Drosophila Oogenesis: Methods and Protocols by Diana P. Bratu, Gerard P. McNeil

By Diana P. Bratu, Gerard P. McNeil

This quantity presents present updated protocols for getting ready the ovary for varied imaging concepts, genetic protocols for producing mutant clones, mosaic research and assessing cellphone dying. Chapters handle equipment for appearing genome huge gene expression research and bioinformatics for reports of RNA-protein interactions. Written within the hugely profitable Methods in Molecular Biology series layout, chapters comprise introductions to their respective subject matters, lists of the required fabrics and reagents, step by step, without difficulty reproducible laboratory protocols, and tips about troubleshooting and fending off identified pitfalls.

Authoritative and state of the art, Drosophila Oogenesis: tools and Protocols goals to make sure winning ends up in the extra examine of this important field.

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104. 105. 106. 107. 108. 109. 110. 111. 19 regulatory activity in the imaginal discs of Drosophila melanogaster. Cell Rep 2: 1014–1024 Manning L, Heckscher ES, Purice MD et al (2012) A resource for manipulating gene expression and analyzing cis-regulatory modules in the Drosophila CNS. Cell Rep 2:1002–1013 Pfeiffer BD, Jenett A, Hammonds AS et al (2008) Tools for neuroanatomy and neurogenetics in Drosophila. Proc Natl Acad Sci U S A 105:9715–9720 Jenett A, Rubin GM, Ngo TT et al (2012) A GAL4-Driver line resource for Drosophila neurobiology.

Thus, an embryo can be genetically homozygous for a given mutation, but the consequences of this mutation can be masked during the early stages of embryonic development by the presence of wild type mRNAs of the same gene deposited by the mother during oogenesis. To remove this “maternal contribution,” the wild type copies of the gene need to be removed in the germline of the mother during the formation of the egg. This can be achieved by inducing mitotic recombination in the mother’s germline stem cells which are the progenitors of all germ cells [28].

Vials may also be used instead of bottles. 10. Make sure there is no remaining food or yeast made available to the flies. Wet the Kimwipe with a few drops of H2O until it is damp. 11. Cut the tip off of a 200 μl pipette tip to widen the opening. Gently pipet the ovaries up and down in the tip in the depression slide. This will help to dislodge the later stage egg chambers from the ovaries. Pipet several times, then examine the Dissection and Isolation of Ovarian Tissue 27 ovaries in the dissecting microscope.

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