1987
DOI: 10.1128/mcb.7.4.1545
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Restriction of P-element insertions at the Notch locus of Drosophila melanogaster.

Abstract: P elements move about the Drosophila melanogaster genome in a nonrandom fashion, preferring some chromosomal targets for insertion over others (J. C. J. Eeken 77:6042-6046, 1980). Some of this specificity may be due to recognition of a particular DNA sequence in the target DNA; derivatives of an 8-base-pair consensus sequence are occupied by these transposable elements at many different chromosomal locations (K. O'Hare and G. M. Rubin, Cell 34:25-36, 1983). An additional level of specificity of P-element in… Show more

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Cited by 60 publications
(34 citation statements)
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References 23 publications
(36 reference statements)
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“…An apparent preference for insertion near 5' ends of genes had been noted previously for several specific genes (29,30), but excep-Disrupting tions were also known. Fig.…”
Section: P Elements Preferentially Mutate 5' Gene Regionssupporting
confidence: 56%
“…An apparent preference for insertion near 5' ends of genes had been noted previously for several specific genes (29,30), but excep-Disrupting tions were also known. Fig.…”
Section: P Elements Preferentially Mutate 5' Gene Regionssupporting
confidence: 56%
“…Hence, in most cases, the P-lacZ fusion can come under the control of Drosophila expression elements without causing major disruption to the structure or expression of an adjacent essential gene. Other workers have reported a preference of P elements for genomic targets in promoter regions, and some such insertions appear to alter the level or pattern of expression of the downstream transcript without abolishing it (20,21). Thus, many P insertions near promoters and in intergenic regions may bring the P-lacZ fusion under the control of at least some of the elements regulating expression of one or more adjacent Drosophila genes without giving a lethal phenotype.…”
Section: Resultsmentioning
confidence: 99%
“…An earlier report analyzed 13 hybrid-dysgenesis-induced N mutations. 21 Like N nd-p , all of the mutations were P element insertions in the first exon, upstream of the start of translation. Twelve of the mutations were recessive lethals, indicative of a large reduction in N expression and one was a recessive, hypomorphic, notchoidlike mutation similar in phenotype to N nd-p .…”
mentioning
confidence: 99%