Journal Article

Dominant-negative STAT5B mutations cause growth hormone insensitivity with short stature and mild immune dysregulation

Andrew, Shayne F., Neumann, David, Schwartz, I. David, Hwa, Vivian, Dattani, Mehul T., Colombo, Roberto, Gevers, Evelien F., Metherell, Louise A., Rockstroh, Denise, Kowalczyk, Julia, Sanchez, Marco A., Klammt, Jürgen, Rosenfeld, Ron G., Pfäffle, Roland, Dauber, Andrew, Vokurkova, Doris

2018

Overview

Growth hormone (GH) insensitivity syndrome (GHIS) is a rare clinical condition in which production of insulin-like growth factor 1 is blunted and, consequently, postnatal growth impaired. Autosomal-recessive mutations in signal transducer and activator of transcription (STAT5B), the key signal transducer for GH, cause severe GHIS with additional characteristics of immune and, often fatal, pulmonary complications. Here we report dominant-negative, inactivating STAT5B germline mutations in patients with growth failure, eczema, and elevated IgE but without severe immune and pulmonary problems. These STAT5B missense mutants are robustly tyrosine phosphorylated upon stimulation, but are unable to nuclear localize, or fail to bind canonical STAT5B DNA response elements. Importantly, each variant retains the ability to dimerize with wild-type STAT5B, disrupting the normal transcriptional functions of wild-type STAT5B. We conclude that these STAT5B variants exert dominant-negative effects through distinct pathomechanisms, manifesting in milder clinical GHIS with general sparing of the immune system. Severe growth hormone insensitivity syndrome (GHIS) with immunodeficiency is caused by autosomal recessive mutations in STAT5B. Here the authors report heterozygous STAT5B mutations with dominant-negative effects, causing mild GHIS without immune defects.

• Publisher: Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
• Subject: 13/109 / 13/51 / 14/19 / 38/23 / 38/88 / 45/71 / 631/80/86/2368 / 692/163/2743/1530 / 692/308/2056 / 82/80 / 96/21 / 96/95 / Adolescent / Cell Line / Child / Deoxyribonucleic acid / DNA / Eczema / Eczema - genetics / Female / Genetic Predisposition to Disease - genetics / Germ-Line Mutation - genetics / Growth hormones / HEK293 Cells / Human Growth Hormone - metabolism / Humanities and Social Sciences / Humans / Immune system / Immunoglobulin E / Immunoglobulin E - blood / Infant / Insulin / Insulin-Like Growth Factor I - biosynthesis / Laron Syndrome - genetics / Male / multidisciplinary / Mutation / Mutation, Missense - genetics / Physical growth / Regulatory sequences / Response Elements - genetics / Science / Science (multidisciplinary) / Skin diseases / STAT5 Transcription Factor - genetics / Transcription / Tyrosine