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Growth, Differentiation and Sexuality

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300 R. Debuchy <strong>and</strong> B.G. Turgeon<br />

Fig. 15.3. Comparative organization of the MAT locus in<br />

eight Euascomycete species. Analyses are reported for P.<br />

anserina (LG I, supercontig G, 69,500 to 92,000), C. globosum<br />

(LG not determined, supercontig 1.3, bases 3,980,000 to<br />

4,001,000 <strong>and</strong> supercontig 1.2, bases 4,630,000 to 4,665,000),<br />

N. crassa (LG I, contig 3.86 <strong>and</strong> 3.87), G. zeae (LG not determined,<br />

contig 1.359 <strong>and</strong> 1.358), M. grisea (LG III, contig<br />

2.596, 2.597 <strong>and</strong> 2.600), <strong>and</strong> E. nidulans (LG VI, contig 1.49<br />

<strong>and</strong> LG III, contig 1.80). Gene positions are indicated by<br />

arrowed boxes with gene name inside. Below each box is<br />

the gene number, asreferredtobythesequencingproject,<br />

when available. For C. globosum, the number under the box<br />

indicates the percentage of identity at the amino-acid level<br />

with the P. anserina putative homolog. Arrowed boxes with<br />

thick lines indicate C. globosum genes that have no P. anserina<br />

counterparts. Distances <strong>and</strong> gene sizes are not to scale;<br />

large genome sequences containing genes not relevant to<br />

the comparison have been omitted, <strong>and</strong> are symbolized by<br />

breaks in the line between genes. The number of genes<br />

present in the break can be inferred from the gene number<br />

adjacent to the break. Gene names refer to the GenBank<br />

name or to a gene encoding a protein showing best similaritytotheputativegeneproductfollowingBlastpanalysis<br />

(Altschul et al. 1997). When no significant similarity was<br />

found, but a conserved domain was found, this domain was<br />

used for identifying the gene. Gene products with no similarity<br />

in Swissprot, nor with any identified domain, are in-<br />

dicatedashypotheticalprotein(hyp. prot.). Aa_trans Transmembrane<br />

amino-acid transporter domain, APC5 similar<br />

to anaphase promoting factor component 5 of S. pombe<br />

(accession no. Q9P4W7), ATG3 similar to autophagocytosis<br />

protein of S. cerevisiae (accession no. P40344), ATPase<br />

cation transport ATPase domain, BGL1 beta glucosidase<br />

homolog (accession number AAB82946.1), cox13 similar to<br />

cytochrome c oxydase polypeptide VIa, mitochondrial precursor,<br />

of S. pombe (accession no. O74471), CWF24 similar<br />

to cell cycle control protein of S. pombe (accession number<br />

Q9P6R8), APN2 similar to DNA (apurinic <strong>and</strong> apyrimidinic<br />

site) lyase 2 of S. cerevisiae (accession no. P38207),<br />

GAP1 GTPase activating protein homolog (accession no.<br />

AAB82943.1), HMG high-mobility-group domain, endo exo<br />

endo_exo_phos domain, ORF1 similar to S. cerevisiae ORF<br />

YLR456W (accession no. U22383), palI similar to palI of<br />

E. nidulans (accession no. CAA07588), P450 similar to trichodiene<br />

oxygenase of Fusarium sporotrichioides (accession<br />

no. Q12612), PKS similar to conidial yellow pigment<br />

biosynthesis polyketide synthase of E. nidulans (accession<br />

no. Q03149), SLA2 similar to SLA2 transmembrane protein<br />

of S. cerevisae (accession no. P33338), S/T kinase similar to<br />

serine/threonine protein kinase involved in the regulation<br />

of DNA repair in S. pombe (accession no. P40235), SYG1 similar<br />

to SYG1 protein of S. cerevisiae (accession no. P40528),<br />

Tf2p similar to retrotransposable element TF2p 155-kDa<br />

protein type1 of S. pombe (accession no. Q05654)

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