1988
DOI: 10.1101/gad.2.12b.1736
|View full text |Cite
|
Sign up to set email alerts
|

Expression patterns of the homeo box-containing genes En-1 and En-2 and the proto-oncogene int-1 diverge during mouse development.

Abstract: We have compared the expression of the murine genes En-l,En-2, and int-1 during development by in situ hybridization. Expression of all three genes was first detected at 8.0 days in overlapping bands of the anterior neural folds. By 12.0 days the expression patterns diverged. En-1 and En-2 were expressed in a similar ring of cells in the central nervous system (CNS) at the midbrain/hindbrain junction. En-1 was also expressed de novo in two lateral stripes extending the length of the hindbrain and spinal cord, … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

6
166
0
2

Year Published

1994
1994
2014
2014

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 365 publications
(174 citation statements)
references
References 23 publications
(34 reference statements)
6
166
0
2
Order By: Relevance
“…It is interesting in this context to note that a defective serotonergic innervation is also compatible with alterations of brainstem segmentation genes such as engrailed or Hox 2, which have been implicated in autism (Polleux and Lauder, 2004;Bartlett et al, 2005;Benayed et al, 2005). Serotonergic projection neurons develop in the brainstem areas under control of these segmentation genes (Davis and Joyner, 1988;Gavalas et al, 2003). Yet, serotonergic afferents only innervate cortex just before birth and thus begin to exert their effects on cortical maturation predominantly after birth in both rodent and human (Lidov and Molliver, 1982;Dori et al, 1996;Connell et al, 2004).…”
Section: Neonatal Serotonin Depletions As An Animal Model For Autismmentioning
confidence: 96%
“…It is interesting in this context to note that a defective serotonergic innervation is also compatible with alterations of brainstem segmentation genes such as engrailed or Hox 2, which have been implicated in autism (Polleux and Lauder, 2004;Bartlett et al, 2005;Benayed et al, 2005). Serotonergic projection neurons develop in the brainstem areas under control of these segmentation genes (Davis and Joyner, 1988;Gavalas et al, 2003). Yet, serotonergic afferents only innervate cortex just before birth and thus begin to exert their effects on cortical maturation predominantly after birth in both rodent and human (Lidov and Molliver, 1982;Dori et al, 1996;Connell et al, 2004).…”
Section: Neonatal Serotonin Depletions As An Animal Model For Autismmentioning
confidence: 96%
“…The largest class of homeobox genes, the Hox genes, are expressed in a region posterior to the midbrain where they are thought to confer regional identity on specific fields of cells (review in Deschamps and Meijlink, 1992;McGinnis and Krumlauf, 1992). Likewise, en-1 and en-2 are not expressed anterior of the midbrain (Davis and Joyner, 1988), and are known to be involved in midbrain and hindbrain development (Joyner et al, 1991). Genes of the Pax family, on the other hand, are expressed along the entire longitudinal axis of the neural tube (for review, see Deutsch and Gruss, 1991).…”
Section: Ziml Expression In the Developing Central Nervous Systemmentioning
confidence: 99%
“…A null mutation of En1 results in the absence of most of the cerebellum and midbrain, and in lethality shortly after birth [66]. En2 expression is also found at the presumptive midbrain-hindbrain region but initiates later, at the 5 somite stage [25,26]. Unlike En1, null alleles of Engrailed-2 have only a subtle neurological phenotype.…”
Section: Introductionmentioning
confidence: 99%