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Hmga1/Hmga2 double knock-out mice display a “superpygmy” phenotype
Author(s) -
Antonella Federico,
Floriana Forzati,
Francesco Esposito,
Claudio Arra,
Giuseppe Palma,
Antônio Barbieri,
Dario Palmieri,
Monica Fedele,
Giovanna Maria Pierantoni,
Ivana De Martino,
Alfredo Fusco
Publication year - 2014
Publication title -
biology open
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.936
H-Index - 41
ISSN - 2046-6390
DOI - 10.1242/bio.20146759
Subject(s) - biology , hmga2 , phenotype , gene , genetics , microbiology and biotechnology , cancer research , microrna
The HMGA1 and HMGA2 genes code for proteins belonging to the High Mobility Group A family. Several genes are negatively or positively regulated by both these proteins, but a number of genes are specifically regulated by only one of them. Indeed, knock-out of the Hmga1 and Hmga2 genes leads to different phenotypes: cardiac hypertrophy and type 2 diabetes in the former case, and a large reduction in body size and amount of fat tissue in the latter case. Therefore, to better elucidate the functions of the Hmga genes, we crossed Hmga1-null mice with mice null for Hmga2. The Hmga1(-/-)/Hmga2(-/-) mice showed reduced vitality and a very small size (75% smaller than the wild-type mice); they were even smaller than pygmy Hmga2-null mice. The drastic reduction in E2F1 activity, and consequently in the expression of the E2F-dependent genes involved in cell cycle regulation, likely accounts for some phenotypic features of the Hmga1(-/-)/Hmga2(-/-) mice.

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