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Growth, Differentiation and Sexuality

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Mating Types in Euascomycetes 305<br />

Table. 15.3. Genome position of the homologs to C. heterostrophus <strong>and</strong> M. graminicola MAT flanking genes in Sordariomycetes<br />

<strong>and</strong> Eurotiomycetes<br />

GAP1 ORF1 MAT BGL1 pal1<br />

P. anserina<br />

LG I I I II I<br />

Supercontig E E G A F<br />

Start 280,606 402,224 79,454 3,309,367 432,338<br />

Stop<br />

C. globosum<br />

283,019 401,468 78,144 3,306,572 430,110<br />

Supercontig 1.3 1.3 1.3 (MAT1-1) 1.3<br />

Start 2,900,141 2,736,033 3,990,896 3,892,526<br />

Stop 2,902,311 2,736,841 3,991,867 3,894,742<br />

Supercontig 1.2 (MAT1-2) 1.2<br />

Start 4,650,124 4,159,504<br />

Stop<br />

N. crassa<br />

4,651,264 4,161,935<br />

LG I I I V I<br />

Supercontig 2 2 5 11 5<br />

Contig 3.22 3.23 3.86 3.199 3.88<br />

Gene number<br />

G. zeae<br />

NCU00553.1 NCU00590.1 NCU1960.1 NCU3641.1 NCU1996.1<br />

Supercontig 5 5 5 2 5<br />

Contig 1.348 1.349 1.358 1.160 1.353<br />

Gene number<br />

M. grisea<br />

FG08638.1 FG08689.1 FG08893.1 FG03570.1 FG08708.1<br />

LG VII VII VII I I<br />

Supercontig 4 33 4 2 2<br />

Contig 2.611 2.1986 2.600 2.264 2.535<br />

Gene number<br />

A. nidulans<br />

MG03048.4 MG10319.4 MG02978.4 MG01441.4 MG02630.4<br />

LG III III III (MAT-2) II III<br />

Supercontig 5 5 5 4 5<br />

Contig 1.80 1.81 1.80 1.63 1.83<br />

Gene number AN4745.2 AN4780.2 AN4734.2 AN3904.2 AN4853.2<br />

tical to the one present in the model organism<br />

C. heterostrophus, the genomic context of the M.<br />

graminicola MAT locus is different from that of C.<br />

heterostrophus, <strong>and</strong> appears to more closely resemble<br />

the Sordariomycete structure. Three genes were<br />

identified in the region 5 ′ of MAT1-2: APN2, APC5,<br />

<strong>and</strong> a putative homolog of the palI gene of A. nidulans<br />

(Waalwijk et al. 2002; Fig. 15.3). This difference<br />

from C. heterostrophus may be related to the taxonomic<br />

distance between these two species, since M.<br />

graminicola <strong>and</strong> Cochliobolus spp. are members of<br />

different, albeit sister clades, i.e., the Dothideales<br />

<strong>and</strong> Pleosporales, respectively (Liu <strong>and</strong> Hall 2004).<br />

2. MAT Context in Sordariomycetes<br />

<strong>and</strong> Eurotiomycetes<br />

The MAT context in Ascomycetes was investigated<br />

first by Butler et al. (2004) in different yeasts<br />

<strong>and</strong> N. crassa. These authors observed that the<br />

MAT locus of Yarrowia lipolytica lies between the<br />

homologs of S. cerevisiae APN2 <strong>and</strong> SLA2, two<br />

genes that were identified in the left <strong>and</strong> right<br />

flanking sequences of N. crassa. This common<br />

structure led the authors to propose that this<br />

configuration may be the ancestral one for all<br />

Ascomycetes. We have compiled the genomic sequences<br />

available from the Broad Institute (http://<br />

www.broad.mit.edu/resources.html) <strong>and</strong> from the<br />

Podospora Genome Project(http://podospora.igmo<br />

rs.u-psud.fr/) to extend the comparison to other<br />

Euascomycetes. The results are reported in<br />

Fig. 15.3. Remarkably, homologs of APN2 <strong>and</strong><br />

SLA2 were found on each side of the MAT locus<br />

in all Sordariomycetes. SLA2 <strong>and</strong> APN2 are<br />

also linked to E. nidulans MAT-1 <strong>and</strong> MAT-2,<br />

respectively. Overall, these data support the hypothesis<br />

of Butler et al. (2004). Several additional

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