Correlation between the compact regions predicted by the Average Distance Map (ADM) and the biologically active sites in atrial natriuretic peptide

The prediction of the short-range compact regions of human atrial natriuretic peptide (a-hANP), one of the biologically active peptides, has been made by means of the Average Distance Map(ADM). We found out that the location of the predicted short-range compact regions is consistent with the structural units determined by the NMR analysis (Kobayashiet al., 1988). Furthermore, the short-range compact regions correspond well to the biologically active areas of atriopeptin (103–125)-amide (which is homologous peptide toa-hANP), detected by the glycine substitution technique (Konishiet al., 1987). The results suggest that a predicted short-range compact region can be regarded as a possible active site in a biologically active peptide.     

Repetitive DNA in and around translocation breakpoints of the Philadelphia chromosome

This paper describes systematic sequence studies of repetitive DNA in and around translocation breakpoints on chromosomes 9 and 22, which are involved in the formation of the Philadelphia chromosome in acute leukemias. In addition to Alu repeats described in previous studies, the breakpoint regions appear to contain many other repetitive elements, including a member of a new repetitive family (MER34) reported in this paper. Identification of these repeats broadens current studies on the possible involvement of repetitive DNA in this intensely studied chromosomal translocation.     

Distinct functions of maternal and somatic Pat1 protein paralogs

We previously identified Xenopus Pat1a (P100) as a member of the maternal CPEB RNP complex, whose components resemble those of P-(rocessing) bodies, and which is implicated in translational control in Xenopus oocytes. Database searches have identified Pat1a proteins in other vertebrates, as well as paralogous Pat1b proteins. Here we characterize Pat1 proteins, which have no readily discernable sequence features, in Xenopus oocytes, eggs, and early embryos and in human tissue culture cells. xPat1a and 1b have essentially mutually exclusive expression patterns in oogenesis and embryogenesis. xPat1a is degraded during meiotic maturation, via PEST-like regions, while xPat1b mRNA is translationally activated at GVBD by cytoplasmic polyadenylation. Pat1 proteins bind RNA in vitro, via a central domain, with a preference for G-rich sequences, including the NRAS 5′ UTR G-quadruplex-forming sequence. When tethered to reporter mRNA, both Pat proteins repress translation in oocytes. Indeed, both epitope-tagged proteins interact with the same components of the CPEB RNP complex, including CPEB, Xp54, eIF4E1b, Rap55B, and ePAB. However, examining endogenous protein interactions, we find that in oocytes only xPat1a is a bona fide component of the CPEB RNP, and that xPat1b resides in a separate large complex. In tissue culture cells, hPat1b localizes to P-bodies, while mPat1a-GFP is either found weakly in P-bodies or disperses P-bodies in a dominant-negative fashion. Altogether we conclude that Pat1a and Pat1b proteins have distinct functions, mediated in separate complexes. Pat1a is a translational repressor in oocytes in a CPEB-containing complex, and Pat1b is a component of P-bodies in somatic cells.     

京津冀地区新型城镇化对土地生态效率影响的实证分析

近年来, 城市化进程的不断推进对城市土地利用及生态环境产生了极大影响。选取城镇化发展最为迅速与典型的京津冀地区作为研究区域, 采用超效率DEA模型及Malmquist效率指数, 从经济学角度分析2006-2015年土地生态效率的时空演变, 随后, 基于人口、富裕和技术(STRIPAT)模型, 构建新型城镇化发展水平的综合指标评价体系, 分析新型城镇化对土地生态效率的影响。研究结果表明: 京津冀地区城镇化发展水平与土地生态效率之间存在显著的正相关关系, 即城镇化水平的不断提升对土地生态效率的提高具有积极作用, 各城市土地生态效率在新型城镇化发展背景下存在明显的空间差异, 此外, 土地利用与管理技术水平的提高、环境政策的改变等均会对土地生态效率的提升产生积极影响。这项研究旨在为提高城市土地管理水平, 推动城市可持续发展提供决策支持。     

Occurrence frequencies and regional variations in Visible Infrared Imaging Radiometer Suite (VIIRS) global active fires

Active fires are considered to be the key contributor to, and critical consequence of, climate change. Quantifying the occurrence frequency and regional variations in global active fires is significant for assessing carbon cycling, atmospheric chemistry, and postfire ecological effects. Multiscale variations in fire occurrence frequencies have still never been fully investigated despite free access to global active fire products. We analyzed the occurrence frequencies of Visible Infrared Imaging Radiometer Suite (VIIRS) active fires at national, pan‐regional (tropics and extratropics) to global scales and at hourly, monthly, and annual scales during 2012–2017. The results revealed that the accumulated occurrence frequencies of VIIRS global active fires were up to 12,193 × 10⁴, yet exhibiting slight fluctuations annually and with respect to the 2014–2016 El Niño event, especially during 2015. About 35.52% of VIIRS active fires occurred from July to September, particularly in August (13.06%), and typically between 10:00 and 13:00 Greenwich Mean Time (GMT; 42.96%) and especially at 11:00 GMT (17.65%). The total counts conform to a bimodal pattern with peaks in 5°–11°N (18.01%) and 5°–18°S (32.46%), respectively, alongside a unimodal distribution in terms of longitudes between 15°E and 30°E (32.34%). Tropical annual average of active fire (1,496.81 × 10⁴) accounted for 75.83%. Nearly 30% were counted in Brazil, the Democratic Republic of the Congo, Indonesia, and Mainland Southeast Asia (MSEA). Fires typically occurred between June (or August) and October (or November) with far below‐average rainfall in these countries, while those in MSEA primarily occurred between February and April during the dry season. They were primarily observed between 00:00 and 02:00 GMT, between 12:00 and 14:00 within each Zone Time. We believed that VIIRS global active fires products are useful for developing fire detection algorithms, discriminating occurrence types and ignition causes via correlation analyses with physical geographic elements, and assessment of their potential impacts.     

Intrinsic disorder in protein sense‐antisense recognition

In addition to the well‐established sense‐antisense complementarity abundantly present in the nucleic acid world and serving as a basic principle of the specific double‐helical structure of DNA, production of mRNA, and genetic code‐based biosynthesis of proteins, sense‐antisense complementarity is also present in proteins, where sense and antisense peptides were shown to interact with each other with increased probability. In nucleic acids, sense‐antisense complementarity is achieved via the Watson‐Crick complementarity of the base pairs or nucleotide pairing. In proteins, the complementarity between sense and antisense peptides depends on a specific hydropathic pattern, where codons for hydrophilic and hydrophobic amino acids in a sense peptide are complemented by the codons for hydrophobic and hydrophilic amino acids in its antisense counterpart. We are showing here that in addition to this pattern of the complementary hydrophobicity, sense and antisense peptides are characterized by the complementary order‐disorder patterns and show complementarity in sequence distribution of their disorder‐based interaction sites. We also discuss how this order‐disorder complementarity can be related to protein evolution.