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Replication fork stalling may occur in regions that contain clustered ribonucleotides, as seen at the S. pombe mating switch locus (Vengrova and Dalgaard, 2006).
First, a diribonucleotide at the S. pombe mating switch locus is believed to be the signal initiating homologous recombination (Vengrova and Dalgaard, 2004).
Replication fork arrest is also used to control the direction of replication through a site in the mating locus that carries an imprint that controls which daughter cell will undergo a mating switch event (Dalgaard and Klar 2001).
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Mate switching between broods is uncommon, with pairs staying together over several years.
Female crest length is the primary factor of male mate switching between years.
Mate switching can, however, occur for example when male or female dies accidentally during the early breeding season.
Since mate switching within a breeding season has never been visually observed in this species (see [5], [7]), EPPs and QPs predominantly result from extrapair copulations.
However, a close examination of these studies revealed that unequivocal evidence for QP is slim due to possibility of rapid mate-switching and/or insufficient molecular work [4].
A comparable phenomenon has been previously observed in the monogamous long-tailed tit, Aegithalos caudatus, where optimal outbreeding provided a better explanation than the "forced divorce" hypothesis to patterns of mate-switching [26].
Unlike cross-fostering studies, our ability to separate nest effects (i.e., the effect of common environment) from genetic effects depends on the extent of extra-pair paternity and mate-switching across different reproductive episodes.
To ascertain the relationship among the different births by the same male, we used the same body size of females to decrease the probability of the size-biased sexual selection and mate switching (Naud et al., 2009; Hunt et al., 2009; Paczolt and Jones, 2010).
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