Maternally derived transcripts: identification and characterisation during oocyte maturation and early cleavage

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dc.contributor Cui, Xiang-Shun
dc.contributor Kim, Nam-Hyung
dc.date.accessioned 2012-01-30T02:28:41Z
dc.date.available 2012-01-30T02:28:41Z
dc.date.issued 2007
dc.identifier.citation Rep. Fert. Dev. (2007) 19(1): 25-34
dc.identifier.issn 1031-3613
dc.identifier.uri http://livestocklibrary.com.au/handle/1234/15371
dc.description.abstract The identification and characterisation of differentially regulated genes in oocytes and early embryos are required to understand the mechanisms involved in maturation, fertilisation, early cleavage and even long-term development. Several methods, including reverse transcription?polymerase chain reaction-based suppression subtractive hybridisation, differential display and cDNA microarray, have been applied to identify maternally derived genes in mammalian oocytes. However, conventional gene-knockout experiments to determine specific gene functions are labour intensive and inefficient. Recent developments include the use of RNA interference techniques to establish specific gene functions in mammalian oocytes and early embryos. Regulation of the poly(A) tail length is a major factor in controlling the activities of maternal transcripts in mammals. Further studies are required to clarify the mechanisms by which expression levels of maternally derived transcripts are regulated. In the present review, we focus on the identification and functions of the differentially expressed transcripts during oocyte maturation, fertilisation and early cleavage.
dc.publisher CSIRO Publishing
dc.source.uri http://www.publish.csiro.au/?act=view_file&file_id=RD06128.pdf
dc.subject gene expression
dc.subject maternal genes
dc.title Maternally derived transcripts: identification and characterisation during oocyte maturation and early cleavage
dc.type Research
dc.description.version Journal article|Conference paper
dc.identifier.volume 19
dc.identifier.page 25-34
dc.identifier.issue 1


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