دورية أكاديمية

A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant.

التفاصيل البيبلوغرافية
العنوان: A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant.
المؤلفون: Sidow, A, Bulotsky, M S, Kerrebrock, A W, Birren, B W, Altshuler, D, Jaenisch, R, Johnson, K R, Lander, E S
المصدر: Faculty Research 1990 - 1999
بيانات النشر: The Mouseion at the JAXlibrary
سنة النشر: 1999
المجموعة: The Jackson Laboratory: The Mouseion at the JAXlibrary
مصطلحات موضوعية: Animal, Base-Sequence, Chromosome-Mapping, Extremities, Heterozygote, Human, Limb-Deformities-Congenital, Mesoderm, Mice, Mice-Inbred-BALB-C, Models-Genetic, Molecular-Sequence-Data, Multigene-Family, Mutation, Proteins, Sequence-Homology-Amino-Acid, Time-Factors, Tissue-Distribution
الوصف: Early outgrowth of the vertebrate embryonic limb requires signalling by the apical ectodermal ridge (AER) to the progress zone (PZ), which in response proliferates and lays down the pattern of the presumptive limb in a proximal to distal progression. Signals from the PZ maintain the AER until the anlagen for the distal phalanges have been formed. The semidominant mouse mutant dactylaplasia (Dac) disrupts the maintenance of the AER, leading to truncation of distal structures of the developing footplate, or autopod. Adult Dac homozygotes thus lack hands and feet except for malformed single digits, whereas heterozygotes lack phalanges of the three middle digits. Dac resembles the human autosomal dominant split hand/foot malformation (SHFM) diseases. One of these, SHFM3 maps to chromosome 10q24 (Refs 6,7), which is syntenic to the Dac region on chromosome 19, and may disrupt the orthologue of Dac. We report here the positional cloning of Dac and show that it belongs to the F-box/WD40 gene family, which encodes adapters that target specific proteins for destruction by presenting them to the ubiquitination machinery. In conjuction with recent biochemical studies, this report demonstrates the importance of this gene family in vertebrate embryonic development.
نوع الوثيقة: text
اللغة: unknown
العلاقة: https://mouseion.jax.org/stfb1990_1999/1308Test
الإتاحة: https://mouseion.jax.org/stfb1990_1999/1308Test
رقم الانضمام: edsbas.AB59DD4B
قاعدة البيانات: BASE