Release 109, GRCh38.p12) (NCBI)

Cytogenetic Location: 13q31.3, which is the long (q) arm of chromosome 13 at position 31.3
  • C13orf25
  • FGLDS2
  • FLJ14178
  • LINC00048
  • MIHG1
  • miR-17-92
  • MIRH1
  • MIRHG1
  • NCRNA00048