4.8 Article

MED12, the Mediator Complex Subunit 12 Gene, Is Mutated at High Frequency in Uterine Leiomyomas

Journal

SCIENCE
Volume 334, Issue 6053, Pages 252-255

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1208930

Keywords

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Funding

  1. Academy of Finland (Center of Excellence in Translational Genome-Scale Biology) [6302352, 1124270, 212901, 214323]
  2. European Commission [2005-518200]
  3. GENICA Genomic Instability in Cancer and Precancer [201630]
  4. Sigrid Juselius Foundation
  5. Cancer Society of Finland
  6. Academy of Finland (AKA) [214323, 212901, 212901, 214323] Funding Source: Academy of Finland (AKA)

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Uterine leiomyomas, or fibroids, are benign tumors that affect millions of women worldwide and that can cause considerable morbidity. To study the genetic basis of this tumor type, we examined 18 uterine leiomyomas derived from 17 different patients by exome sequencing and identified tumor-specific mutations in the mediator complex subunit 12 (MED12) gene in 10. Through analysis of 207 additional tumors, we determined that MED12 is altered in 70% (159 of 225) of tumors from a total of 80 patients. The Mediator complex is a 26-subunit transcriptional regulator that bridges DNA regulatory sequences to the RNA polymerase II initiation complex. All mutations resided in exon 2, suggesting that aberrant function of this region of MED12 contributes to tumorigenesis.

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