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Cloning of the Lentinula edodes B mating-type locus and identification of the genetic structure controlling B mating
Authors:Lin Wu  Arend van Peer  Wenhua Song  Hong Wang  Mingjie Chen  Qi Tan  Chunyan Song  Meiyan Zhang  Dapeng Bao
Affiliation:1. Institute of Edible Fungi, Shanghai Academy of Agricultural Sciences, Shanghai, P.R. China;2. Iwate Biotechnology Research Center, Iwate, Japan;3. Key Laboratory of Edible Fungi Resources and Utilization (South), Ministry of Agriculture, P.R. China;4. National Engineering Research Center of Edible Fungi, Ministry of Science and Technology, P.R. China
Abstract:During the life cycle of heterothallic tetrapolar Agaricomycetes such as Lentinula edodes (Berk.) Pegler, the mating type system, composed of unlinked A and B loci, plays a vital role in controlling sexual development and resulting formation of the fruit body. L. edodes is produced worldwide for consumption and medicinal purposes, and understanding its sexual development is therefore of great importance. A considerable amount of mating type factors has been indicated over the past decades but few genes have actually been identified, and no complete genetic structures of L. edodes B mating-type loci are available. In this study, we cloned the matB regions from two mating compatible L. edodes strains, 939P26 and 939P42. Four pheromone receptors were identified on each new matB region, together with three and four pheromone precursor genes in the respective strains. Gene polymorphism, phylogenetic analysis and distribution of pheromone receptors and pheromone precursors clearly indicate a bipartite matB locus, each sublocus containing a pheromone receptor and one or two pheromone precursors. Detailed sequence comparisons of genetic structures between the matB regions of strains 939P42, 939P26 and a previously reported strain SUP2 further supported this model and allowed identification of the B mating type subloci borders. Mating studies confirmed the control of B mating by the identified pheromone receptors and pheromones in L. edodes.
Keywords:AA, amino acid(s)   AF, aliphatic amino acids (or alanine)&ndash  phenylalanine   bp, base pair(s)   CAAX, cysteine&ndash  aliphatic amino acids&ndash  aliphatic amino acids&ndash  any residue   Cc, Coprinopsis cinerea   CIIA, cysteine&ndash  isoleucine&ndash  isoleucine&ndash  alanine   CIIS, cysteine&ndash  isoleucine&ndash  isoleucine&ndash  serine   CVIL, cysteine&ndash  valine&ndash  isoleucine&ndash  leucine   CVIS, cysteine&ndash  valine&ndash  isoleucine&ndash  serine   CVVA, cysteine&ndash  valine&ndash  valine&ndash  alanine   Cn, Cryptococcus neoformans   CTAB, Cetyltrimethyl Ammonium Bromide   DDE, aspartic acid&ndash  aspartic acid&ndash  glutamic acid   dNTP, deoxyribonucleoside triphosphate   E/A, glutamic acid/alanine   E/H, glutamic acid/histidine   ER, glutamic acid&ndash  arginine   Fv, Flammulina velutipes   GF, glycine&ndash  phenylalanine   GY, glycine&ndash  tyrosine   GX, glycine&ndash  any residue   kb, kilobase(s) or 1000   bp   Le, Lentinula edodes   Lb, Laccaria bicolor   NCBI, National Center for Biotechnology Information   No, number   PCR, polymerase chain reaction   PDA, Potato, Dextrose and Agar medium   PDY, Potato, Dextrose and Yeast extract medium   PXD, proline&ndash  any residue&ndash  aspartic acid   PXN, proline&ndash  any residue&ndash  aspartic acid&ndash  asparaginate   TM, transmembrane   XF, any residue&ndash  phenylalanine
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