co.ton is the most widely cultivated co.mercial crop producing natural fiber around the *** a critical trait for fiber quality,fiber strength principally determined during the seco.dary wall thickening *** on the deve...
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co.ton is the most widely cultivated co.mercial crop producing natural fiber around the *** a critical trait for fiber quality,fiber strength principally determined during the seco.dary wall thickening *** on the developed BC5F3:5 CSSLs(chromosome segment substitution lines)from Gossypium hirsutum CCRI36×*** Hai 1,the superior MBI9915 was chosen to co.struct the seco.dary segregated population BC7F2 with its recurrent parent CCRI36,which was subsequently subjected to Bulk segregant RNA-sequencing(BSR-seq)for rapid identification of candidate genes related to fiber strength.A total of 4 fiber-transcriptome libraries were separately co.structed and sequenced,including two parents(CCRI36 and MBI9915)and two extreme pools at 20 DPA(days post anathesis).Through multiple co.parisons,536 DEGs(differentially expressed genes)were overlapped at 20 ***-polymorphism co.parison in mRNA sequences revealed 831 highly probable SNPs between two extreme pools related to fiber *** analysis was performed between two extreme pools with SNP-index *** co.related regions with 1981 annotation genes were obtained between two pools at 20 DPA,of which 12 co.mon DEGs were similarly identified both between two parents and two *** gene(Gh_A07G0837)in the candidate region related to fiber strength was differentially expressed in both parents and extreme pools and involved in fiber strength development through reactive oxygen species(ROS)***-expression analysis of Gh_A07G0837 showed that Gh_A07G0837 may co.perate with other genes to regulate fiber *** reliability of BSR-seq results was validated by the quantitative real-time PCR(qRT-PCR)experiments on 5 co.mon DGEs 20 ***-expressed analysis results indicated that there were some genes expressed especially low in MBI9915,resulting in good fiber *** on bulked segregant analysis on the extreme pools derived from superior CSSL population,this study indicates
The accessory olfactory bulb(AOB), located at the posterior dorsal aspect of the main olfactory bulb(MOB), is the first brain relay of the accessory olfactory system(AOS), which can parallelly detect and process volat...
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The accessory olfactory bulb(AOB), located at the posterior dorsal aspect of the main olfactory bulb(MOB), is the first brain relay of the accessory olfactory system(AOS), which can parallelly detect and process volatile and nonvolatile social chemosignals and mediate different sexual and social behaviors with the main olfactory system(MOS). However, due to its anatomical location and absence of specific markers, there is a lack of research on the internal and external neural circuits of the AOB. This issue was addressed by singleco.or labeling and fluorescent double labeling using retrograde rAAVs injected into the bed nucleus of the stria terminalis(BST), anterior co.tical amygdalar area(Aco., medial amygdaloid nucleus(MeA), and posteromedial co.tical amygdaloid area(PMco. in mice. We demonstrated the effectiveness of this AOB projection neuron labeling method and showed that the mitral cells of the AOB exhibited efferent projection dispersion characteristics similar to those of the MOB. Moreover, there were significant differences in the number of neurons projected to different brain regions, which indicated that each mitral cell in the AOB co.ld project to a different number of neurons in different co.tices. These results provide a circuitry basis to help understand the mechanism by which pheromone information is enco.ed and deco.ed in the AOS.
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