Gene dosage affects the cardiac and brain phenotype in nonmuscle myosin II-B–depleted mice
Deniz Üren, … , Yvette A. Preston, Robert S. Adelstein
Deniz Üren, … , Yvette A. Preston, Robert S. Adelstein
Published March 1, 2000
Citation Information: J Clin Invest. 2000;105(5):663-671. https://doi.org/10.1172/JCI8199.
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Article

Gene dosage affects the cardiac and brain phenotype in nonmuscle myosin II-B–depleted mice

Abstract

Complete ablation of nonmuscle myosin heavy chain II-B (NMHC-B) in mice resulted in cardiac and brain defects that were lethal during embryonic development or on the day of birth. In this paper, we report on the generation of mice with decreased amounts of NMHC-B. First, we generated BΔI/BΔI mice by replacing a neural-specific alternative exon with the PGK-Neo cassette. This resulted in decreased amounts of NMHC-B in all tissues, including a decrease of 88% in the heart and 65% in the brain compared with B+/B+ tissues. BΔI/BΔI mice developed cardiac myocyte hypertrophy between 7 months and 11 months of age, at which time they reexpressed the cardiac β-MHC. Serial sections of BΔI/BΔI brains showed abnormalities in neural cell migration and adhesion in the ventricular wall. Crossing BΔI/BΔI with B+/B– mice generated BΔI/B– mice, which showed a further decrease of approximately 55% in NMHC-B in the heart and brain compared with BΔI/BΔI mice. Five of 8 BΔI/B– mice were born with a membranous ventricular septal defect. Moreover, 5 of 5 BΔI/B– mice developed myocyte hypertrophy by 1 month; BΔI/B– mice also reexpressed the cardiac β-MHC. More than 60% of BΔI/B– mice developed overt hydrocephalus and showed more severe defects in neural cell migration and adhesion than did BΔI/BΔI mice. These data on BΔI/BΔI and BΔI/B– mice demonstrate a gene dosage effect of the amount of NMHC-B on the severity and time of onset of the defects in the heart and brain.

Authors

Deniz Üren, Hweung-Kon Hwang, Yoshinobu Hara, Kazuyo Takeda, Sachiyo Kawamoto, Antonella N. Tullio, Zu-Xi Yu, Victor J. Ferrans, Nancy Tresser, Alexander Grinberg, Yvette A. Preston, Robert S. Adelstein

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Brain defects in BΔΙ/B– mice at P0. (a–d) Low-magnification view of coro...
Brain defects in BΔΙ/B– mice at P0. (a–d) Low-magnification view of coronal sections from anterior to posterior. The lateral ventricles are expanded and the ventricular and subventricular structures of the cerebral cortex are destroyed (a–c), but the fourth ventricle is not expanded (d). The choroidal plexus looks normal (a, b, and d). (e) Enlargement of the boxed area shown in c showing stenosis and deformity of the cerebral aqueduct and the asymmetric development of the neuroepithelial cells. (f) Enlargement of the boxed area shown in d, showing loss of ependymal cells and the abnormal protrusion of a mass of cells containing large neurons into the fourth ventricle. The misplaced large neurons (arrows) are present in abundance. The ependymal cell layer is indicated (arrowhead). H&E stain.