基于无人机低空遥感的荒漠植被覆盖度与归一化植被指数验证及其对水热梯度的响应

为了验证在荒漠地区MODIS-NDVI产品的精度以及为在气候变化背景下荒漠草地的科学管理提供依据,本文利用无人机低空遥感研究了干旱荒漠地区植被覆盖度(FVC)和归一化植被指数(NDVI)对水、热梯度的响应规律。在内蒙古阿拉善荒漠地区的100个样点采用GreenSeeker手持光谱仪获得NDVI值(NDVI_R),通过MODIS-NDVI数据产品提取每个样点的NDVI(NDVI_M),借助NDVI_R验证NDVI_M的精确度;通过无人机遥感手段获得每个采样点的FVC(FVC_U),利用像元二分模型反演每个样点的FVC(FVC_M),借助FVC_U验证FVC_M的精确度;并结合气象数据探讨基于无人机低空遥感的荒漠地区FVC和NDVI对水热梯度的响应。结果表明: MODIS-NDVI数据产品能够反映阿拉善地区的NDVI,精确度为84.2%,但比真实值高15.7%;FVC_M能够反映阿拉善地区的FVC状况,精确度为83.1%,但比真实值低14.8%;不同采集方式获得的NDVI受气象因子的影响程度不同,NDVI不仅受气温和降雨的影响,也受地温、蒸发量以及两者相互作用的影响,由于受大气影响程度不同, NDVI_M受地温、蒸发量、降水量的影响比NDVI_R大,NDVI_R受气温的影响比NDVI_M大。在阿拉善地区研究FVC随水热梯度的变化不仅要考虑降水量和气温,还应考虑蒸发量、地温以及气象因子之间相互作用的影响,其中,气温与降雨、蒸发量与地温以及气温与蒸发量之间相互作用对FVC_U的影响较大。     

Cell engineering method using fluorogenic oligonucleotide signaling probes and flow cytometry

Objective

Chromovert® Technology is presented as a new cell engineering technology to detect and purify living cells based on gene expression.

Methods

The technology utilizes fluorogenic oligonucleotide signaling probes and flow cytometry to detect and isolate individual living cells expressing one or more transfected or endogenously-expressed genes.

Results

Results for production of cell lines expressing a diversity of ion channel and membrane proteins are presented, including heteromultimeric epithelial sodium channel (αβγ-ENaC), sodium voltage-gated ion channel 1.7 (NaV1.7-αβ1β2), four unique γ-aminobutyric acid A (GABA_A) receptor ion channel subunit combinations α1β3γ2s, α2β3γ2s, α3β3γ2s and α5β3γ2s, cystic fibrosis conductance regulator (CFTR), CFTR-Δ508 and two G-protein coupled receptors (GPCRs) without reliance on leader sequences and/or chaperones. In addition, three novel plasmid-encoded sequences used to introduce 3′ untranslated RNA sequence tags in mRNA expression products and differentially-detectable fluorogenic probes directed to each are described. The tags and corresponding fluorogenic signaling probes streamline the process by enabling the multiplexed detection and isolation of cells expressing one or more genes without the need for gene-specific probes.

Conclusions

Chromovert technology is provided as a research tool for use to enrich and isolate cells engineered to express one or more desired genes.

     

SANS (USH1G) regulates pre-mRNA splicing by mediating the intra-nuclear transfer of tri-snRNP complexes

Splicing is catalyzed by the spliceosome, a compositionally dynamic complex assembled stepwise on pre-mRNA. We reveal links between splicing machinery components and the intrinsically disordered ciliopathy protein SANS. Pathogenic mutations in SANS/USH1G lead to Usher syndrome—the most common cause of deaf-blindness. Previously, SANS was shown to function only in the cytosol and primary cilia. Here, we have uncovered molecular links between SANS and pre-mRNA splicing catalyzed by the spliceosome in the nucleus. We show that SANS is found in Cajal bodies and nuclear speckles, where it interacts with components of spliceosomal sub-complexes such as SF3B1 and the large splicing cofactor SON but also with PRPFs and snRNAs related to the tri-snRNP complex. SANS is required for the transfer of tri-snRNPs between Cajal bodies and nuclear speckles for spliceosome assembly and may also participate in snRNP recycling back to Cajal bodies. SANS depletion alters the kinetics of spliceosome assembly, leading to accumulation of complex A. SANS deficiency and USH1G pathogenic mutations affects splicing of genes related to cell proliferation and human Usher syndrome. Thus, we provide the first evidence that splicing dysregulation may participate in the pathophysiology of Usher syndrome.     

Integrated Microarray to Identify the Hub miRNAs and Constructed miRNA–mRNA Network in Neuroblastoma Via Bioinformatics Analysis

Neurochemical Research - Neuroblastomas (NB) are childhood malignant tumors originating in the sympathetic nervous system. MicroRNAs (miRNAs) play an essential regulatory role in tumorigenesis and...