Late replicating bands of human chromosomes demonstrated by fluorochrome and Giemsa staining.

The addition of thymidine (TdR) to cells growing in a medium containing 5-bromodeoxyuridine (BUdR) at the end of the first replication cycle results in the incorporation of TdR into the late replicating DNA regions. These sites can be visualized by staining the metaphase chromosomes with the fluorescent dye "33258 Hoechst" or a "33258 Hoechst" Giemsa procedure. A sequence of late replication patterns has been established in metaphase chromosomes of cultured human peripheral lymphocytes. The patterns are in agreement with those obtained by the standard autoradiographic procedures, but are more accurate. As is known from autoradiography, late replicating bands are in the position of G or Q bands. The "33258 Hoechst" Giemsa staining procedure of chromosomes which have replicated in the presence of BUdR first and in TdR for the last 2 hrs of the S phase is preferable to the currently used Giemsa banding techniques: the method yields very well banded metaphases in all preparations examined, as the chromosome structure is not disrupted by the pretreatment. The bands are very distinct, even in the "difficult" chromosomes (e.g. No. 4, 5, 8 and X). In female cells the late replicating X chromosome can be identified by its size and staining pattern. In addition to the replication asynchrony, the sequence of replication within both X chromosomes in female cells is not absolutely identical. The phenomenon of a phase difference in replication between the homologues is not a peculiarity of the X chromosome, but can be found in all autosomes as well as in homologous positions on the chromatids of individual chromosomes.     

The human transmembrane secretory component (poly-Ig receptor): molecular cloning,restriction fragment length polymorphism and chromosomal sublocalization

Summary The human transmembrane secretory component (SC) mediates glandular translocation of polymeric IgA and IgM into exocrine secretions. A 2898-bp cDNA clone, encoding the entire sequence of the human transmembrane SC, was isolated from a colonic adenocarcinoma cell line cDNA library. The deduced amino-acid sequence had a length of 764 residues and showed an overall similarity of 56% and 64% with the rabbit and rat counterpart, respectively. A restriction fragment length polymorphism (RFLP) was found with PvuII, revealing a two-alle RFLP with an autosomal codominant inheritance pattern and allele frequencies of 0.65 and 0.35. Southern blot analysis of human-rodent somatic hybrid panels, including hybrids with translocation chromosomes carrying different parts of chromosome 1, assigned the SC gene to 1q31-q42, thus confirming a previously reported provisional assignment.     

Cystic fibrosis: typing 48 German families with linked DNA probes

Summary Two hundred and thirty five subjects from 48 German cystic fibrosis (CF) families were typed for restriction fragment length polymorphisms (RFLPs) detected by the probes pmet H, pmet D, and pJ 3.11, known to be tightly linked to the CF gene. Gene and haplotype frequencies suggest a linkage disequilibrium with the CF locus. The analysis of the predictive value of this typing in individual CF families indicates that the combined use of these probes provides a powerful diagnostic system both for carrier detection and prenatal diagnosis. In 33 out of 48 families carriers and non-carriers could be identified, and in 26 of these 33 families prenatal diagnosis could discriminate between affected and unaffected offspring.     

The structural gene for transferrin (TF) maps to 3q21----3qter

A cloned human cDNA for transferrin (TF) was used as hybridization probe in analysing a series of rodent x human somatic cell hybrids for the presence of human TF sequences. The assignment to chromosome 3 was further refined to region 3q21----3qter using hybrids that carried a translocated chromosome 3 and fibroblasts from a patient trisomic for this region. The gene for TF therefore maps to the same region as the gene for transferrin receptor (TFR) thereby defining an iron transport region on 3q2 to which the transferrin-related tumor associated antigen p97 may also belong. It follows that the genes for pseudocholinesterase (CHE1), ceruleoplasmin (CP) and alpha-2HS-glycoprotein (A2HS) which belong to the, as yet unassigned, linkage group of TF, now also map to chromosome 3 in man.     

Cytovillin, a microvillar Mr 75,000 protein. cDNA sequence, prokaryotic expression, and chromosomal localization

Cytovillin is a microvillar cytoplasmic peripheral membrane protein, with prominent expression in vivo in placental syncytiotrophoblasts and certain human tumors. Cytovillin cDNA was cloned from a human placental lambda gt11 library using affinity purified antibodies. The identity of cytovillin cDNA clones was confirmed by expression of cytovillin in Escherichia coli and using antibodies raised against the expressed fusion protein in comparison with antibodies against cytovillin purified from cultured human choriocarcinoma cells. In these cells Northern blotting analysis identified a major 3.5-kilobase cytovillin mRNA. The cDNA encodes a protein of 575 amino acids corresponding to a molecular weight of 68,084. According to secondary structure prediction, cytovillin is a hydrophilic protein with an extensive internal alpha-helical region ending in a sequence of 7 consecutive prolines. The predicted alpha-helical region showed limited homology to alpha-helical regions of cytoskeletal proteins and certain other proteins, but no extensive homologies were found in the cytovillin cDNA or the deduced amino acid sequence to other registered DNA or protein sequences. Southern blot analysis of a DNA panel of human mouse somatic cell hybrids localized the cytovillin gene to the end of the long arm of chromosome 6 (6q22-q27). Our results show that cytovillin is representative of a novel class of microvillar proteins.     

锦鸡儿植物对盐碱地土壤理化性质和细菌群落的影响

锦鸡儿属的多种植物在干旱/半干旱区域水土保持等方面具有显著的作用效果,该研究以柠条锦鸡儿、中间锦鸡儿和小叶锦鸡儿为材料,选择宁夏银北西大滩核心试验站的盐渍化荒地为研究对象,分析了3种锦鸡儿建植1年对盐碱地土壤理化性质及土壤细菌群落的影响,以了解该类植物在盐碱地改良中的作用及生态效应。结果显示:(1)种植锦鸡儿1年能够显著降低盐碱地土壤全盐含量和pH,提高土壤全氮和全磷含量。(2)种植锦鸡儿不影响其非根际土壤细菌群落的α多样性,但小叶锦鸡儿非根际土壤细菌群落的香浓指数最低。(3)不同种锦鸡儿对盐碱地细菌群落结构的影响有所不同,小叶锦鸡儿根际/非根际细菌群落的结构分别与对照土壤以及柠条、中间锦鸡儿根际土壤存在明显差异;在属水平,包括假黄色单胞菌属、新鞘氨醇菌属及根瘤菌属在内的12个优势细菌属的相对丰度在小叶锦鸡儿非根际土壤中显著增加。(4)db-RDA分析表明,盐碱地土壤全盐、全氮及全磷含量分别解释了锦鸡儿非根际细菌群落结构变异信息的23.5%、25.4%和22.2%,3种因子累计共解释48.5%的细菌群落变异(P0.05),但这些因子对锦鸡儿根际细菌群落的变化无显著影响。研究表明,短期种植锦鸡儿属植物对盐碱地土壤理化性质具有一定改良效果,且不影响非根际土壤细菌群落的α多样性,但不同种锦鸡儿对土壤细菌群落结构的影响存在差异。     

土壤增温与氮添加对杉木幼苗细根径级根长分布的影响

通过在福建省三明市陈大林业国有林场内开展土壤增温(增温5 ℃、不增温)和氮添加(不添加、4、8 g N·m^-2·a^-1)的交互试验(共6个处理),研究土壤增温、氮添加及二者交互作用对杉木细根径级根长分布的影响,用扩展模型可很好地拟合6个处理的径级根长分布(R²=0.97).结果表明: 增温使杉木细根总根长变小,但对细根直径影响不显著;氮添加使杉木细根总根长和直径均变小;增温和氮添加的交互作用对细根总根长有显著影响,但对细根直径无显著影响.6个处理细根径级根长分布均能用极值函数模型较好地拟合(R²>0.98).相关分析显示,直径<1 mm细根的比根长与极值模型拟合参数c值呈显著负相关,实际总根长与极值模型拟合参数b呈显著正相关.增温和氮添加及其交互作用可以影响杉木细根形态特征;极值模型拟合各处理径级根长分布所得参数在一定程度上可以反映细根形态特征对环境条件变化的响应.     

温光条件与寒地水稻产量和源库特征的关系

采用大田试验,以寒地水稻为研究对象,分析试验区2011—2014年气温和太阳辐射,比较不同年份间温光条件差异,探讨温光条件与水稻干物质积累、源库光合特征、产量及其构成之间的关系。结果表明:生育期内日活动积温利用率和日有效积温利用率呈逐年增加的趋势,而太阳辐射呈逐年降低的趋势,其中灌浆期太阳辐射强度以2014年居高;生育期内日活动积温和日有效积温及其利用率、抽穗后日平均太阳辐射强度与粒数、结实率、千粒重以及产量显著或极显著正相关;生育期内活动积温与产量(R~2=0.69)、生物产量(R~2=0.49)、抽穗期茎鞘干质量(R~2=0.74)及粒叶比(R~2=0.34)、收获指数(R~2=0.63)、群体生长速率(R~2=0.78)和净同化率(R~2=0.73)均呈二次函数关系,且拟合效果均达极显著水平,而与叶面积指数呈极显著正相关关系(R=0.80)。     

黄土高原不同植被覆盖对流域水文的影响

以山西省吉县蔡家川流域为对象,研究了植被覆盖类型对流域水文的影响.结果表明:不同植被覆盖的流域年径流系数分别为:林地流域1.6%～2.3%,以农、牧为主的流域3.1%～3.9%;各流域基流系数差异显著,人工林流域为零,次生林为主的流域1.0%～1.5%,以农、牧为主的流域2.5%～2.8%;在雨季人工林流域的径流总量是次生林流域的3.37倍、农地流域的1.9倍,而农地流域的基流量是次生林流域的2.2倍;短历时高强度降雨条件下,人工林流域、次生林流域地表径流量分别是农地流域的10.8倍和2.2倍;在历时较长的暴雨条件下,人工林流域单位面积上的洪峰流量是农地流域的3.4倍,次生林流域的6.9倍;在长历时、大雨量条件下,农地流域的径流量是次生林流域的1.8倍.水平梯田的水源涵养功能与次生林植被相当,次生林植被的水源涵养功能远好于人工植被,在水资源短缺的黄土高原应提倡植被的自然恢复.