Skip Navigation
Genetics Home Reference: your guide to understanding genetic conditions
http://ghr.nlm.nih.gov/     A service of the U.S. National Library of Medicine®

TGFBR2

Reviewed July 2014

What is the official name of the TGFBR2 gene?

The official name of this gene is “transforming growth factor, beta receptor II (70/80kDa).”

TGFBR2 is the gene's official symbol. The TGFBR2 gene is also known by other names, listed below.

What is the normal function of the TGFBR2 gene?

The TGFBR2 gene provides instructions for making a protein called transforming growth factor-beta (TGF-β) receptor type 2. This receptor transmits signals from the cell surface into the cell through a process called signal transduction. Through this type of signaling, the environment outside the cell affects activities inside the cell such as stimulation of cell growth and division.

To carry out its signaling function, the TGF-β receptor type 2 spans the cell membrane, so that one end of the protein projects from the outer surface of the cell (the extracellular domain) and the other end remains inside the cell (the intracellular domain). A protein called TGF-β attaches (binds) to the extracellular domain of the TGF-β receptor type 2, which turns on (activates) the receptor and allows it to bind to a similar receptor on the cell surface. These three proteins form a complex, which triggers signal transduction by activating other proteins in this signaling pathway.

Signals triggered through the TGF-β receptor complex prompt various responses by the cell, including the growth and division (proliferation) of cells, the maturation of cells to carry out specific functions (differentiation), cell movement (motility), and controlled cell death (apoptosis). Because TGF-β receptor type 2 keeps cells from growing and dividing too rapidly or in an uncontrolled way, it is also important in suppressing the formation of tumors.

How are changes in the TGFBR2 gene related to health conditions?

Loeys-Dietz syndrome - caused by mutations in the TGFBR2 gene

More than 80 mutations in the TGFBR2 gene have been found to cause Loeys-Dietz syndrome type II. Loeys-Dietz syndrome affects connective tissue, which gives structure and support to blood vessels, the skeleton, and other parts of the body. This type of Loeys-Dietz syndrome is characterized by blood vessel abnormalities and skeletal deformities. Most TGFBR2 gene mutations that cause Loeys-Dietz syndrome change single protein building blocks (amino acids) in TGF-β receptor type 2, resulting in a receptor with little or no function. Although the receptor has severely reduced function, cell signaling occurs at an even greater intensity than normal. Researchers speculate that the activity of proteins in this signaling pathway is increased to compensate for the reduction in TGF-β receptor type 2 activity; however the exact mechanism responsible for the increase in signaling is unclear. The overactive signaling pathway disrupts development of connective tissue and various body systems and leads to the varied signs and symptoms of Loeys-Dietz syndrome type II.

Some TGFBR2 gene mutations that cause Loeys-Dietz syndrome type II have also been found to cause familial thoracic aortic aneurysm and dissection (TAAD) (described below). Affected families can include some individuals with Loeys-Dietz syndrome and others with familial TAAD.

cancers - increased risk from variations of the TGFBR2 gene

Some TGFBR2 gene mutations are acquired during a person's lifetime and are present only in certain cells. These changes are called somatic mutations and are not inherited. People with somatic mutations in the TGFBR2 gene appear to have an increased risk of developing various cancers. Somatic TGFBR2 gene mutations probably disrupt the signaling process that helps regulate cell division. Unchecked cell division can lead to the formation of tumors, particularly when TGFBR2 gene mutations occur in the colon, rectum, and esophagus. It is estimated that 30 percent of cancerous (malignant) colon tumors have TGFBR2 gene mutations in their cells.

familial thoracic aortic aneurysm and dissection - increased risk from variations of the TGFBR2 gene

At least nine TGFBR2 gene mutations have been identified in people with familial thoracic aortic aneurysm and dissection (familial TAAD). This disorder involves problems with the aorta, which is the large blood vessel that distributes blood from the heart to the rest of the body. The aorta can weaken and stretch, causing a bulge in the blood vessel wall (an aneurysm). Stretching of the aorta may also lead to a sudden tearing of the layers in the aorta wall (aortic dissection). Aortic aneurysm and dissection can be life threatening.

The TGFBR2 gene mutations that cause familial TAAD disturb signal transduction. The disturbed signaling can impair cell growth and development. It is not known how these changes result in the specific aortic abnormalities associated with familial TAAD.

Where is the TGFBR2 gene located?

Cytogenetic Location: 3p22

Molecular Location on chromosome 3: base pairs 30,606,501 to 30,694,141

The TGFBR2 gene is located on the short (p) arm of chromosome 3 at position 22.

The TGFBR2 gene is located on the short (p) arm of chromosome 3 at position 22.

More precisely, the TGFBR2 gene is located from base pair 30,606,501 to base pair 30,694,141 on chromosome 3.

See How do geneticists indicate the location of a gene? (http://ghr.nlm.nih.gov/handbook/howgeneswork/genelocation) in the Handbook.

Where can I find additional information about TGFBR2?

You and your healthcare professional may find the following resources about TGFBR2 helpful.

You may also be interested in these resources, which are designed for genetics professionals and researchers.

What other names do people use for the TGFBR2 gene or gene products?

  • AAT3
  • FAA3
  • HNPCC6
  • MFS2
  • RIIC
  • TAAD2
  • TGF-beta receptor type IIB
  • TGFbeta-RII
  • TGF-beta type II receptor
  • TGFR-2
  • TGFR2_HUMAN

See How are genetic conditions and genes named? (http://ghr.nlm.nih.gov/handbook/mutationsanddisorders/naming) in the Handbook.

What glossary definitions help with understanding TGFBR2?

acids ; aneurysm ; aorta ; aortic dissection ; apoptosis ; cell ; cell division ; cell membrane ; colon ; connective tissue ; differentiation ; domain ; esophagus ; extracellular ; familial ; gene ; growth factor ; inherited ; intracellular ; proliferation ; protein ; receptor ; rectum ; signal transduction ; syndrome ; tissue ; transduction

You may find definitions for these and many other terms in the Genetics Home Reference Glossary (http://www.ghr.nlm.nih.gov/glossary).

References

  • Biswas S, Trobridge P, Romero-Gallo J, Billheimer D, Myeroff LL, Willson JK, Markowitz SD, Grady WM. Mutational inactivation of TGFBR2 in microsatellite unstable colon cancer arises from the cooperation of genomic instability and the clonal outgrowth of transforming growth factor beta resistant cells. Genes Chromosomes Cancer. 2008 Feb;47(2):95-106. (http://www.ncbi.nlm.nih.gov/pubmed/17985359?dopt=Abstract)
  • Frederic MY, Hamroun D, Faivre L, Boileau C, Jondeau G, Claustres M, Béroud C, Collod-Béroud G. A new locus-specific database (LSDB) for mutations in the TGFBR2 gene: UMD-TGFBR2. Hum Mutat. 2008 Jan;29(1):33-8. (http://www.ncbi.nlm.nih.gov/pubmed/17935258?dopt=Abstract)
  • Loeys BL, Chen J, Neptune ER, Judge DP, Podowski M, Holm T, Meyers J, Leitch CC, Katsanis N, Sharifi N, Xu FL, Myers LA, Spevak PJ, Cameron DE, De Backer J, Hellemans J, Chen Y, Davis EC, Webb CL, Kress W, Coucke P, Rifkin DB, De Paepe AM, Dietz HC. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2. Nat Genet. 2005 Mar;37(3):275-81. Epub 2005 Jan 30. (http://www.ncbi.nlm.nih.gov/pubmed/15731757?dopt=Abstract)
  • Loeys BL, Schwarze U, Holm T, Callewaert BL, Thomas GH, Pannu H, De Backer JF, Oswald GL, Symoens S, Manouvrier S, Roberts AE, Faravelli F, Greco MA, Pyeritz RE, Milewicz DM, Coucke PJ, Cameron DE, Braverman AC, Byers PH, De Paepe AM, Dietz HC. Aneurysm syndromes caused by mutations in the TGF-beta receptor. N Engl J Med. 2006 Aug 24;355(8):788-98. (http://www.ncbi.nlm.nih.gov/pubmed/16928994?dopt=Abstract)
  • NCBI Gene (http://www.ncbi.nlm.nih.gov/gene/7048)
  • Pannu H, Fadulu VT, Chang J, Lafont A, Hasham SN, Sparks E, Giampietro PF, Zaleski C, Estrera AL, Safi HJ, Shete S, Willing MC, Raman CS, Milewicz DM. Mutations in transforming growth factor-beta receptor type II cause familial thoracic aortic aneurysms and dissections. Circulation. 2005 Jul 26;112(4):513-20. Epub 2005 Jul 18. (http://www.ncbi.nlm.nih.gov/pubmed/16027248?dopt=Abstract)
  • Pezzini A, Del Zotto E, Giossi A, Volonghi I, Costa P, Padovani A. Transforming growth factor β signaling perturbation in the Loeys-Dietz syndrome. Curr Med Chem. 2012;19(3):454-60. Review. (http://www.ncbi.nlm.nih.gov/pubmed/22335518?dopt=Abstract)
  • OMIM: TRANSFORMING GROWTH FACTOR-BETA RECEPTOR, TYPE II (http://omim.org/entry/190182)
  • Van Hemelrijk C, Renard M, Loeys B. The Loeys-Dietz syndrome: an update for the clinician. Curr Opin Cardiol. 2010 Nov;25(6):546-51. doi: 10.1097/HCO.0b013e32833f0220. Review. (http://www.ncbi.nlm.nih.gov/pubmed/20838339?dopt=Abstract)

 

The resources on this site should not be used as a substitute for professional medical care or advice. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional. See How can I find a genetics professional in my area? (http://ghr.nlm.nih.gov/handbook/consult/findingprofessional) in the Handbook.

 
Reviewed: July 2014
Published: November 24, 2014