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Molecular and Cellular Biology, August 2001, p. 5658-5666, Vol. 21, No. 16
Institute of Child Health, London WCIN
1EH,1 and MRC Laboratory of Molecular
Biology, Cambridge CB2 2QH,2 United Kingdom
Received 7 February 2001/Returned for modification 2 April
2001/Accepted 23 May 2001
The MTG8 (ETO) locus is involved in a
reciprocal exchange with runx1 in the t(8;21) of acute
myeloid leukemia. It is a member of a small gene family encoding
transcriptional regulators that interact with corepressors and histone
deacetylase. However, the physiologic cellular processes controlled by
MTG8 are not known. In order to gain an insight into the
latter, we have generated mutant mice with an insertional inactivation
at the locus, which disrupts transcription of exon 2. The postnatal
viability of homozygous mutants was greatly reduced. In approximately
25% the midgut was missing, whereas practically all pups surviving
past the first 2 days showed severe growth impairment, which was likely
due to a gross disruption of the gut architecture. The latter phenotype could be traced back to late embryonic development. No difference in
gut cell differentiation or proliferation was found compared to
wild-type littermates. Levels of factors known to be involved in gut
morphogenesis were also unchanged. MTG8 is expressed in the
outermost layers of the developing gut from at least E9.5. Thus,
MTG8 plays a novel, essential role in the gastrointestinal system.
0270-7306/01/$04.00+0 DOI: 10.1128/MCB.21.16.5658-5666.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Gene Targeting Reveals a Crucial Role for
MTG8 in the Gut
*
Corresponding author. Mailing address: Developmental
Biology Unit, The Institute of Child Health, 30 Guilford St., London WCIN 1EH, United Kingdom. Phone: 44-20-7813-8492. Fax:
44-20-7831-4366. E-mail:
fcalabi{at}hgmp.mrc.ac.uk.
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