Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
1999-7-8
pubmed:abstractText
The closely related Hox transcription factors Ultrabithorax (Ubx) and Antennapedia (Antp) respectively direct first abdominal (A1) and second thoracic (T2) segment identities in Drosophila. It has been proposed that their functional differences derive from their differential occupancy of DNA target sites. Here we show that a hybrid version of Ubx (Ubx-VP16), which possesses an enhanced transcriptional activation function, no longer directs A1 denticle pattern in embryonic epidermal cells. Instead, it mimics Antp in directing T2 denticle pattern, and it can rescue the cuticular loss-of-function phenotype of Antp mutants. In cells that do not produce denticles, Ubx-VP16 appears to have largely retained its normal repressive regulatory functions. These results suggest that the modulation of Hox activation and repression functions can account for segment-specific morphological differences that are controlled by different members of the Hox family. Our results also are consistent with the idea that activity regulation underlies the phenotypic suppression phenomenon in which a more posterior Hox protein suppresses the function of a more anterior member of the Hox cluster. The acquisition of novel activation and repression potentials in Hox proteins may be an important mechanism underlying the generation of subtle morphological differences during evolution.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-1346368, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-1350559, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-1358457, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-1680563, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-1968232, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-1970762, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-2105847, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-2567632, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-2843426, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-7555708, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-7630416, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-7637779, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-7859741, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-7900989, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-7903298, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-7906203, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-7906390, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-7907545, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-7913879, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-7914367, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-7914870, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-7925003, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-8098307, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-8101003, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-8223268, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-8577843, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-8625844, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-8857539, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-9155029, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-9171376, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-9409661, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-9751061, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-9811579, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359793-9878063
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0027-8424
pubmed:author
pubmed:issnType
Print
pubmed:day
8
pubmed:volume
96
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
6802-7
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed:year
1999
pubmed:articleTitle
Activity regulation of Hox proteins, a mechanism for altering functional specificity in development and evolution.
pubmed:affiliation
Department of Biology, University of California at San Diego, La Jolla, CA 92093, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.