scholarly journals Targeted Sequence Capture Provides Insight into Genome Structure and Genetics of Male Sterility in a Gynodioecious Diploid Strawberry, Fragaria vesca ssp. bracteata (Rosaceae)

2013 ◽  
Vol 3 (8) ◽  
pp. 1341-1351 ◽  
Author(s):  
Jacob A. Tennessen ◽  
Rajanikanth Govindarajulu ◽  
Aaron Liston ◽  
Tia-Lynn Ashman
2015 ◽  
Author(s):  
Tia-Lynn Ashman ◽  
Jacob Tennessen ◽  
Rebecca Dalton ◽  
Rajanikanth Govindarajulu ◽  
Mathew Koski ◽  
...  

Gynodioecy, the coexistence of females and hermaphrodites, occurs in 20% of angiosperm families and often enables transitions between hermaphroditism and dioecy. Clarifying mechanisms of sex determination in gynodioecious species can thus illuminate sexual system evolution. Genetic determination of gynodioecy, however, can be complex and is not fully characterized in any wild species. We used targeted sequence capture to genetically map a novel nuclear contributor to male sterility in a self-pollinated hermaphrodite of Fragaria vesca subsp. bracteata from the southern portion of its range. To understand its interaction with another identified locus and possibly additional loci, we performed crosses within and between two populations separated by 2000 km, phenotyped the progeny and sequenced candidate markers at both sex-determining loci. The newly mapped locus contains a high density of pentatricopeptide repeat genes, a class commonly involved in restoration of fertility caused by cytoplasmic male sterility. Examination of all crosses revealed three unlinked epistatically interacting loci that determine sexual phenotype and vary in frequency between populations. Fragaria vesca subsp. bracteata represents the first wild gynodioecious species with genomic evidence of both cytoplasmic and nuclear genes in sex determination. We propose a model for the interactions between these loci and new hypotheses for the evolution of sex determining chromosomes in the subdioecious and dioecious Fragaria.


2020 ◽  
Author(s):  
Ting Wang ◽  
Qingshan Chen ◽  
Longhao Kuang ◽  
Jiantao Wang ◽  
Xiaohe Yan

Abstract Background: Bietti crystalline corneoretinal dystrophy (BCD) is an autosomal recessive retinal dystrophy which is caused by the mutations of CYP4V2.Here we identified new CYP4V2compound heterozygous mutations in BCD.Methods:381 pathogenic genes related to retinal diseases were screened by targeted sequence capture array techniques and confirmed by Sanger sequencing.Results:Two female siblings with BCD carry two compound heterozygous mutations in CYP4V2. One was missense mutation c.1198C>T (p.R400C) and the other was frameshift mutation c.802-8_810delinsGC (p.V268_E329del).Optical coherence tomography (OCT) showed that the ellipsoid zone was absent in the macular regions and electroretinogram (ERG) revealed poor cone and rod responses. Conclusions:Newcompound heterozygous mutations in CYP4V2 are related to the BCD.Our study expands our knowledge of heterogenic phenotypes and genotypes through genetic diagnosis of the BCD patients.


2019 ◽  
Vol 20 (3) ◽  
pp. 578 ◽  
Author(s):  
Peng Wang ◽  
Qiaohua Lu ◽  
Yixin Ai ◽  
Yihao Wang ◽  
Tiantian Li ◽  
...  

Cytoplasmic male sterility (CMS), which is controlled by mitochondrial genes, is an important trait for commercial hybrid seed production. So far, genes controlling this trait are still not clear in pepper. In this study, complete mitochondrial genomes were sequenced and assembled for the CMS line 138A and its maintainer line 138B. The genome size of 138A is 504,210 bp, which is 8618 bp shorter than that of 138B. Meanwhile, more than 214 and 215 open reading frames longer than 100 amino acids (aas) were identified in 138A and 138B, respectively. Mitochondrial genome structure of 138A was quite different from that of 138B, indicating the existence of recombination and rearrangement events. Based on the mitochondrial genome sequence and structure variations, mitochondrion of 138A and FS4401, a Korean origin CMS line, may have inherited from a common female ancestor, but their CMS traits did originate separately. Candidate gene selection was performed according to the published characteristics of the CMS genes, including the presence SNPs and InDels, located in unique regions, their chimeric structure, co-transcription, and transmembrane domain. A total of 35 ORFs were considered as potential candidate genes and 14 of these were selected, with orf300a and 0rf314a as strong candidates. A new marker, orf300a, was developed which did co-segregate with the CMS trait.


2020 ◽  
Vol 8 (10) ◽  
Author(s):  
Brian J. Sanderson ◽  
Stephen P. DiFazio ◽  
Quentin C. B. Cronk ◽  
Tao Ma ◽  
Matthew S. Olson

2015 ◽  
Vol 43 (6) ◽  
pp. 3389-3404 ◽  
Author(s):  
Henriette O'Geen ◽  
Isabelle M. Henry ◽  
Mital S. Bhakta ◽  
Joshua F. Meckler ◽  
David J. Segal

2019 ◽  
Vol 20 (1) ◽  
pp. 140-153 ◽  
Author(s):  
Laurel R. Yohe ◽  
Kalina T. J. Davies ◽  
Nancy B. Simmons ◽  
Karen E. Sears ◽  
Elizabeth R. Dumont ◽  
...  

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