|Table of Contents|

Mating-type Molecular Identification of Phlebopus portentosus Homokaryotic Strains

《北方园艺》[ISSN:1001-0009/CN:23-1247/S]

Issue:
2024年22
Page:
101-108
Research Field:
Publishing date:

Info

Title:
Mating-type Molecular Identification of Phlebopus portentosus Homokaryotic Strains
Author(s):
CAO Yang123LUO Shunzhen1HE Chunmei1JI Guangyan1SHU Ping3JI Kaiping12
(1.Jinghong Hongzhen Agricultural Science and Technology Co.Ltd.,Jinghong,Yunnan 666100;2.Guizhou Hongzhen Fungus Industry Investment and Development Co.Ltd.,Zhenfeng,Guizhou 562200;3.Dali Comprehensive Inspection Centre of Quality and Technical Supervision,Dali,Yunnan 671000)
Keywords:
Phlebopus portentosusmating-typeidentificationSNP marker
PACS:
S 646.3
DOI:
10.11937/bfyy.20241213
Abstract:
Heterokaryotic parent strains and their offspring homokaryotic strains of Phlebopus portentosus were used as the test materials.β-flanking gene and ste3.2 gene,which respectively represent mating-type A and B genotype,was used to develop molecular markers to study the mating-type identification of P.portentosus homokaryotic strains,in order to provide reference for improving the work efficiency of its cross breeding.The results showed that 5 pairs the primers could amplify 91% of the β-flanking gene region,other 5 pairs could amplify 71% of the ste3.2 gene region.Amplification sequencing was successfully performed on 2 heterokaryotic parent strains using all primers above although the usable sequence lengths and SNP sites numbers were visibly different.Based on the results of first round PCR,primers beta2 and 3.22 were chosen for the second round PCR and mating-typing of HZ19110 homokaryotic strains.There were 5,4,4 and 4 homokaryotic strains of mating-type A1B1,A2B2,A1B2,and A2B1 respectively.Primers beta5 and 3.25 were chosen for the second round PCR and mating-typing of HZ20029 homokaryotic strains.There were 4,3,3 and 3 homokaryotic strains of mating-type A3B3,A4B4,A3B4,and A4B3 respectively.The mating-type identification of homokaryotic strains was consistent with the results of pairwise culture and clamp screening under microscope.Mating-type of P.portentosus homokaryotic strains from different heterokaryotic parent strains could be rapidly and accurately identified by using the molecular methods in this study.The breeding efficiency of this species could be consequently improved.

References:

[1]HEINEMANN P,RAMMELOO J.Observations sur le genre Phlebopus (Boletineae)[J].Mycotaxon,1982(15):384-404.[2]SEGEDIN B P.An annotated checklist of Agarics and Boleti recorded from New Zealand[J].New Zealand Journal of Botany,1987,25(2):185-215.[3]WATLING R.The relationships and possible distributional patterns of boletes in south-east Asia[J].Mycological Research,2001,105(12):1440-1448.[4]BANDALA V M,MONTOYA L,JARVIO D.Two interesting records of boletes found in coffee plantations in Eastern Mexico[J].Persoonia,2004,18(3):365-380.[5]杨祝良,臧穆.中国南部高等真菌的热带亲缘[J].云南植物研究,2003,25(2):129-144.[6]臧穆.中国真菌志(第22卷):牛肝菌科1[M].北京:科学出版社,2006.[7]曹旸,纪光燕,罗顺珍,等.暗褐网柄牛肝菌人工驯化研究的回顾与前瞻[J].菌物学报,2021,40(12):3064-3080.[8]曹旸,方艺伟,高锋,等.暗褐网柄牛肝菌交配系统研究[J].北方园艺,2016(24):133-135.[9]CAO Y,ZHANG Y,YU Z,et al.Genome sequence of Phlebopus portentosus strain PP33,a cultivated bolete[J].Genome Announcements,2015,3(2):e00326-15.[10]CAMACHO C,COULOURIS G,AVAGYAN V,et al.BLAST+:Architecture and applications[J].BMC Bioinformatics,2009,10:421.[11]HALL T.Bioedit:A user-friendly biological sequence alignment editor and analysis program for windows 95/98/NT[J].Nucleic Acids Symposium Series,1999,41:95-98.[12]THOMPSON J D,GIBSON T J,PLEWNIAK F,et al.The CLUSTAL_X windows interface:Flexible strategies for multiple sequence alignment aided by quality analysis tools[J].Nucleic Acids Research,1997,25(24):4876-4882.[13]KUMAR S,STECHER G,LI M,et al.MEGA X:Molecular evolutionary genetics analysis across computing platforms[J].Molecular Biology and Evolution,2018,35(6):1547-1549.[14]鲍大鹏.担子菌类食用真菌双核体生物学性质研究进展及其启迪[J].菌物学报,2024,43(4):14-29.[15]张芳芳,陈雪凤,张雯龙,等.香菇单核体交配型及杂交后代的等位基因特异性PCR鉴定[J].微生物学通报,2024,51(5):1741-1753.[16]王丽宁,黄清铧,李锦荣.用于鉴定灵芝原生质体单核体交配型的引物对、试剂盒及其应用[P].中国:CN112126700A.2020-12-25.[17]果禹鑫,陈青君,张国庆,等.运用交配型基因分子标记辅助羊肚菌单孢杂交育种[J].分子植物育种,2022,20(12):4067-4074.[18]陈浩然,李忻洋,刘珍,等.蛹虫草单孢菌株的生物学特性及稳定性[J].菌物学报,2023,42(9):1918-1928.[19]陈卫民,柴红梅,杨玮娴,等.柱状田头菇和杨柳田头菇B交配型位点特征分析及其应用[J].生物技术通报,2021,37(11):57-64.[20]周金看,杨瑶,冯璠,等.不同杏鲍菇品种种质鉴定及原生质体单核体杂交育种[J].北方园艺,2023(24):118-125.[21]李慧,夏伟伟,胡子钰,等.利用ISSR-SCAR标记鉴定金针菇双-单杂交子[J].北方园艺,2022(16):121-127.

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Last Update: 2024-12-03