Linker histone protein variants are expressed in different tissues, at various developmental stages or induced by specific environmental conditions in many plant species. In most cases, the function of these proteins remains unknown. In the work presented here an antisense strategy has been used to study the function of the drought-induced linker histone, H1-S of tomato. Three independent H1-S antisense tomato mutants, selected for their inability to accumulate H1-S in response to water stress, were studied. These mutants have been characterized at the physiological and morphological levels. Histone H1-S antisense transgenic plants developed normally indicating that H1-S does not play an important role in the basal functions of tomato development. No differences were detected in chromatin organization, excluding a structural role for H1-S in chromatin organization. However, differences between the wild-type and antisense plants were observed in leaf anatomy and physiological activities. This analysis indicates that H1-S has more than one function, at different times, in controlling plant water status, highlighting the complexity of the water stress response.

The uniqueness of the cpDNA haplotypes, the prevalence of clonality and the restricted number of genets recorded suggest that Sardinian white poplar could be a floristic relict of the native flora of the island, which has spread through available habitats on the island mainly by means of vegetative propagation and human activities.

Morphological traits traditionally adopted to discriminate between Populus alba L. and P. tremula L. have frequently led to misclassification of their spontaneous hybrid P. · canescens Sm. Moreover, they may not be of any help in cases of spontaneous backcross phenomena. These limitations can be overcome by molecular markers, which are not environmentally influenced nor subjectively assessed. In this study, the effectiveness of amplified fragment length polymorphism (AFLP) and simple sequence repeat (SSR) markers in species and hybrid discrimination was evaluated by analysing a set of reference samples of P. alba,P. tremula and P. · canescens. Species-specific and speciesindicative AFLPs, as well as diagnostic SSR alleles, were recorded in both P. alba and P. tremula reference samples. The results allowed a clear distinction between the two poplar species and their hybrid. Using these diagnostic markers, a natural population of P. alba trees sampled along the Ticino river basin in northern Italy was analysed, and P. · canescens individuals, intermingled with P. alba trees, were detected.

No abstract

White poplar ( Populus alba ) is a widespread species of the northern hemisphere. Introgressed populations or hybrid zones with the related species of the European aspen ( Populus tremula ) have been suggested as potential venues for the identification of functionally important variation for germplasm conservation, restoration efforts and tree breeding. Data on the genetic diversity and structure of introgressed P. alba are available only for sympatric populations from central Europe. Here, clonality, introgression and spatial genetic patterns were evaluated in three riparian populations of P. alba along the Ticino, Paglia-Tevere and Cesano river drainages in Italy. Samples of all three populations were typed for five nuclear microsatellite markers and 137 polymorphic amplified fragment length polymorphisms. Microsatellite-based inbreeding co-efficients ( F IS ) were significantly positive in all three populations. Genetic diversity was consistently highest in Ticino, the population with the highest level of introgression from P. tremula . Population differentiation ( F ST ) was low between the Ticino valley in northern Italy and the Cesano valley in central Italy and between the central Italian populations of Cesano and Paglia-Tevere, consistent with a role of the Appenine mountain range as a barrier to gene flow between adjacent drainage areas. Introgression was not the primary determinant of within-population spatial genetic structure (SGS) in the studied populations.