A rare complex DNA rearrangement in the murine Steel gene results in exon duplication and a lethal phenotype

Saurabh Chandra, Reuben Kapur, Nadia Chuzhanova, Victoria Summey, David Prentice, Jane Barker, David N. Cooper, David A. Williams

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Kit ligand (Kitl), encoded by the Steel (Sl) locus, plays an essential role in hematopoiesis, gametogenesis, and melanogenesis during both embryonic and adult life. We have characterized a new spontaneous mutant of the Sl locus in mice designated KitlSl-20J that arose in the breeding colony at Jackson Laboratories. Heterozygous KitlSl-20J mice display a white belly spot and intercrossing results in an embryonic lethal phenotype in the homozygous state. Analysis of homozygous embryos demonstrated a significant reduction in fetal liver cellularity, colony forming unit-erythroid (CFU-E) progenitors, and a total absence of germ cells. Although expressed in vivo, recombinant mutant protein demonstrated loss of bioactivity that was correlated with lack of receptor binding. Analysis of the Sl gene transcripts in heterozygous KitlSl-20J mice revealed an in-frame tandem duplication of exon 3. A long-range polymerase chain reaction (PCR) strategy using overlapping primers in exon 3 amplified an approximately 7-kilobase (kb) product from DNA isolated from heterozygous KitlSl-20J mice but not from wild-type DNA that contained sequences from both introns 2 and 3 and an inverted intron 2 sequence, suggesting a complex rearrangement as the mechanism of the mutation. "Complexity analysis" of the sequence of the amplified product strongly suggests that local DNA motifs may have contributed to the generation of this spontaneous KitlSl-20J allele, likely mediated by a 2-step process. The KitlSl-20J mutation is a unique KitlSl allele and represents an unusual mechanism of mutation.

Original languageEnglish (US)
Pages (from-to)3548-3555
Number of pages8
JournalBlood
Volume102
Issue number10
DOIs
StatePublished - Nov 15 2003
Externally publishedYes

Fingerprint

Gene Rearrangement
Steel
Exons
Genes
Phenotype
Introns
DNA
Mutation
Recombinant proteins
Stem Cell Factor
Polymerase chain reaction
Alleles
Multifetal Pregnancy Reduction
Mutant Proteins
Bioactivity
Gametogenesis
Liver
Erythroid Precursor Cells
Nucleotide Motifs
Hematopoiesis

ASJC Scopus subject areas

  • Hematology

Cite this

Chandra, S., Kapur, R., Chuzhanova, N., Summey, V., Prentice, D., Barker, J., ... Williams, D. A. (2003). A rare complex DNA rearrangement in the murine Steel gene results in exon duplication and a lethal phenotype. Blood, 102(10), 3548-3555. https://doi.org/10.1182/blood-2003-05-1468

A rare complex DNA rearrangement in the murine Steel gene results in exon duplication and a lethal phenotype. / Chandra, Saurabh; Kapur, Reuben; Chuzhanova, Nadia; Summey, Victoria; Prentice, David; Barker, Jane; Cooper, David N.; Williams, David A.

In: Blood, Vol. 102, No. 10, 15.11.2003, p. 3548-3555.

Research output: Contribution to journalArticle

Chandra, S, Kapur, R, Chuzhanova, N, Summey, V, Prentice, D, Barker, J, Cooper, DN & Williams, DA 2003, 'A rare complex DNA rearrangement in the murine Steel gene results in exon duplication and a lethal phenotype', Blood, vol. 102, no. 10, pp. 3548-3555. https://doi.org/10.1182/blood-2003-05-1468
Chandra, Saurabh ; Kapur, Reuben ; Chuzhanova, Nadia ; Summey, Victoria ; Prentice, David ; Barker, Jane ; Cooper, David N. ; Williams, David A. / A rare complex DNA rearrangement in the murine Steel gene results in exon duplication and a lethal phenotype. In: Blood. 2003 ; Vol. 102, No. 10. pp. 3548-3555.
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