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We show that in middle-late meiosis the expression pattern is regulated primarily through the regulation of the NDT80 transcript levels.
Although it is not clearly elucidated, this cell growth pattern is regulated by the apical protein complex DivIVA.
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We demonstrated that the catalase activity pattern was regulated in different growth stages displaying the highest levels during the stationary phase.
Interestingly, we find that some genes previously thought to be expressed in a larval-specific, or sex-specific pattern are regulated more indirectly by the presence of germ cells, not by life stage or the sex determination hierarchy.
Changes of splicing pattern are regulated by trans-acting RNA-binding proteins that can be expressed in a temporal- or cell-type-specific manner to enhance or silence particular splicing events (Black, 2003; Matlin et al., 2005; Chen and Manley, 2009; Kalsotra and Cooper, 2011; Braunschweig et al., 2013; Kornblihtt et al., 2013).
Drosophila eggshell patterning is regulated by the epidermal growth factor receptor (EGFR) signaling pathway.
This suggests that the activity of the Nxnl1 promoter, like that of other genes that show highly cell-type restricted expression patterns, is regulated by transcription factors that are sensitive to the cellular context of the cell.
How this patterning is regulated by cells is not understood.
Normal fruit patterning is regulated by uORFs and requires RPL24-dependent translation reinitiation on certain uORF-containing mRNAs [ 25, 26].
Thus far, only a handful of genes have been shown to control the development of specific nephron segments of which none have been explicitly connected to an explanation for how patterning is regulated along the whole length of the nephron.
However, it is uncertain whether these color patterns are regulated by genetic factors.
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