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Pudgy mouse rib deformities emanate from abnormal paravertebral longitudinal cartilage/bone accumulations
by
Wang, Jamie
, Flynn, Evelyn
, Wu, Joy Y.
, Shapiro, Frederic
in
abnormal rib formation
/ Animals
/ Cartilage
/ Embryo, Mammalian
/ Epigenomics
/ Intracellular Signaling Peptides and Proteins - genetics
/ Membrane Proteins - genetics
/ Mice
/ Mutation
/ paravertebral tissue accumulation
/ pudgy mouse
/ Receptors, Notch
/ Ribs - abnormalities
/ segmentation clock disorder
/ supramolecular structural changes
2024
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Pudgy mouse rib deformities emanate from abnormal paravertebral longitudinal cartilage/bone accumulations
by
Wang, Jamie
, Flynn, Evelyn
, Wu, Joy Y.
, Shapiro, Frederic
in
abnormal rib formation
/ Animals
/ Cartilage
/ Embryo, Mammalian
/ Epigenomics
/ Intracellular Signaling Peptides and Proteins - genetics
/ Membrane Proteins - genetics
/ Mice
/ Mutation
/ paravertebral tissue accumulation
/ pudgy mouse
/ Receptors, Notch
/ Ribs - abnormalities
/ segmentation clock disorder
/ supramolecular structural changes
2024
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Pudgy mouse rib deformities emanate from abnormal paravertebral longitudinal cartilage/bone accumulations
by
Wang, Jamie
, Flynn, Evelyn
, Wu, Joy Y.
, Shapiro, Frederic
in
abnormal rib formation
/ Animals
/ Cartilage
/ Embryo, Mammalian
/ Epigenomics
/ Intracellular Signaling Peptides and Proteins - genetics
/ Membrane Proteins - genetics
/ Mice
/ Mutation
/ paravertebral tissue accumulation
/ pudgy mouse
/ Receptors, Notch
/ Ribs - abnormalities
/ segmentation clock disorder
/ supramolecular structural changes
2024
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Pudgy mouse rib deformities emanate from abnormal paravertebral longitudinal cartilage/bone accumulations
Journal Article
Pudgy mouse rib deformities emanate from abnormal paravertebral longitudinal cartilage/bone accumulations
2024
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Overview
The pudgy (pu/pu) mouse, caused by a recessive mutation in the Notch family Delta like-3 gene (Dll3), has severe rib, vertebral body and intervertebral disc abnormalities. Using whole-mount preparations and serial histologic sections we demonstrate: 1) localized paravertebral longitudinal cartilage/bone accumulations (PVLC/BAs) invariably associated with branched, fused and asymmetrically spaced ribs that emanate from it laterally; 2) abnormal rib formation immediately adjacent to abnormal vertebral body and intervertebral disc formation in asymmetric right/left fashion; and 3) patterns of rib deformation that differ in each mouse. Normal BALB/c embryo and age-matched non-affected pu/+ mice assessments allow for pu/pu comparisons. The Dll3 Notch family gene is involved in normal somitogenesis via the segmentation clock mechanism. Although pathogenesis of rib deformation is initially triggered by the Dll3 gene mutation, these findings of abnormal asymmetric costo-vertebral region structure imply that differing patterns cannot be attributed to this single gene mutation alone. All findings implicate a dual mechanism of malformation: the Dll3 gene mutation leading to subtle timing differences in traveling oscillation waves of the segmentation clock and further subsequent misdirection of tissue formation by altered chemical reaction-diffusion and epigenetic landscape responses. PVLC/BAs appear as primary supramolecular structures underlying severe rib malformation associated both with time-sensitive segmentation clock mutations and subsequent reactions.
Publisher
The Company of Biologists Ltd,The Company of Biologists
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