Abstract:
:Insulinomas are pancreatic islet tumors that inappropriately secrete insulin, producing hypoglycemia. Exome and targeted sequencing revealed that 14 of 43 insulinomas harbored the identical somatic mutation in the DNA-binding zinc finger of the transcription factor Yin Yang 1 (YY1). Chromatin immunoprecipitation sequencing (ChIP-Seq) showed that this T372R substitution changes the DNA motif bound by YY1. Global analysis of gene expression demonstrated distinct clustering of tumors with and without YY1(T372R) mutations. Genes showing large increases in expression in YY1(T372R) tumors included ADCY1 (an adenylyl cyclase) and CACNA2D2 (a Ca(2+) channel); both are expressed at very low levels in normal β-cells and show mutation-specific YY1 binding sites. Both gene products are involved in key pathways regulating insulin secretion. Expression of these genes in rat INS-1 cells demonstrated markedly increased insulin secretion. These findings indicate that YY1(T372R) mutations are neomorphic, resulting in constitutive activation of cAMP and Ca(2+) signaling pathways involved in insulin secretion.
journal_name
Proc Natl Acad Sci U S Aauthors
Cromer MK,Choi M,Nelson-Williams C,Fonseca AL,Kunstman JW,Korah RM,Overton JD,Mane S,Kenney B,Malchoff CD,Stalberg P,Akerström G,Westin G,Hellman P,Carling T,Björklund P,Lifton RPdoi
10.1073/pnas.1503696112subject
Has Abstractpub_date
2015-03-31 00:00:00pages
4062-7issue
13eissn
0027-8424issn
1091-6490pii
1503696112journal_volume
112pub_type
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