Literature DB >> 8100767

Altered rhombomere-specific gene expression and hyoid bone differentiation in the mouse segmentation mutant, kreisler (kr).

M A Frohman1, G R Martin, S P Cordes, L P Halamek, G S Barsh.   

Abstract

Rhombomeres appear transiently in the vertebrate hindbrain shortly after neurulation and are thought to represent embryologic compartments in which the expression of different combinations of genes leads to segment-specific differentiation of the developing hindbrain, the cranial ganglia, and the branchial arches. To determine the extent to which gene expression is related to the formation of visible rhombomere boundaries, we have examined, by in situ hybridization, the expression of five rhombomere-specific genes in mouse embryos homozygous for the kreisler (kr) mutation, in which rhombomeres 4-7 are replaced by a smooth morphologically unsegmented neural tube. Using molecular probes specific for Hoxb-1 (Hox-2.9), Hoxb-3 (Hox-2.7), Hoxb-4 (Hox-2.6), Krox-20, or Fgf-3 (Int-2), we found that the kr mutation affects the expression of all the genes we examined, but, surprisingly, the altered patterns of expression are not restricted to that portion of the mutant hindbrain which is morphologically abnormal. Rostral expression boundaries of Hoxb-3 and Hoxb-4 are displaced from their normal positions at r4/5 and r6/7 to the approximate positions of r3/4 and r4/5, respectively. The expression domains of Krox-20 and Fgf-3 are also displaced in a rostral direction and the intensity of Fgf-3 hybridization is greatly reduced. The expression domain of Hoxb-1 is affected differently from the other genes in kr/kr embryos; its rostral boundary at r3/4 is intact but the caudal boundary is displaced from its normal location at r4/5 to the approximate position of r5/6. Because boundaries of gene expression for Hoxb-1 and Hoxb-4 are found in a region of the kr/kr hindbrain that lacks visible rhombomeres, establishment of regional identity, as reflected by differential gene expression, does not require overt segmentation. To investigate whether the altered patterns of gene expression we observed in the kr/kr embryonic hindbrain are associated with morphologic changes in the adult, we examined neural crest-derived tissues of the second and third branchial arches, which normally arise from rhombomeres 4 and 6, respectively. We found that the hyoid bone in kr/kr animals exhibited an accessory process on the greater horn (a third arch structure) most easily explained by ectopic development of a second arch structure (the hyoid lesser horn) in an area normally derived from the third arch.

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Year:  1993        PMID: 8100767     DOI: 10.1242/dev.117.3.925

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  20 in total

1.  Molecular genetics of pattern formation in the inner ear: do compartment boundaries play a role?

Authors:  J V Brigande; A E Kiernan; X Gao; L E Iten; D M Fekete
Journal:  Proc Natl Acad Sci U S A       Date:  2000-10-24       Impact factor: 11.205

2.  Krox20 and kreisler co-operate in the transcriptional control of segmental expression of Hoxb3 in the developing hindbrain.

Authors:  Miguel Manzanares; Jeannette Nardelli; Pascale Gilardi-Hebenstreit; Heather Marshall; François Giudicelli; María Teresa Martínez-Pastor; Robb Krumlauf; Patrick Charnay
Journal:  EMBO J       Date:  2002-02-01       Impact factor: 11.598

3.  PIASxbeta acts as an activator of Hoxb1 and is antagonized by Krox20 during hindbrain segmentation.

Authors:  Mario Garcia-Dominguez; Pascale Gilardi-Hebenstreit; Patrick Charnay
Journal:  EMBO J       Date:  2006-05-04       Impact factor: 11.598

Review 4.  The role of the hindbrain in patterning of the otocyst.

Authors:  Daniel Choo
Journal:  Dev Biol       Date:  2007-06-02       Impact factor: 3.582

5.  Krox20 controls the transcription of its various targets in the developing hindbrain according to multiple modes.

Authors:  Anne Desmazières; Patrick Charnay; Pascale Gilardi-Hebenstreit
Journal:  J Biol Chem       Date:  2009-02-13       Impact factor: 5.157

6.  Expression of Fgf-3 in relation to hindbrain segmentation, otic pit position and pharyngeal arch morphology in normal and retinoic acid-exposed mouse embryos.

Authors:  R Mahmood; I J Mason; G M Morriss-Kay
Journal:  Anat Embryol (Berl)       Date:  1996-07

7.  Differential expression of bone morphogenetic proteins in the developing vestibular and auditory sensory organs.

Authors:  S H Oh; R Johnson; D K Wu
Journal:  J Neurosci       Date:  1996-10-15       Impact factor: 6.167

8.  Rhombomere-specific analysis reveals the repertoire of genetic cues expressed across the developing hindbrain.

Authors:  David Chambers; Leigh Jane Wilson; Fabienne Alfonsi; Ewan Hunter; Uma Saxena; Eric Blanc; Andrew Lumsden
Journal:  Neural Dev       Date:  2009-02-10       Impact factor: 3.842

9.  Downstream genes of Pax6 revealed by comprehensive transcriptome profiling in the developing rat hindbrain.

Authors:  Keiko Numayama-Tsuruta; Yoko Arai; Masanori Takahashi; Makiko Sasaki-Hoshino; Nobuo Funatsu; Shun Nakamura; Noriko Osumi
Journal:  BMC Dev Biol       Date:  2010-01-18       Impact factor: 1.978

10.  FGF signaling controls caudal hindbrain specification through Ras-ERK1/2 pathway.

Authors:  Ferran Aragon; Cristina Pujades
Journal:  BMC Dev Biol       Date:  2009-12-03       Impact factor: 1.978

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