Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/8481
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Type: Journal article
Title: Reproductive performance in female ClockΔ19 mutant mice
Other Titles: Reproductive performance in female ClockDelta19 mutant mice
Author: Kennaway, D.
Boden, M.
Voultsios, A.
Citation: Reproduction Fertility and Development, 2004; 16(8):801-810
Publisher: C S I R O Publishing
Issue Date: 2004
ISSN: 1031-3613
1448-5990
Statement of
Responsibility: 
David J. Kennaway, Michael J. Boden and Athena Voultsios
Abstract: The relationship between circadian rhythmicity and rodent reproductive cyclicity is well established, but the impact of disrupted clock gene function on reproduction has not been well established. The present study evaluated the reproductive performance of mice carrying the ClockΔ19 mutation that were either melatonin deficient (ClockΔ19/Δ19) or had the capacity to synthesise melatonin reinstated (ClockΔ19/Δ19+MEL). The ClockΔ19/Δ19 mice took 2–3 days longer to mate, and to subsequently deliver pups, than their control line. The melatonin-competent mutants had a smaller, but still significant (P < 0.05), delay. The ClockΔ19 mutation resulted in smaller median litter sizes compared with control lines (seven v. eight pups; P < 0.05), whereas melatonin proficiency reversed this difference. Survival to weaning was 84% and 80% for the ClockΔ19/Δ19 and ClockΔ19/Δ19+MEL lines, respectively, compared with 94–96% for the two control lines. The ClockΔ19/Δ19 mutants became behaviourally arrhythmic in constant darkness but, despite this, seven of seven became pregnant when paired with males after at least 14 days of constant darkness (five of seven within 4 days of pairing). In the ClockΔ19/Δ19+MEL mice, seven of 15 became arrhythmic in constant darkness but still became pregnant. The seven mice that free ran for at least 14 days in constant darkness with a period of 27.1 h also became pregnant. The present study has demonstrated that the ClockΔ19 mutation has significant, but subtle, effects on reproductive performance. The reintroduction of melatonin competency and/or other genes as a result of crosses with CBA mice reduced the impact of the mutation further. It would appear that redundancy in genes in the circadian system allows the reproductive cyclicity to persist in mice, albeit at a suboptimal level.
Keywords: Animals; Mice; Mice, Mutant Strains; Trans-Activators; Sequence Deletion; Circadian Rhythm; Reproduction; Fertility; Mutation; Darkness; Female; CLOCK Proteins
Rights: © CSIRO 2004
RMID: 0020041335
DOI: 10.1071/RD04023
Appears in Collections:Obstetrics and Gynaecology publications

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