Genomics · 2006
A series of ENU-induced single-base substitutions in a long-range cis-element altering Sonic hedgehog expression in the developing mouse limb bud.
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Masuya Hiroshi, Sezutsu Hideki, Sakuraba Yoshiyuki, Sagai Tomoko, Hosoya Masaki, Kaneda Hideki, Miura Ikuo, Kobayashi Kimio, Sumiyama Kenta, Shimizu Aya, Nagano Junko, Yokoyama Haruka, Kaneko Satoko, Sakurai Noriko, Okagaki Yuka, Noda Tetsuo, Wakana Shigeharu, Gondo Yoichi, Shiroishi Toshihiko
Аннотация
Mammal-fish-conserved-sequence 1 (MFCS1) is a highly conserved sequence that acts as a limb-specific cis-acting regulator of Sonic hedgehog (Shh) expression, residing 1 Mb away from the Shh coding sequence in mouse. Using gene-driven screening of an ENU-mutagenized mouse archive, we obtained mice with three new point mutations in MFCS1: M101116, M101117, and M101192. Phenotype analysis revealed that M101116 mice exhibit preaxial polydactyly and ectopic Shh expression at the anterior margin of the limb buds like a previously identified mutant, M100081. In contrast, M101117 and M101192 show no marked abnormalities in limb morphology. Furthermore, transgenic analysis revealed that the M101116 and M100081 sequences drive ectopic reporter gene expression at the anterior margin of the limb bud, in addition to the normal posterior expression. Such ectopic expression was not observed in the embryos carrying a reporter transgene driven by M101117. These results suggest that M101116 and M100081 affect the negative regulatory activity of MFCS1, which suppresses anterior Shh expression in developing limb buds. Thus, this study shows that gene-driven screening for ENU-induced mutations is an effective approach for exploring the function of conserved, noncoding sequences and potential cis-regulatory elements.
Предметные рубрики MeSH
AnimalsBase SequenceConserved SequenceDNA PrimersEnhancer Elements, GeneticEthylnitrosoureaExtremitiesFemaleGene Expression Regulation, DevelopmentalGenes, RegulatorGenes, ReporterGenetic Complementation TestHedgehog ProteinsIn Situ HybridizationLimb Deformities, CongenitalMaleMiceMice, Inbred C57BLMice, Inbred DBAMice, Mutant StrainsMice, TransgenicPhenotypePoint MutationPolymorphism, Single NucleotidePregnancy