Chuang Ying-Chih, Behringer Megan G, Patton Gillian, Bird Jordan T, Love Crystal E, Dalia Ankur, McKinlay James B
Department of Biology, Indiana University, Bloomington, IN, USA.
Biochemistry Program, Indiana University, Bloomington, IN, USA.
bioRxiv. 2024 Aug 19:2024.08.19.608702. doi: 10.1101/2024.08.19.608702.
Gene loss is expected in microbial communities when the benefit of obtaining a biosynthetic precursor from a neighbor via cross-feeding outweighs the cost of retaining a biosynthetic gene. However, gene cost primarily comes from expression, and many biosynthetic genes are only expressed when needed. Thus, one can conversely expect cross-feeding to repress biosynthetic gene expression and promote gene retention by lowering gene cost. Here we examined long-term bacterial cocultures pairing and for evidence of gene loss or retention in response to cross-feeding of non-essential adenine. Although continued to externalize adenine in long-term cultures, did not accumulate mutations in purine synthesis genes, even after 700 generations. purine synthesis gene expression was low in coculture, suggesting that gene repression removed selective pressure for gene loss. In support of this explanation, also had low transcript levels for iron-scavenging siderophore genes in coculture, likely because facilitated iron acquisition by . siderophore gene mutations were correspondingly rare in long-term cocultures but were prevalent in monocultures where transcript levels were high. Our data suggests that cross-feeding does not always drive gene loss, but can instead promote gene retention by repressing costly expression.
当通过交叉喂养从邻居那里获得生物合成前体的益处超过保留生物合成基因的成本时,预计微生物群落中会发生基因丢失。然而,基因成本主要来自表达,而且许多生物合成基因仅在需要时才表达。因此,相反地,可以预期交叉喂养会通过降低基因成本来抑制生物合成基因的表达并促进基因保留。在这里,我们研究了长期的细菌共培养物配对 和 ,以寻找因非必需腺嘌呤的交叉喂养而导致基因丢失或保留的证据。尽管 在长期培养中持续向外分泌腺嘌呤,但 即使在700代后,嘌呤合成基因也没有积累突变。 在共培养中嘌呤合成基因的表达较低,这表明基因抑制消除了基因丢失的选择压力。为支持这一解释, 在共培养中铁载体基因的转录水平也较低,这可能是因为 通过 促进了铁的获取。 在长期共培养中, 铁载体基因突变相应地很少见,但在转录水平较高的单培养中却很普遍。我们的数据表明,交叉喂养并不总是导致基因丢失,反而可以通过抑制高成本的表达来促进基因保留。