Detection of Sad genes in various species of Neurospora

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Detection of Sad genes in various species of Neurospora

Please use this identifier to cite or link to this item: http://hdl.handle.net/10355/2205

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Title: Detection of Sad genes in various species of Neurospora
Author: Singh, Ashwin; Morris, Ryan; Shiu, Patrick
Contributor: University of Missouri-Columbia. Office of Undergraduate Research
Keywords: Neurospora
sad-1 genes
sad-2 genes
meiotic silencing by unpaired DNA
Date: 2005
Publisher: University of Missouri--Columbia. Office of Undergraduate Research
Abstract: Neurospora crassa is a haploid fungus that reproduces asexually during vegetative growth. However, in a nitrogen deficient environment, the two mating-type cells, A and a, can fuse together and enter the sexual cycle. During this transient diploid stage, a post-transcriptional gene silencing (PTGS) mechanism silences the expression of any unpaired gene. This mechanism is called meiotic silencing by unpaired DNA (MSUD) (Shiu, et al., 2001; Cell 107: 905-916). MSUD occurs when a gene is not paired with a homologue during meiosis. The unpaired DNA segment generates a sequence-specific signal, causing any paired or unpaired copies of that gene to be silenced. Two required genes for meiotic silencing have been identified; sad-1 encodes an RNA-directed RNA polymerase while sad-2 encodes a novel protein. Interspecific crosses between N. crassa and other related species are known to be infertile. This infertility may be due rearrangements caused by inversion and/or translocation. These could disrupt the pairings of genes needed for meiosis and ascus development, causing these genes to be silenced, resulting in sterility. This hypothesis is validated by observing that interspecific crosses within the genus Neurospora become much more fertile when the N. crassa parent contains a Sad-1 mutation. If MSUD is in other Neurospora species, it may represent another mechanism for speciation. This research project focuses to determine whether sad-1 and sad-2 are conserved in related species of Neurospora. Homologues of the sad genes were amplified in several fungal isolates by PCR (Polymerase Chain Reaction), using primers designed for those sequences. We have discovered that sad-1 and sad-2 can be found in several different Neurospora species; sad-1 is present in N. sitophila, N. tetrasperma, N. dodgei, N. galapagosensis, and N. africana, while sad-2 is found in N. sitophila, N. tetrasperma, and N. intermedia. The presence of sad genes in these species suggests MSUD may contribute to their reproductive isolation.
URI: http://hdl.handle.net/10355/2205

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