Biology:ANO5

Short description: Protein-coding gene in the species Homo sapiens

Generic protein structure example

Anoctamin 5 (ANO5) is a protein that in humans is encoded by the ANO5 gene.

Function

The ANO5 gene provides instructions for making a protein called anoctamin-5. While the specific function of this protein is not well understood, it belongs to a family of proteins, called anoctamins, that act as chloride channels. Chloride channels, which transport negatively charged chlorine atoms (chloride ions) in and out of cells, play a key role in a cell's ability to generate and transmit electrical signals. Most anoctamin proteins function as chloride channels that are turned on (activated) in the presence of positively charged calcium atoms (calcium ions); these channels are known as calcium-activated chloride channels. The mechanism for this calcium activation is unclear. Anoctamin proteins are also involved in maintaining the membrane that surrounds cells and repairing the membrane if damaged.

The anoctamin-5 protein is most abundant in muscles used for movement (skeletal muscles). For the body to move normally, skeletal muscles must tense (contract) and relax in a coordinated way. The regulation of chloride flow within muscle cells plays a role in controlling muscle contraction and relaxation.

The anoctamin-5 protein is also found in other cells including heart (cardiac) muscle cells and bone cells. The anoctamin-5 protein may be important for the development of muscle and bone before birth.

Clinical significance

Mutations in the ANO5 gene are known to cause the following conditions:

• Gnathodiaphyseal dysplasia (GDD), a rare skeletal syndrome.
• Limb Girdle Muscular Dystrophy 2L (LGMD2L, Autosomal Recessive 12) and Miyoshi Muscular Dystrophy 3 (MMD3). These forms of muscular dystrophy are inherited in an autosomal recessive pattern. To be affected, a person must have mutations on both copies of the gene. Males and females are equally likely to be affected.

Typical Symptoms

GDD causes bone fragility, sclerosis of tubular bones, and cemento-osseous lesions of the jawbone. Patients also experience frequent bone fractures.

Clinically, LGMD2L and MMD3 were considered different diseases before ANO5 was identified as the responsible gene; LGMD was used to describe initial weakness in proximal muscles (hip and shoulder girdles) while MMD described initial weakness in the distal muscles of the lower limbs.

Other names for this gene

• ANO5_HUMAN
• anoctamin-5
• GDD1
• gnathodiaphyseal dysplasia 1 protein
• integral membrane protein GDD1
• LGMD2L
• TMEM16E
• transmembrane protein 16E

Chromosal location

• Cytogenetic location: 11p14.3, which is the short (p) arm of chromosome 11 at position 14.3
• Molecular location: base pairs 22,192,485 to 22,283,367 on chromosome 11 (Homo sapiens Annotation Release 109, GRCh38.p12) (NCBI)

Credit: Genome Decoration Page/NCBI

Further reading

• "ANO5-Related Muscle Diseases". SourceGeneReviews [Internet]. Seattle (WA): University of Washington, Seattle. November 2012. https://www.ncbi.nlm.nih.gov/books/NBK114459/. 
• "What is LGMD2L?". LGMD2L foundation. https://www.lgmd2l-foundation.org/. 
• Online Mendelian Inheritance in Man (OMIM) ANOCTAMIN 5; ANO5 -608662
• "Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies". American Journal of Human Genetics 86 (2): 213–21. February 2010. doi:10.1016/j.ajhg.2009.12.013. PMID 20096397. 
• "ANO5 mutations in the Polish limb girdle muscular dystrophy patients: Effects on the protein structure". Scientific Reports 9 (1): 11533. August 2019. doi:10.1038/s41598-019-47849-3. PMID 31395899. Bibcode: 2019NatSR...911533J. 

External links

• LGMD2L Foundation
• Myonexus Therapeudics
• Online Mendelian Inheritance in Man (OMIM) MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L; LGMD2L -611307
• Novel ANO5 KO mouse provides new insight into LGMD2L pathogenesis
• wolframalpha ano5