CRLF1 Gene

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1		Vicky Zhou	+ 478 word(s)	478	2020-12-15 07:49:05

This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/crlf1

cytokine receptor like factor 1

genes

1. Normal Function

The CRLF1 gene provides instructions for making a protein called cytokine receptor-like factor 1 (CRLF1). This protein partners with a similar protein called cardiotrophin-like cytokine factor 1 (CLCF1), which is produced from the CLCF1 gene. Together, these two proteins form a unit known as the CRLF1/CLCF1 protein complex. This complex attaches (binds) to a receptor protein known as the ciliary neurotrophic factor receptor (CNTFR) on the surface of many types of cells. When the CRLF1/CLCF1 protein complex is bound to CNTFR, it triggers signaling inside the cell that affects cell development and function.

The CNTFR signaling pathway is primarily involved in the development and maintenance of the nervous system. It promotes the survival of nerve cells (neurons), particularly nerve cells that control muscle movement (motor neurons). The CNTFR pathway also plays a role in a part of the nervous system called the sympathetic nervous system, specifically in the regulation of sweating in response to temperature changes and other factors. This signaling pathway appears to be critical for the normal development and maturation of nerve cells that control the activity of sweat glands.

Studies suggest that the CNTFR signaling pathway also has functions outside the nervous system. It may be involved in the body's inflammatory response, which helps fight infection and facilitate tissue repair following an injury. This pathway may also be important for the development and maintenance of bone tissue. However, little is known about the role of CNTFR signaling in these processes.

2. Health Conditions Related to Genetic Changes

Cold-induced sweating syndrome

At least 10 mutations in the CRLF1 gene have been reported to cause cold-induced sweating syndrome, a rare condition characterized by problems with regulating body temperature and other abnormalities affecting many parts of the body. When this condition is caused by CRLF1 gene mutations, it is known as CISS1.

Mutations in the CRLF1 gene lead to the production of a nonfunctional version of the CRLF1 protein or greatly reduce the production of functional CRLF1 protein. Consequently, CRLF1 is unavailable to interact with the CLCF1 protein and bind to CNTFR, which disables the CNTFR signaling pathway.

Researchers believe that a failure of CNTFR signaling underlies the major features of cold-induced sweating syndrome. A loss of this signaling pathway during sympathetic nervous system development may help explain the abnormal sweating that is characteristic of this condition, including unusual sweating patterns and related problems with body temperature regulation. The CNTFR pathway's involvement in motor neuron development and bone development provides clues to some of the other signs and symptoms of the disorder, including distinctive facial features, facial muscle weakness, and skeletal abnormalities. However, little is known about how a lack of CNTFR signaling leads to these varied features.

3. Other Names for This Gene

CISS
CISS1
class I cytokine receptor
CLF
CLF-1
CRLF1_HUMAN
cytokine receptor-like factor 1
cytokine type 1 receptor CRLP-1
cytokine-like factor 1
zcytor5

References

Crisponi L, Crisponi G, Meloni A, Toliat MR, Nurnberg G, Usala G, Uda M,Masala M, Hohne W, Becker C, Marongiu M, Chiappe F, Kleta R, Rauch A, Wollnik B, Strasser F, Reese T, Jakobs C, Kurlemann G, Cao A, Nurnberg P, Rutsch F. Crisponisyndrome is caused by mutations in the CRLF1 gene and is allelic to cold-induced sweating syndrome type 1. Am J Hum Genet. 2007 May;80(5):971-81.
Dagoneau N, Bellais S, Blanchet P, Sarda P, Al-Gazali LI, Di Rocco M, Huber C,Djouadi F, Le Goff C, Munnich A, Cormier-Daire V. Mutations in cytokinereceptor-like factor 1 (CRLF1) account for both Crisponi and cold-inducedsweating syndromes. Am J Hum Genet. 2007 May;80(5):966-70.
Elson GC, Graber P, Losberger C, Herren S, Gretener D, Menoud LN, Wells TN,Kosco-Vilbois MH, Gauchat JF. Cytokine-like factor-1, a novel soluble protein,shares homology with members of the cytokine type I receptor family. J Immunol.1998 Aug 1;161(3):1371-9.
Hahn AF, Jones DL, Knappskog PM, Boman H, McLeod JG. Cold-induced sweatingsyndrome: a report of two cases and demonstration of genetic heterogeneity. JNeurol Sci. 2006 Dec 1;250(1-2):62-70.
Hahn AF, Waaler PE, Kvistad PH, Bamforth JS, Miles JH, McLeod JG, KnappskogPM, Boman H. Cold-induced sweating syndrome: CISS1 and CISS2: manifestations frominfancy to adulthood. Four new cases. J Neurol Sci. 2010 Jun 15;293(1-2):68-75.doi: 10.1016/j.jns.2010.02.028.
Herholz J, Meloni A, Marongiu M, Chiappe F, Deiana M, Herrero CR, Zampino G,Hamamy H, Zalloum Y, Waaler PE, Crisponi G, Crisponi L, Rutsch F. Differentialsecretion of the mutated protein is a major component affecting phenotypicseverity in CRLF1-associated disorders. Eur J Hum Genet. 2011 May;19(5):525-33.doi: 10.1038/ejhg.2010.253.
Kass DJ. Cytokine-like factor 1 (CLF1): life after development? Cytokine. 2011Sep;55(3):325-9. doi: 10.1016/j.cyto.2011.05.021.
Knappskog PM, Majewski J, Livneh A, Nilsen PT, Bringsli JS, Ott J, Boman H.Cold-induced sweating syndrome is caused by mutations in the CRLF1 gene. Am J HumGenet. 2003 Feb;72(2):375-83.

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Subjects: Genetics & Heredity

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Vicky Zhou

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Entry Collection: MedlinePlus

Update Date: 24 Dec 2020

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